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  • 1
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of (η2-Ethene)bis(triphenylphosphane)platinum(0) with Dimeric Hexafluorothioacetone. Preparation and Structure of Platina Cyclopentane and Cyclopropane DerivativesThe five-membered (CS)2Pt ring 1 was obtained by the reaction of 2, 2, 4, 4-tetrakis(trifluoromethyl)-1,3-dithietane and (η2-ethene)bis(triphenylphosphane)platinum(0) at low temperatures. 1 is converted at its melting point to the three-membered CSPt ring derivative 2, with elimination of one molecule of hexafluorothioacetone. 2 is also formed directly when the reaction is conducted at temperatures above +30°C. 2 was characterized by an X-ray Structural analysis.
    Notes: Der fünfgliedrige (CS)2Pt-Cyclus 1 kann aus 2, 2, 4, 4-Tetrakis(trifluormethyl)-1,3-dithietan und (η2-Ethen)bis(triphenylphosphan)-platin(0) bei tiefer Temperatur erhalten werden. 1 wandelt sich an seinem Schmelzpunkt unter Abspaltung eines Moleküls Hexafluorthioaceton in den um zwei Ringglieder reduzierten CSPt-Ring 2 um, der auch auf direktem Wege durch Umsetzen des Dithietans bei Temperaturen oberhalb von +30° zugänglich ist. 2 konnte erstmals durch eine Kristallstrukturbestimmung charakterisiert werden.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reaction of Metal and Metalloid Compounds with Polyfunctional Molecules. XLI. Synthesis of 9-Bora-10-oxa-phenanthrenes, Bis(2′-oxy-terphenylyl)halogenoboranes, and Bis(9-bora-10-oxa-phenanthrenyl)oxidesThe reaction of 2′-hydroxy-m-terphenyl and 2-hydroxy-biphenyl resp. with n-C4H9Li and Na resp. and subsequent addition of trihalogenoboranes yields 9-halogeno-9-bora-10-oxa-phenanthrenes 1, 2, 5 and A besides 9-2′-oxy-m-terphenylyl-9-bora-10-oxa-phenanthrene 3 and bis-(9-bora-10-oxa-phenanthrenyl)oxides 4 and 6. Under somewhat different reaction conditions one obtains also the bis(2′-oxy-terphenylyl)halogenoboranes 7 and 8, tris(2-oxy-biphenylyl)-borane 9 and t-butyl-chloro-(2-oxy-biphenylyl)borane 10. 11 results from reaction of 2 with lithated hexamethyldisilazane. The compounds are characterized analytically and spectroscopically (1H, 11B-nmr spectra; mass spectra). For 4 and 6 X-ray analyses were performed.
    Notes: Die Reaktion von lithiiertem bzw. natriiertem 2′-Hydroxy-m-terphenyl bzw. 2-Hydroxy-biphenyl mit Trihalogenboranen ergibt neben den 9-Halogeno-9-bora-10-oxaphenanthrenen 1, 2, 5 und A, 9-2′-Oxy-m-terphenylyl-9-bora-10-oxa-phenanthren 3, die Bis(9-bora-10-oxa-phenanthrenyl)oxide 4 und 6. Durch etwas veränderte Reaktionsbedingungen sind auch die Bis(2′-oxy-terphenylyl)-halogenoborane 7 und 8, Tris(2-oxy-biphenylyl)boran 9 und t-Butyl-chloro-(2-oxy-biphenylyl)boran 10 erhältlich. 11 erhält man durch Reaktion von 2 mit lithiiertem Hexamethyldisilazan. Die Verbindungen werden analytisch und spektroskopisch (1H, 11B-NMR; MS) charakterisiert. Von 4 und 6 wurden Röntgenstrukturen angefertigt.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 26 (1988), S. 501-506 
    ISSN: 0749-1581
    Keywords: Cyclic depsipeptide ; Inverse COLOC ; Inverse HMQC ; Semi-selective excitation ; NMR assignments in peptides ; Didemnin ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several one- and two-dimensional techniques have been used to assign the 1H and 13C NMR spectra of the cyclic heptadepsipeptide didemnin A in DMSO. The composition and sequence of the amino acid residues was known beforehand and could be confirmed by heteronuclear proton-carbon long-range couplings using the COLOC experiment and a recently proposed new inverse technique using Gaussian-shaped pulses. The aliphatic methyl resonances of the isostatin, hydroxyisovalerylpropionyl, N-methylleucine and leucine residues were assigned by means of the TOCSY and NOESY techniques. Aliphatic carbon assignment was performed by inverse correlation via heteronuclear double quantum coherence.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 525 (1985), S. 54-66 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reaction of Thiazylfluoride with Multifunctional Nitrogen DerivativesFrom the reaction of NSF 1 with LiN(SiMe3)R′ (R′ = CMe3, SiMe3), linear [e. g. (Me3C—N=S=N—)2S (11), Me3C—N=S=N—CMe3 (14), Me3Si—N=S=N—SiMe3 (17), (Me3Si)2N—S—N=S=N—SiMe3 (19)] and cyclic thiazenes (S4N5F (22)) are isolated, (S3N4)n (23) is obtained in high yield from 1 and 17 (in the ratio 2:1). Possible structures for 23 are discussed; the reaction of 23 with AsF5 gives S4N4 · AsF5 (24) in a hitherto unknown modification. Possible reactions of the terminal SN groups are discussed and the structures of 11 and 24 are reported.
    Notes: Aus der Umsetzung von NSF 1 mit LiN(SiMe3)R′ (R′ = CMe3, SiMe3) werden lineare [z. B. (Me3C—N=S=N—)2S (11), Me3CNSNCMe3 (14), Me3SiNSNSiMe3 (17), (Me3Si)2N—S—N=S=N—SiMe3 (19)] und cyclische Thiazene (S4N5F (22)) isoliert, die Umsetzung von 1 mit 17 im Molverhältnis 2:1 liefert (S3N4)n (23) in hohen Ausbeuten. Strukturvorschläge für 23 werden diskutiert; die Umsetzung von 23 mit AsF5 liefert S4N4 · AsF5 (24) in einer bisher nicht bekannten Modifikation. Reaktionsmöglichkeiten der terminalen SN-Gruppe werden diskutiert und die Strukturuntersuchungen an 11 und 24 mitgeteilt.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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