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  • 1995-1999  (1,651)
  • 1960-1964
  • 1999  (1,651)
  • Chemistry  (1,469)
  • Life and Medical Sciences  (96)
  • chemotherapy  (86)
  • Nuclear reactions
Source
Material
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  • 1995-1999  (1,651)
  • 1960-1964
Year
Keywords
  • 101
    Electronic Resource
    Electronic Resource
    Alchemie. Lexikon einer hermetischen Wissenschaft. Herausgegeben von Claus Priesner und Karin Figala. Verlag C. H. Beck, München 1998. 412 S., 40 Abb., Leinen, DM 68,-. ISBN 3-406-44104-8 (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 239-240 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330412
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  • 102
    Electronic Resource
    Electronic Resource
    Dokumentation (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 246-246 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330417
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  • 103
    Electronic Resource
    Electronic Resource
    Editorial (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 250-250 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330502
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  • 104
    Electronic Resource
    Electronic Resource
    ChiuZ aktuell (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 308-309 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330508
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  • 105
    Electronic Resource
    Electronic Resource
    Wer und was ist es? (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 312-312 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330511
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  • 106
    Electronic Resource
    Electronic Resource
    Impressum (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 314-314 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330514
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  • 107
    Electronic Resource
    Electronic Resource
    Literaturkarusell. Chemie (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. IX 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330518
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  • 108
    Electronic Resource
    Electronic Resource
    Editorial (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 318-318 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330602
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  • 109
    Electronic Resource
    Electronic Resource
    Chemische Biologie (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 354-358 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Chemical Biology is a rapidly growing field at the interface of organic chemistry and cell biology. Chemical strategies are used to address biological questions not amenable to traditional genetic and biochemical techniques alone. Thc enormous potential of Chemical Biology is illustrated by four recent examples.
    Notes: Chemische Biologie ist eine junge Forschungsrichtung im Grenzgebiet zwischen Organischer Cherme und Zellbiologie, welche aus einem Bedarf nach neuen Techniken zur Untersuchung zellbiologischer Mechanismen entstanden ist. Chemische Methoden werden mit biochemischen und molekularbiologischen Methoden kombiniert, um neuartige Möglichkeiten für die biologische Grundlagenforschung zu schaffen. So werden synthetische Oligosaccharide kovalent an die Oberfläche lebender Zellen gebunden, die Konzentration von Calciumionen im Zytosol künstlich reguliert und Rezeptoren künstlich aktiviert.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330606
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  • 110
    Electronic Resource
    Electronic Resource
    Elektrosynthesen. Strom doppelt genutzt: Erste technische „Paired Electrosynthesis“ (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 373-374 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Eine neue Elektrosynthese erfüllt erstmals den Traum der Elektrochemiker, gleichzeitig Anoden- und Kathodenreaktion für organische Synthesen technisch zu nutzen.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330610
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  • 111
    Electronic Resource
    Electronic Resource
    Experimente für die Chemie (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 377-377 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330614
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  • 112
    Electronic Resource
    Electronic Resource
    Persistenz und Reichweite von Umweltchemikalien. Von M. Scheringer. Wiley-VCh, Weinheim 1999.XIII + 208 Abb.,17Tab., gebunden, DM 158,-.ISBN 3-527-29752-9 (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 380-380 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330618
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  • 113
    Electronic Resource
    Electronic Resource
    Vorbereitungen für die Jahrtausend-Party (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 382-384 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Around the world, BASF has been preparing for Y2K since 1996. The Information services and the Process Control Technology divisions, as well as embedded systems and logistics, not to mention the company's customers and suppliers have all been systenmatically tested for Y2K capability. In addition, special precautionary measures in particular, at large Verbund sites - will be in place during the switchover period.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330621
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  • 114
    Electronic Resource
    Electronic Resource
    Editorial (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 4-4 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330102
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  • 115
    Electronic Resource
    Electronic Resource
    Andere iu Z-Zeitschriften (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 66-66 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330115
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  • 116
    Electronic Resource
    Electronic Resource
    Gentechnik in der Schule (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 104-109 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Fonds of German Chemical Industry (FCI) has produced an instrumental kit named „Blue Genes“ which enables High School teachers to perform in their school environment basic experiments of gene analysis and cloning. In particular, the kit contains all necessary equipment and reagents to perform a restriction analysis, and cloning and expression of a bacterial gene.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330206
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  • 117
    Electronic Resource
    Electronic Resource
    Chemie der Wunder (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 152-157 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: A few physical phenomena believed to be religious miracles are considered, and scientific explanations for them are proposed.
