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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 98 (1994), S. 12933-12937 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Structural chemistry 10 (1999), S. 47-52 
    ISSN: 1572-9001
    Keywords: Alkylidenphthalan ; isobenzofuran ; semiempirical calculations ; density functional theory
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Semiempirical (AM1, PM3) and density functional theoretical studies (B3LYP/6-31G*) are reported for the tautomerism of 2-methylidene-2,5-dihydrofurans (3a–e) and the corresponding 2-methylfurans (4a–e) and of benzannulated derivatives (5a–e, 6a–e, 7–14).
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 100 (1967), S. 1550-1558 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Synthese von verschiedenen N-substituierten 2-Hydroxy-3-methoxy-morphinanen aus den entsprechenden Isochinolinvorstufen nach dem Prinzip des Morphinanringschlusses wird beschrieben. Dabei erweist sich ein bestimmtes Schwefelsäure/Äther-Gemisch zur Cyclisierung von N-Acylverbindungen besonders geeignet. In allen Fällen entstehen auch die isomeren 4-Hydroxy-3-methoxy-morphinane als Nebenprodukte, und zu diesen gehört das racem. Dihydrothebainon.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 101 (1968), S. 1190-1194 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aus den 1-Veratryl-isochinolinen 6 lassen sich unter milden Bedingungen die 2.3-Dimetoxy-6-keto-morphinane 9 in guter Ausbeute darstellen.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 101 (1968), S. 3313-3325 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aus der Chinasäure werden nach verschiedenen Verfahren durch Verlängerung der Seitenkette und Dehydrierung einer Hydroxylgruppe das 5-Dehydro-β-chinoäthylamin und die beiden epimeren 5-Dehydro-β-chinoäthanolamine dargestellt. Diese Verbindungen gehen unter„zellmöglichen“ Bedingungen in ihre physiologisch aktiven Aromatisierungsprodukte Dopamin und (-)- bzw. (+)-Noradrenalin über.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 100 (1967), S. 1-8 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Verbindung 1, das salzartige Primärprodukt einer Bischler-Napieralsky-Synthese, läßt sich in einem Schritt in 75-proz. Ausbeute zur sekundären Phenolbase 4 reduzieren. Von hier aus sind zahlreiche 1-substituierte Hydroisochinolon-Derivate zugänglich.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 31-47 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reaction of o-Benzoquinone Diimines with KetenesN, N′-Dibenzoyl- and N, N′-bis(phenylsulfonyl)-o-benzoquinone diimines react with diphenyl-and bis(p-nitrophenyl)ketene, resp., to yield 3,4-dihydro-2(1H)-quinoxalinones. Investigations concerning the mechanism (solvent dependence, influence of substituents, activation parameters) are in accord with the assumption, that this reaction belongs to a type of cycloaddition with an only moderate polar transition state, in which the diimine acts as an electron-deficient and the ketene as an electron-rich reactant.
    Notes: N, N′-Dibenzoyl- und N, N′-Bis(phenylsulfonyl)-o-benzochinon-diimine reagieren mit Diphenyl- bzw. Bis (p-nitrophenyl)keten unter Bildung von 3,4-Dihydro-2(1H)-chinoxalinonen. Untersuchungen zum Mechanismus (Lösungsmittel- und Substituentenabhängigkeit, Aktivierungsparameter) stehen mit der Annahme in Einklang, daß eine Mehrzentrencycloaddition mit nur wenig polarem Übergangszustand vorliegt, bei der die Diiminkomponente als elektronenärmerer und die Ketenkomponente als elektronenreicherer Reaktionspartner fungiert.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0170-2041
    Keywords: Thieno[2,3-c]furan ; Cycloaddition, intramolecular ; Benzothiophene ; Marmelerin, thiophene analogue of ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Intramolecular Cycloaddition Reactions with Isobenzofurans, V1). - Synthesis of rac-Thiamarmelerin, a Thiophene Analogue of a Naturally Occurring Furanosesquiterpenerac-Thiamarmelerin (7b) is prepared by an intramolecular Diels-Alder reaction of a thieno[2,3-c]furan.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of Mesoionic Five-membered Heterocycles with o-Quinonoid Compounds, II1).  -  A Contribution to the Problem of Ketene Tautomers of 1,3-Oxazolium-5-olates1,3-Oxazolium-5-olates acylated at C-4 react with tetrachloro-o-benzoquinone (9) to give 2,3-dihydro-1,4-benzodioxin-2-ones 10 which can formally be derived from the valence tautomeric ketenes 2. There is evidence for the assumption that ketenes are not involved in these reactions as intermediates. Furthermore, the products 15a, b which probably result from [4 + 4] cycloadducts formed primarily, have been isolated. Oxazolo[3,2-a]pyridinium-2-olates 8 acylated at C-3 react with 9 to give 1:2 adducts 20.
    Notes: C-4-acylierte 1,3-Oxazolium-5-olate reagieren mit Tetrachlor-o-benzochinon (9) unter Bildung von 2,3-Dihydro-1,4-benzodioxin-2-onen 10, die sich formal von den valenztautomeren Ketenen 2 ableiten. Es wird ein Hinweis darauf erhalten, daß Ketene bei diesen Umsetzungen nicht ais Zwischenprodukte auftreten. Weiterhin werden die Produkte 15a, b isoliert, die möglicherweise aus primär gebildeten [4 + 4]-Cycloaddukten entstehen. C-3-acylierte Oxazolo[3,2-a]pyridinium-2-olate 8 liefern mit 9 die 1:2-Addukte 20.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Mesoionic Six-membered Heterocycles, III.  -  Reactions of o-Quinonoid Compounds with 6-Oxo-6H-1,3-diazin-1-ium-4-olatesMesoionic 6-oxo-6H-1,3-diazin-1-ium-4-olates 9 react with tetrachloro-o-benzoquinone (2, R = Cl) to give 1:1 adducts 12 which can formally be derived from ketene tautomers 13 of 9. The structure of 12f has been clarified by X-ray crystallography.
    Notes: Mesoionische 6-Oxo-6H-1,3-diazin-1-ium-4-olate 9 reagieren mit Tetrachlor-o-benzochinon (2, R = Cl) unter Bildung von 1:1-Addukten 12, die sich formal von den Ketentautomeren 13 von 9 ableiten. Die Struktur von 12f wurde durch eine Röntgenstrukturanalyse geklärt.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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