    Notes: Einige physikalische Phänomene, von denen man glaubte, sie seien religiöse Wunder, werden vorgestellt und wissenschaftliche Erklärungen hierfür vorgeschlagen.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330304
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  • 118
    Electronic Resource
    Electronic Resource
    Wer und was ist es? (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 173-173 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330308
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  • 119
    Electronic Resource
    Electronic Resource
    Lebensgeschichten. Sternstunden der frühen Chemie von Johann Rudolph Glauber bis Justus von Liebig. Von Ernst F. Schwenk. Beck'sche Reihe 1252, Verlag C. H. Beck, München 1998. 288 S., 42 s/w-Abb., Paper-back, DM 19,80. ISBN 3-406-42052-4 (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 176-176 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330311
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  • 120
    Electronic Resource
    Electronic Resource
    Literaturkarusell. Interdisziplinäres (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. VIII 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330517
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  • 121
    Electronic Resource
    Electronic Resource
    Literaturkarusell. Pharmazie (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. XIV 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330520
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  • 122
    Electronic Resource
    Electronic Resource
    Kupfer  -  Die biochemische Bedeutung eines Metalls (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 334-341 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The essential trace element copper plays a key role in living systems. Its metalloproteins are involved in various reactions. The IT ononuclear blue copper type-1 proteins take, part in electron transfer processes. Type-2 proteins can either act as oxidases, oxygenases, dioxygenases, or superoxide dismutases, containing one copper core. Dinuclear copper centers of Type-3 proteins are the oxygen transport system hemocyanin, oxidases and oxygenases. Due to this variety of functions copper deficiency and also abundance can cause severe damage of any life form.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330604
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  • 123
    Electronic Resource
    Electronic Resource
    Fritz Haber, Carl Bosch und Friedrich Bergius  -  Protagonisten der Hochdrucksynthese (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 359-364 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is tried to fix the limits between the notions high pressure synthesis and high temperature chemistry. The work of Fritz Haber to apply high pressure to synthetise ammonia and of Friedrich Bergius to liquify coal to synthetise petrol is described. Special attention is given to the merits of Carl Bosch and his coworkers at BASF for applying the high pressure synthesis into industrial scale. The consequences of thc work of Haber, Bergius und Bosch on chemistry, social and political life and their importance for the present are considered.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330607
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  • 124
    Electronic Resource
    Electronic Resource
    Bakterien, Viren, Prionen (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 376-376 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330613
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  • 125
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    Electronic Resource
    Dokumentation (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 390-390 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330622
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  • 126
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    Electronic Resource
    Von Biomineralien zu biomimetischen Materialien: Der Weg ist das Ziel (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 6-19 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Diatoms are unicellular organisms which possess a unique silicified cell wall. Their intricate structures have inspired the imagination of naturalists and scientists throughout centuries. However, molecular biological details about silica metabolic pathways still are obscure. To find out how soft matter can selforganize and create finite solid shapes and complex patterns is certainly one of the most challenging scientific problems today. Especially chemists just have started to unravel the mysteries of chemical morphogenesis.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330103
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  • 127
    Electronic Resource
    Electronic Resource
    ChiuZ aktuell (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 58-60 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330108
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  • 128
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    Electronic Resource
    Chemie im Selbststudium. Grundkurs Chemie I. Allgemeine und Anorganische Chemie. Von Arnold Arni. überarb. Aulf. 3., überarb. Aufl., WILEY-VCH, Weinheim 1998. XIV + 350 S., 66 Abb., 15 Tab., Broschur, DM 54,-. ISBN 3-527-29542-9. Grundkurs Chemie II. Organische Chemie. 2., überarb. Aufl. WILEY-VCH, Weinheim 1998. XIII + 198 S., 16 Abb., 5 Tab., Broschur, DM 48,-. ISBN 3-527-29562-3 (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 60-61 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330110
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  • 129
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    Electronic Resource
    Impressum (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 66-66 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330116
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  • 130
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    Editorial (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 70-70 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330202
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  • 131
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    Wissenschaft aktuell (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 122-125 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330208
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  • 132
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    Dokumentation (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 134-134 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330212
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  • 133
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    Impressum (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 134-134 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330214
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  • 134
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    Electronic Resource
    Literaturkarusell. Chemie (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. X 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330218
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  • 135
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    Editorial (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 138-138 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330302
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  • 136
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    Electronic Resource
    ChiuZ aktuell (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 174-175 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330309
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  • 137
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    Chemie mit Licht. Photochemie. Von D. Wöhrle, M.W. Tausch und W.-D. Stohrer. WILEY-VCH, Weinheim 1998. XVI, 253, S., 169 Abb., 39 Tab., Broschur, DM 128,-.ISBN 3-527-29545-3 (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 175-176 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330310
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  • 138
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    Electronic Resource
    Editorial (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 190-190 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330402
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  • 139
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    Sandwich-artige Cyclopentadienylkomplexe von Hauptgruppenelementen (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 342-353 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cyclopentadienyl (Cp) complexes of maingroup elements are classified and compared in terms of structural types, bonding features, and characteristic reactions. Halfsandwich, sandwich and multidecker sandwich arrangements of different type are observed including cluster species with weak or strong metal-metal bonds. The Cp-El bonding ranges from mainly covalent to purely ionic with important structure-determining intermolecular contacts in the latter. π-Complexation allows the stabilisation of compounds with low-valent elements such as AI(I), Ga(I), and Si(I1). Important reaction principles and applications are shortly described.
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330605
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  • 140
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    Wissenschaft aktuell (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 367-372 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330608
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  • 141
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    ChiuZ aktuell (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 375-375 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330612
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  • 142
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    Schreiben und publizieren in den naturwissenschaften. Vin H.F.Ebel u C. Bliefert. 4., völlig neu bearb. Aufl., WILEY-VCh, Weinheim 1988.XIV + 550 s., Broschur, Dm 68,-ISBN 3-527-29626-3 (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 378-379 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330615
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  • 143
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    Wer war es? (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 381-381 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330620
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  • 144
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    Andere iu Z-Zeitschriften (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 390-390 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330623
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  • 145
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    Wissenschaft aktuell (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 53-58 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330107
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  • 146
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    Koffeinschub für Chemie-Applets im WWW (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 62-63 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330112
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  • 147
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    Wer war es? (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 129-129 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330211
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  • 148
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    Andere iu Z-Zeitschriften (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 134-134 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330213
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  • 149
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    Literaturkarusell. Biologie (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. V 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330216
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  • 150
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    Literaturkarusell. Physik (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. VIII 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330217
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  • 151
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    Impressum (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 186-186 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330315
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  • 152
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    Methyltrioxorhenium (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 192-198 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330403
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  • 153
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    Molekulare Aspekte des Alterns (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 221-225 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the last decade, major advances in the understanding of the biology of aging were made. Studies in worms, flies and yeast led to the identification of several life-extending genes. In mammals, two genes were found which, when mutated, shorten life span. Previous studies in rodents reporting life span prolongation by caloric restriction were confirmed and extended to lower organisms. The studies arc consistent with and supportive of the free radical theory of aging, which secs reactive oxygen species as the main contributor to aging. A refinement of this theory puts mitochondrial DNA into the center of the aging process. It appears that mitochondrial DNA may be both, a yardstick for the biological age and a signalling device to tell the organism when to die. A diet low in calories and high in antioxidants promises to lead to a better quality of life at old age and possibly to increased life span for humans.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330407
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  • 154
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    ChiuZ aktuell (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 237-239 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330411
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  • 155
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    Radikale und Radikalionen in der Organischen Synthese. Von Torsten Linker und Michael Schmittel. WILEY-VCH, Weinheim 1998. 421 S., DM 88,-. ISBN 3-527-29492-9 (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 241-241 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330415
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  • 156
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    Impressum (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 247-247 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330419
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  • 157
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    Wiederaufladbare Batterien (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 252-266 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This first part of „Rechargeable Batteries“ is devoted to materials and reactions in batteries with aqueous electrolytes. Lead-acid, nickelcadmium, nickel-metal hydride, and various zinc systems, such as zinc-manganese oxide, zinc-air, and zinc-bromine cells are discussed. Special attention is paid to the limited electrochemical stability window of the aqueous electrolytes, which enables overcharge and overdischarge protection of the battery but limits cell voltages to less than 2 Volts. In the following part of this article we will focus on nonaqueous electrolyte-based rechargeable batteries. Due to thc wider electrochemical stability window of these electrolytes high specific charge and high cell voltage batteries can be realized, e.g., the „4 V“ lithium ion cell.
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330503
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  • 158
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    Wissenschaft aktuell (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 304-308 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330507
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  • 159
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    Dokumentation (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 314-314 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330512
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  • 160
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    Chemie erlebt - 50 jahre GDCH. Hrsg. von der Gesellschaft Deutscher Chemiker. Das Buch ist im Eigenverlag erschienen und kann bei der Gesellschaft Deutscher Chemiker, Abteilung Öffentlichkeitsarbeit, Postfach 900440,60444 Frankfurt/M bestellt werde,304 S., Dm 39,-ISBN 3-924763-79-8 (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 379-380 
    Details
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330616
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  • 161
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    Impressum (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 390-390 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330624
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  • 162
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    Feste Lösungen (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 33-44 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Solid solutions arc an area of inorganic chemistry that encompasses a wide variety of natural and synthetic compounds. This article is intended to be a selection of interesting examples which illustrate the importance of solid solutions in everyday life and industrial applications. A short discussion of the theoretical background is given, followed by the description of solid solutions of non-metals in metals such as steel. Furthermore, solid solutions with important optical (e.g. laser materials) and electrical properties (e.g. β-alumina) are discussed, referring to their chemical structure and technological relevance.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330105
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  • 163
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    ChiuZ aktuell (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 126-127 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330209
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  • 164
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    Primärprozesse der Photosynthese und ihre Modellierung (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. 72-83 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photosynthesis is one of the most fascinating fields of current interdisciplinary research. It seems miraculous that Nature, in the process of evolution, has managed to bring about a 100% quantum yield in charge separation occurring in the primary processes within the photosynthetic reaction centers. In fact, wasteful deactivation of the photoexcited electronic states into the ground state should be favoured and thus prevent charge separation. Biomimetic model compounds have been synthesized, essentially from porphyrins and quinones, resembling the redoxactive cofactors, Nature has developed. The underlying philosophy of this approach is to design and prepare suitable organic molecules allowing the specific properties of the complex electron transfer reactions to be tuned appropriately. Special emphasis is given the through comparison of structures and functions of native and artificial systems. The prominent electron transfer characteristics are discussed in particular by using time-resolved picosecond fluorescence and time-resolved EPR techniques.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330203
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  • 165
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    Literaturkarusell. Pharmazie (1999)
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 33 (1999), S. XI 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330219
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  • 166
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    Literaturkarusell. Inter-disziplinäres (1999)
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    Chemie in unserer Zeit 33 (1999), S. XIII 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330220
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  • 167
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    Biochemische Mechanismen einer einfachen Verhaltensreaktion (1999)
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    Chemie in unserer Zeit 33 (1999), S. 140-151 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In active search for conditions for optimal phototrophic growth, halobacteria respond to light and to a variety of other environmental stimuli by taxis. Light reception is mediated by sensory rhodopsins, seven helix transmembrane retinal proteins that are stably complexed to specific MCP-related transducer proteins. Photoisomerization of the retinal chromophore generates a steric signal which activates the sensory rhodopsin-transducer-complex. Complex activation is relayed to a two component signaling system and transiently changes the cytoplasmic concentration of fumarate which, together with the small cytoplasmic protein CheY controls flagellar motor switching. Dual signaling by CheY and fumarate was also found in Escherichia coli where it mediates metabolic signaling and taxis in cells with disabled two-component system. Sensory integration of different environmental stimuli occurs at the level of the signaling domains of several stimulus-specific transducers constructed through combination of appropriate molecular modules. Irrespective of the complexity of the signaling network, the response to light is quantitatively predictable and stochastic. Its kinetic analysis suggests that time-dependent changes in the activity of signaling components can be resolved even in the context of a complex molecular network.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330303
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    Wissenschaft aktuell (1999)
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    Chemie in unserer Zeit 33 (1999), S. 167-172 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330307
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  • 169
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    Dokumentation (1999)
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    Chemie in unserer Zeit 33 (1999), S. 186-186 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330313
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  • 170
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    Rückblick (1999)
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    Chemie in unserer Zeit 33 (1999), S. 187-187 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330316
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  • 171
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    Wissenschaft aktuell (1999)
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    Chemie in unserer Zeit 33 (1999), S. 228-233 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330408
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    Wiederaufladbare Batterien (1999)
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    Chemie in unserer Zeit 33 (1999), S. 320-332 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: As a matter of fact, most of our technical electrochemical energy storage systems operate outside the limitations of thermodynamics. As in the case of rechargeable batteries with aqueous electrolytes (part I of this article), kinetics control the operation and safety also in batteries with nonaqueous electrolytes (this second and final part).A striking example is the lithium ion battery which possesses an operating voltage of 〉3,5 V and a very high energy density. From a thermodynamic viewpoint such a cell is impossible because the used organic electrolyte is in contact with two lithium insertion electrodes that operate at extreme reducing and oxidizing potentials, respectively. However, a unique mechanism kinetically prevents the decomposition of the electrolyte due to the formation of electronically insulating interphases between electrode and electrolyte that are still permeable to the electrochemically active Li+ cations. Lithium ion batteries have already made their breakthrough into the market as small format systems for portable electronics. The only „kinetically shielded“ high energy density, however, might be a safety complication for large format batteries, which are assembled for electric vehicle (EV) propulsion. Safety concerns are also valid for high temperature (300°C) batteries such as the sodium-sulfur and sodium-nickel chloride systems. These systems are still in the stage of „experimental batteries“, which may find future application in large units for EV's or uninterruptible power systems. The paper is concluded by a performance comparison of various rechargeable battery systems with aqueous and nonaqueous electrolytes. (Possible) applications in consumer electronics and EV's are discussed in more detail.
    Additional Material: 13 Ill.
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    URL: http://dx.doi.org/10.1002/ciuz.19990330603
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    Pflanzeninhaltsstoffe. Chemische Abschreckung von Fraßinsekten (1999)
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    Chemie in unserer Zeit 33 (1999), S. 372-372 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330609
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    Rückblick (1999)
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    Chemie in unserer Zeit 33 (1999), S. 391-391 
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    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ciuz.19990330625
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  • 175
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    Epidermal Growth Factor Receptor Inhibition in Cancer Therapy: Biology, Rationale and Preliminary Clinical Results (1999)
    Springer
    Investigational new drugs 17 (1999), S. 259-269 
    Details
    ISSN: 1573-0646
    Keywords: EGFR ; cancer ; anti-EGFR antibody ; chemotherapy ; radiation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Abstract The epidermal growth factor receptor (EGFR), a growth factor receptor involved in the regulation of cellular differentiation and proliferation, is highly expressed by many tumor cells. In light of a relationship between overexpression of EGFR and clinically aggressive malignant disease, EGFR has emerged as a promising target for cancer therapy. In recent years, several molecular strategies have been explored to modulate either the EGFR itself, or the downstream signal beyond the cell surface receptor. One of the most promising current strategies involves the use of anti-EGFR monoclonal antibodies (mAbs), either alone or in combination with conventional cytotoxic modalities such as chemotherapy or radiotherapy. This review focuses primarily on recent progress in the development of anti-EGFR mAbs, and examines their potential in the treatment of cancer.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1006384521198
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  • 176
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    Oral Mucosal Permeability and Stability of Transforming Growth Factor Beta-3 In Vitro (1999)
    Springer
    Pharmaceutical research 16 (1999), S. 1557-1563 
    Details
    ISSN: 1573-904X
    Keywords: transforming growth factor ; permeability ; chemotherapy ; oral mucosa ; mucositis and pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. To investigate the permeability and localization of topically applied 125I-TGF-β3 in porcine floor-of-mouth mucosa as a function of concentration and exposure. Methods. The 125I-TGF-β3 diluted in three different vehicles was applied to the tissue samples mounted in perfusion cells maintained at 37°C. Flux and Kp values were calculated from the perfusate collected over a 24 hour period. The quantity of 125I-TGF-β3 present in the tissue was determined by horizontal sectioning and subsequent counting. The stability of 125I-TGF-β3 in saliva and in the tissue was analyzed by SDS polyacrylamide gradient gel electrophoresis. Results. 125I-TGF-β3 was relatively stable in saliva and in the epithelium; approximately 50% of the total counts in the deeper epithelium were resident in the 25kDa TGF-β3 homodimer. A steady-state flux was reached ∼6 hours post application and Kp value was 4.0 ± 0.6 × 10-6 (mean ± sem). Penetration of 125I-TGF-β3 to the basal cell layer was concentration dependent but reached nanomolar concentrations even after extensive surface rinsing, representing over one-thousand fold the IC50 for epithelial cell cycle arrest. Conclusions. The data suggest that topical application of TGF-β3 to the oral mucosa in an appropriate vehicle can provide effective therapeutic delivery to the tissue.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1015052520467
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  • 177
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    Photochemistry of 9,10-Dicarbonyl-9,10-dihydroanthracene - A Source of 9,10-Dehydroanthracene? (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 57-60 
    Details
    ISSN: 1434-193X
    Keywords: Benzyne ; Dehydroanthracene ; Matrix isolation ; Photochemistry ; Bergman reaction ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -9,10-Didehydroanthracene (1) is an interesting derivative of p-benzyne that has been subject of several studies. In contrast to an earlier report, the photochemical decarbonylation of 9,10-dicarbonyl-9,10-dihydroanthracene (2) does not lead to 1 but rather to the ring-opened ene-diyne 4. The key intermediate for this reaction is keto carbene 7 which is formed by monodecarbonylation of 2. Carbene 7 is labile towards visible-light irradiation and easily looses the second CO molecule to give 4. Carbene 7 and diyne 4 are characterized by IR and UV/Vis spectra, the IR spectra are compared to calculations at the B3LYP/6-31G(d,p) level of theory.
    Additional Material: 2 Ill.
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  • 178
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    Reversal Diastereofacial Selectivity in the n-Butyllithium Addition to O-Protected N-Trimethylsilylimines of (2S)-Lactal: Enthalpic versus Entropic Contributions (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 61-65 
    Details
    ISSN: 1434-193X
    Keywords: Nucleophilic addition ; Solvent effect ; Reversal of diastereoselectivity ; Temperature effect ; Imines ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Commonly observed, but rarely explored, is the possibility of modifying the diastereomeric excess (de%) by means of temperature. A complete reversal in the diastereofacial selectivity could be obtained whenever the diastereoisomers concerned are differentially favored by enthalpy and entropy. The enthalpic or entropic dominance of a diastereoisomer depends greatly on the reaction solvent used.
    Additional Material: 1 Ill.
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  • 179
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    Syntheses of Donor-Acceptor-Substituted 2,6-Stellanes (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 73-81 
    Details
    ISSN: 1434-193X
    Keywords: Donor-acceptor systems ; Cage compounds ; Stelladione ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -A number of condensations could be carried out using tricyclo[3.3.0.03,7]octane-2-one (stellanone, 4) and tricyclo[3.3.0.03,7]octane-2,6-dione (2,6-stelladione, 5) as starting materials. The components for condensations were 2-trimethylsilyl-1,3-dithiane (6), 1,1-bis(trimethylsilyl)-1H-cyclopropa[b]naphthalene (7), its 3,6-dimethoxy-substituted analogue 8, fluorene (12), xanthene (13), diethyl malonate (14), and malononitrile (15). The condensation reactions with 5 yielded mono- and disubstituted products, among them were the donor-acceptor-substituted 2,6-stellanes 33-35. The structures of 18 (prepared from stellanone and fluorene), 19, 24, 27, 31 and 32 (synthesized by condensation of 2,6-stelladione and 2-trimethylsilyl-1,3-dithiane and malononitrile, respectively) were determined by X-ray crystallography.
    Additional Material: 1 Ill.
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  • 180
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    Synthesis of ω-Nitro Acids and ω-Amino Acids by Ring Cleavage of α-Nitrocycloalkanones (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 87-90 
    Details
    ISSN: 1434-193X
    Keywords: Water ; α-Nitrocycloalkanones ; ω-Nitro acids ; Surfactant ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -The reaction of various α-nitrocycloalkanones 1 with aqueous 0.05 M NaOH, at 80 °C, in the presence of cetyltrimethylammonium chloride (CTACl) as a cationic surfactant, produces ω-nitro acids 2 in good yields. Reduction of the latter with HCOONH4/Pd-C, in methanol, at 80 °C affords ω-amino acids 3. The synthesis of methyl 9-oxodecanoate (8) is also reported.
    Additional Material: 2 Tab.
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  • 181
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    On the Selective O-Alkylation of Ambident Nucleophiles - The Synthesis of Thiohydroxamic Acid O-Esters by Phase-Transfer Reactions (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 97-106 
    Details
    ISSN: 1434-193X
    Keywords: O-Alkylation ; Ambident nucleophile ; Thiazolethione ; Thiohydroxamic acid ; Phase-transfer reaction ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -O-Alkylation of cyclic thiohydroxamic acids 1 and 3-5 has been studied with a view to developing an efficient method for the synthesis of N-(alkoxy)pyridine-2(1H)-thiones and N-(alkoxy)thiazole-2(3H)-thiones. Four issues have been addressed and the following conclusions can be drawn: (i) Thiones 1 and 5 exist as O-H acids in the solid state. (ii) According to NMR investigations (1H, 13C), the thione structures should be largely retained in CDCl3, [D6]DMSO, and CD3OD solutions of acids 1, 3-5, as is also the case for pyridinethione salts 2a-h. (iii) O-Alkylation of pyridinethione salts occurs in competition with S-alkylation. Selective O-alkylation is however possible, if thiohydroxamate salts with large countercations, such as M = NBu4, are treated with hard alkylating reagents in polar aprotic media. (iv) As tetrabutylammonium thiohydroxamates, such as 2f, are highly useful in the synthesis of cyclic thiohydroxamic acid O-esters, we have developed an efficient protocol for the preparation of N-(alkoxy)pyridine-2(1H)-thiones directly from acid 1 using phase-transfer conditions (alkyl halide or sulfonic acid ester, CH3CN, K2CO3, Bu4NHSO4). This method has proved particularly successful for the synthesis of N-(alkoxy)thiazole-2(3H)-thiones 11, 20-28, which were obtained in yields of up to 87%.
    Additional Material: 2 Ill.
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  • 182
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    Palladium(0)-Catalyzed Asymmetric Synthesis of 1,2,3,4-Tetrahydro-2-vinylquinoxalines (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 129-134 
    Details
    ISSN: 1434-193X
    Keywords: Tetrahydro-2-vinylquinoxaline ; Cyclization ; Palladium ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Reaction of (Z)-1,2-bis(methoxycarbonyloxy)but-2-ene (2) with various N,N-bis(arylsulfonyl)-o-phenylenediamines 1 was catalyzed by a palladium complex associated with chiral ligands to give optically active 1,4-bis(arylsulfonyl)-1,2,3,4-tetrahydro-2-vinylquinoxalines 3 with up to 62% ee. The use of (S)-MeOBIPHEP as the chiral ligand and N,N-bis(p-tolylsulfonyl)-o-phenylenediamine (1i) as the nucleophile led to the highest ee at 25 °C, regardless of the solvent used. The enantioselectivity of the cyclization is strongly affected by the nature of the substituents at the nitrogen atom.
    Additional Material: 4 Tab.
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  • 183
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    Stereoselective Synthesis of Enantiomerically Pure β-Fluoroalkyl γ-Butyrolactones by Sulfoxide-Directed Lactonization (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 111-115 
    Details
    ISSN: 1434-193X
    Keywords: Fluorine ; Lactones ; Annulation ; Ketene ; Sulfoxides ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Enantiomerically pure α,α-dichloro β-fluoroalkyl γ-p-tolylthio γ-butyrolactones trans-6a-c have been obtained with excellent stereocontrol (〉 98:2) and enantiomeric purity (〉 98:2) by sulfoxide-directed lactonization (Marino's annu-lation reaction) of β-fluoroalkyl vinyl sulfoxides (R)-(E)-5a-c with dichloroketene. Highly chemoselective dechlorination and desulfurization reactions performed on trans-6c efficiently provided the β-chlorodifluoromethyl γ-butyrolactone (S)-8c, the absolute stereochemistry of which was determined by X-ray diffraction analysis of its γ-p-tolylthio precursor (2R,3S)-7c.
    Additional Material: 1 Ill.
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  • 184
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    Reaction of Nitrosobenzene with 4-Methoxy-N-methyleneaniline (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 141-143 
    Details
    ISSN: 1434-193X
    Keywords: Nitrosobenzene ; 4-Methoxy-N-methyleneaniline ; 1,3,5-Tris(4-methoxyphenyl)-1,3,5-triazinane ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -A 1:1 adduct produced in the reaction of nitrosobenzene (2) with 1,3,5-tris(4-methoxyphenyl)-1,3,5-triazinane (3) has been shown by X-ray diffraction structure analysis to be the N′-(4-methoxyphenyl)-N-phenyl-N-oxyformamidinium species 5.
    Additional Material: 1 Ill.
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  • 185
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    A New Diastereoselective Synthesis of anti-α-Alkyl α-Hydroxy β-Amino Acids (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 155-161 
    Details
    ISSN: 1434-193X
    Keywords: Alkylation ; Oxazolines ; anti-α-Alkyl α-hydroxy β-amino acids ; Lithium dianion ; Penicillin G acylase ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -As part of an ongoing project concerning the synthesis of enantiomerically pure α-hydroxy β-amino acids, we have now developed a general strategy allowing the synthesis of anti-α-alkyl α-hydroxy β-amino acids. Our procedure involves the intermediate formation of trans-oxazolines, which are alkylated at C-5 with good to high diastereoselectivity and then hydrolysed under mildly acidic conditions, affording in quantitative yield the corresponding hydroxy amides. The starting (R)-3-amino-3-phenylpropanoic acid and (S)-3-aminobutanoic acid were obtained in enantiomerically pure form by selective enzymatic hydrolysis of the corresponding phenylacetylamides with penicillin G acylase.
    Additional Material: 3 Ill.
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  • 186
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    Palladium(0)-Catalyzed Reaction of Acidic Anilines with (Z)-2-Butene-1,4-diyl Dicarbonate - Preparation of N-Aryl-4-vinyloxazolidin-2-ones (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 181-186 
    Details
    ISSN: 1434-193X
    Keywords: Palladium catalysis ; Homogeneous catalysis ; Anilines ; Alkylation ; Oxazolidinones ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Palladium-catalyzed reaction of acidic anilines with (Z)-2-butene-1,4-diyl dicarbonate affords N-aryl-4-vinyloxazolidin-2-ones. The success of the reaction depends on the acidity of the aniline and requires in situ conversion of the dicarbonate into carbamate carbonate by nucleophilic attack of the aniline conjugate base followed by palladium-catalyzed intramolecular cyclization.
    Additional Material: 1 Tab.
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  • 187
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    Substituent Effects on the Vinylcyclopropane-Cyclopentene Rearrangement - A Theoretical Study by Restricted and Unrestricted Density Functional Theory (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 215-220 
    Details
    ISSN: 1434-193X
    Keywords: Density functional calculations ; Vinylcyclopropane-cyclopentene rearrangement ; [1,3]-Sigmatropic shift ; Biradical-like transition structure ; Substituent effects ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -The effect of donor substitution by the hydroxy group and of acceptor substitution by the cyano group on the activation energies of the vinylcyclopropane-cyclopentene rearrangement was calculated by the spin-restricted RB3LYP/6-31G* method for reactant structures and by the spin-unrestricted UB3LYP/6-31G* method for transition structures. The activation energies of the rearrangement of hydroxy- and cyano-substituted vinylcyclopropanes are very similar for substitution in the same position. In agreement with earlier findings the substituent effects on the activation energies are closely connected with the radical stabilizing properties of the substituents. As indicated by singlet/triplet splitting energies, the transition structures are essentially biradicaloid. In spite of spin pairing in the transition structure the substituent effects on bond lengths and on stabilization energies are very similar to those of the free radicals corresponding to the two radical substructures. Thus, the transition structures may be considered, in good approximation, as structures consisting of two weakly interacting radicals.Supporting information for this article is available on the WWW under -http://www.wileY-Vch.de/contents/jc_2046/1999/98349_s.pdf or from the author.
    Additional Material: 5 Ill.
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  • 188
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    Syntheses and Reactions of 1-Amino-2,2-dialkylcyclopropane-1-carbonitriles and -carboxamides - Potential Precursors of ACC Derivatives (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 239-250 
    Details
    ISSN: 1434-193X
    Keywords: Cyclopropanes ; Rearrangements ; Cyanohydrins ; Schiff bases ; Small ring systems ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -The direct cyclization of 2-amino-4-chloro-3,3-dimethylbutanenitrile with potassium tert-butoxide in THF afforded 1-amino-2,2-dimethylcyclopropane-1-carbonitrile and a dimerization product. Various new cis- and trans-1-(tert-butylamino)-2-benzyl-2-methylcyclopropane-carbonitriles and© the corresponding cyclopropanecarboxamides have been synthesized, with focus on the isolation of the pure stereoisomeric cyclopropanecarboxamides. The relative configuration of the stereoisomers was established by X-ray crystallographic analysis of one of the model compounds. A new route to the latter functionalized cyclopropanes was developed by reaction of 1-methoxycyclopropylamines with potassium cyanide. Some remarkable rearrangements of 1-aminocyclopropane-1-carbonitriles into azetidine and oxazine derivatives via Favorskii-derived intermediates are reported. Various aspects of the chemistry of geminally functionalized cyclopropanes are discussed.
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  • 189
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    Regio- and Stereoselective Synthesis of Vinylallenes by 1,5-(SN′′)-Substitution of Enyne Acetates and Oxiranes with Organocuprates (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 267-275 
    Details
    ISSN: 1434-193X
    Keywords: Vinylallenes ; Organocuprates ; Substitution ; Stereoselective synthesis ; Copper catalysis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Enyne acetates 2, 4, 6, and 8, as well as enyne oxiranes 10, with different substitution patterns react with organocuprates regioselectively under 1,5-(SN2′′)-substitution to provide vinylallenes 11 and 12. With lithium dimethylcuprate, reduced vinylallenes originating from a (formal) transfer of a hydride ion to the substrate are formed in some cases. The products are usually obtained as mixtures of (E/Z)isomers; however, pure (E)-vinylallenes are formed occasionally. The 1,5-substitutions can also be carried out with catalytic amounts of copper reagents. The reaction of chiral enyne acetate (S)-2a with tBu2CuLi · LiCN proceeds enantioselectively, so that this transformation constitutes a new case of remote stereocontrol.
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  • 190
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    Reactions of the Hydrofluoroborate Salts of Open-Chain Analogues of Reissert Compounds with Some α,β-Ethylenic Esters (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 297-303 
    Details
    ISSN: 1434-193X
    Keywords: Nitrogen heterocycles ; Open-chain analogue of Reissert compound ; Hydrofluoroborate salts ; α,β-Ethylenic esters ; 1,3-Dipolar cycloaddition ; Azomethine ylide ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -The reaction of the hydrofluoroborate salt of an open-chain analogue of a Reissert compound with some α,β-ethylenic esters does not give a [4 + 2] cycloadduct, as previously described in the case of ethyl acrylate. The reaction starts with a 1,3-dipolar cycloaddition of a münchnone imine 5c, d. The [3 + 2] cycloadducts 13 evolve via a rearrangement-condensation sequence to give a substituted 2-pyridone derivative 18 or 19. The proposed mechanism has been verified by the isolation and structural X-ray analysis of some compounds of the reaction sequence.
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  • 191
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    EPC-Synthesis of β-Amino Acid Derivatives through Lithiated Hydropyrimidines (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 335-360 
    Details
    ISSN: 1434-193X
    Keywords: 2-tert-Butylhydropyrimidinones ; 3-Aminocarboxylic acid derivatives ; Cyclic imino esters ; Lithium enaminates ; Alkylations ; β-Amino acids ; Asymmetric synthesis ; Kinetic resolution ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Racemic and enantiopure 2-tert-butyltetrahydropyrimidinones (from pivalaldehyde and 3-aminocarboxylic acids) are converted to Alloc-, Boc-, and Z-protected cyclic imino esters (7-10, Schemes 2-4). These are deprotonated to Li enaminates (K, L). Reactions with electrophiles (prim., sec. alkyl, allyl, benzyl, propargyl halides, aldehydes, imines, enoates) give good yields and are highly diastereoselective (products 11-42, Schemes 5-10). A two-step cleavage (removal of protecting group and hydrolysis) under very mild conditions converts the heterocyclic products to α-branched β-amino acid methyl esters (43-61, Schemes 11-13). The structure of the products is determined by NMR spectroscopy (Figure 1), by chemical correlation (Scheme 14), and by X-ray analysis (Figure 2, 3, 7, Table 1). A structure of the Li enaminates is proposed (Figure 4). Mechanistic models are derived for the reactions occurring with formation of two stereogenic centers with relative topicity like (Figures 5, 6).
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  • 192
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    A Unified Synthetic Strategy for the Indolopyridine Alkaloid Group (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 373-378 
    Details
    ISSN: 1434-193X
    Keywords: Alkaloids ; Cross-coupling ; N-Heterocycles ; Palladium ; Synthesis design ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Thermal or acetyl chloride induced cyclization of bromoenamide 10 affords the pentacyclic derivative 12 with high yield and regioselectivity. From this common synthetic intermediate, palladium-catalyzed reactions allow the total synthesis of indolopyridine alkaloids 1-6.Supporting information for this article is available on the WWW under -http://www.wileY-Vch.de/contents/jc_2046/1999/98332_s.pdf or from the author.
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  • 193
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    Conformational Preferences of Peptides Containing Reverse-Turn Mimetic Bicyclic Lactams: Inverse γ-Turns versus Type-II′ β-Turns - Insights into β-Hairpin Stability (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 389-400 
    Details
    ISSN: 1434-193X
    Keywords: Reverse-turn mimics ; γ-Turns ; β-Turns ; β-Hairpins ; NMR spectroscopy ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -The solid-phase synthesis and characterization of a series of peptides (3-9), containing reverse-turn mimetic bicyclic lactams (1a, 1b), was reported in the preceding paper. The bicyclic lactams (1a, 1b) possess high structural similarity to the two central residues of a β-turn. The conformational preferences of the constrained peptides have been investigated by NMR spectroscopy and IR spectroscopy. Our experimental results have been complemented by computer modelling studies and show that the constrained peptides (3-9) form an inverse γ-turn or a type-II′ β-turn through intramolecular hydrogen bonding, depending on the nature of the reverse-turn mimic. In N-acetylated tetrapeptide mimics incorporating the two different bicyclic lactams (a series and b series), H5 is available for either a γ-turn (7-membered ring with the carbonyl group of the bicyclic lactam) or a β-turn (10-membered ring with the carbonyl group of residue 2), as shown in Figures 7 and 9. The a series incorporating the (5,7)-bicyclic lactam predominantly induces the γ-turn conformation, while the b series incorporating the (5,6)-bicyclic lactam can promote either a γ-turn or a β-turn conformation, with the β-turn usually being preferred and with varying degrees of β-hairpin formation.
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  • 194
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    Deprotonation of Oxazolinyloxiranes: Formation of Substituted Acyloxiranes (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 409-417 
    Details
    ISSN: 1434-193X
    Keywords: Deprotonation ; Oxiranyloxazolines ; Oxazolinyloxiranyllithium compounds ; Oxazolidines ; Acyloxiranes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Deprotonation of oxazolinyloxiranes 1a, 1h, and 1k with sBuLi/TMEDA at -100 °C in Et2O furnishes oxazolinyloxiranyllithium compounds[1]1b, 1i, and 1l which are stable at low temperature and can be trapped with electrophiles to give substituted oxiranes 1c-1g and 1j. The reaction of 1b with aldehydes produced diastereomers syn (2a-d) and anti (3a-d). Oxiranyllithium 1i from trans-1-(4,4-dimethyl-2-oxazolinyl)-2-p-tolylepoxyethane (1h) was found to be configurationally stable while oxiranyllithium 1l, generated from the cis isomer 1k, was not. Oxazolinylepoxides 1d, 1j, and 1m could be deblocked to acyloxiranes 5a-e through oxazolidines 4a-e.
    Additional Material: 2 Ill.
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  • 195
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    N-Substituted 1-Aminoindoles from Electrogenerated N-Substituted 2-(ortho-Nitrosophenyl)ethylamines (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 419-430 
    Details
    ISSN: 1434-193X
    Keywords: Electrochemistry ; Electrosynthesis ; Nitrosobenzenes ; Nitrogen heterocycles ; 1-Aminoindoles ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -An electrochemical methodology offering efficient access to N-alkyl- and N-aryl-substituted 1-aminoindoles has been developed. N-Substituted 2-(ortho-nitrosophenyl)ethylamines, electrogenerated in a “redox” flow cell, undergo intramolecular cyclization to hydrocinnoline-type intermediates. Under slightly basic conditions, these undergo spontaneous ring-contraction to produce the N-substituted heterocycles in good yields. The reactions have been studied in slightly acidic and slightly basic aqueous alcoholic media.
    Additional Material: 11 Ill.
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  • 196
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    Synthesis of Enantiopure β- and γ-Amino Alcohols from Homochiral α- and β-Aminoacylsilanes as Stable Synthetic Equivalents of α- and β-Amino Aldehydes (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 437-445 
    Details
    ISSN: 1434-193X
    Keywords: Aminoacylsilanes ; Amino aldehydes ; Amino alcohols ; Allylation ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -A practical route is described for the synthesis of enantiopure β- and γ-amino alcohols with two stereocenters, starting from homochiral α- (1 and 5) and β- (13 and 16) -aminoacylsilanes, and involving stereoselective addition of allylmetal compounds and subsequent stereospecific protiodesilylation of the adducts. The degree of diastereoselectivity achieved in the nucleophilic addition step depends on both the nitrogen-protecting group and the reagents used. Diastereomeric excess (de) values equal to or higher than 98% were obtained in the TiCl4-promoted allylation of the N-Pht-aminoacylsilanes 1 and 13 and of the N-Ts-aminoacylsilane 5 with allyltrimethylsilane. Lower de values were obtained in the Sc(OTf)3-catalyzed allylation of 5 with tetraallyltin and in the additions of both allyltrimethylsilane and tetraallyltin to the N-Ts-β-aminoacylsilane 16. Protiodesilylation of the adducts, leading to the β- and γ-amino alcohols, was accomplished with TBAF, except in the case of the adducts obtained from 5. For these, a preliminary removal of the tosyl group was necessary, which was accomplished with simultaneous desilylation by treatment with Na in liquid ammonia.Supporting information for this article is available on the WWW under -http://www.wileY-Vch.de/contents/jc_2046/1999/98342_s.pdf or from the author.
    Additional Material: 1 Tab.
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  • 197
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    Diastereoselective Intramolecular meta Photocycloaddition of Side-Chain-Substituted 5-(2-Methoxyphenyl)pent-1-enes (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 463-470 
    Details
    ISSN: 1434-193X
    Keywords: meta Photocycloaddition ; Photochemistry ; Steric hindrance ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Irradiation of a series of 5-(2-methoxyphenyl)pent-1-enes substituted with a hydroxy or trimethylsilyloxy group at the α-, β-, or γ-position of the side-chain yields in all cases meta photocycloadducts, in which the configuration at the substituted carbon atom is mainly endo. This indicates that the diastereoselectivity originates from minimization of steric interactions between the side-chain substituent and the ortho-methoxy group at the arene unit. Hydrogen bonding does not seem to be involved. The introduction of the side-chain substituents also influences the regioselectivity of the addition: The linear to angular adduct ratios are significantly increased compared to the case of the parent compound.
    Additional Material: 3 Tab.
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  • 198
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    5-Aza-7-deaza-2′-deoxyguanosine: Oligonucleotide Duplexes with Novel Base Pairs, Parallel Chain Orientation and Protonation Sites in the Core of a Double Helix (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 485-496 
    Details
    ISSN: 1434-193X
    Keywords: 5-Aza-7-deaza-2′-deoxyguanosine ; Oligonucleotides ; Parallel DNA ; Protonated base pairs ; Tm values ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Oligonucleotides containing 5-aza-7-deaza-2′-deoxyguanosine (1) were synthesized. Solid-phase synthesis was performed with the phosphonate 15 or the phosphoramidite 5. The amino-unprotected phosphonate 4 was also employed. Hybridization studies of oligonucleotides containing 1 resulted in new base pairs leading to duplexes with parallel (ps) or antiparallel (aps) chain orientation. Among those with parallel chains a stable “purine-purine” base pair was observed between 5-aza-7-deazaguanine and guanine or 7-deazaguanine. Antiparallel stranded duplexes are formed when 5-aza-7-deazaguanine pairs with cytosine. This base pair has only two hydrogen bonds under neutral conditions but is stabilized by a third one in acidic medium. A new base pair is also detected between the base of 1 and isoguanine (neutral medium).
    Additional Material: 1 Ill.
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  • 199
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    Polar and Steric Substituent Effects in 5-exo-trig Cyclizations of 1-Aryl-4-penten-1-oxyl Radicals (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 523-523 
    Details
    ISSN: 1434-193X
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -By mistake wrong concentrations were given in the footnote of Table 1 and in the Discussion. Instead of c0 = 1.2 M read c0 = 0.12 M if 2-naphthalenethiol was used as hydrogen donor and instead of c0 = 1.8 M read c0 = 0.18 M if Bu3SnH was used to trap photoproducts. In Table 2 relative rate constants of radical 2d refer to radical 2e and vice versa as correctly stated in the Discussion. In the Experimental Section (Iodocyclization) read 2.25 g (8.86 mmol) of iodine instead of 2.25 g (1.10 mmol) of iodine.
    Type of Medium: Electronic Resource
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  • 200
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    Arylboron Compounds as Acid Catalysts in Organic Synthetic Transformations (1999)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 527-538 
    Details
    ISSN: 1434-193X
    Keywords: Tris(pentafluorophenyl)borane ; Diarylborinic acid ; Arylboronic acid ; Chiral arylboron catalyst ; Lewis acid ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: -Arylboron compounds, ArnB(OH)3-n (n = 1-3), bearing electron-withdrawing aromatic groups such as triarylboranes, diarylborinic acids, and arylboronic acids represent a new class of air-stable and water-tolerant Lewis acid or Brønsted acid catalysts in organic synthesis. In particular, while tris(pentafluorophenyl)borane has primarily been used as a co-catalyst in metallocene-mediated olefin polymerization, its potential as a Lewis acid catalyst for organic transformation is now much more extensive. Diarylborinic acids and arylboronic acids have shown themselves to be powerful tools in the design of chiral boron catalysts. This article provides a comprehensive summary of the organic transformations catalyzed by arylboron compounds as acids.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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