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  • 1975-1979  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1979 (1979), S. 689-700 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Dithiacyclopentenes, XXXIII. - Reactions of 1,3-Dithiole-2-thiones with N-Chloramides4-Phenyl-1,3-dithiole-2-thione (1a) and 2-thioxo-1,3-dithiole-4,5-dicarbonitrile (1c) react with N,N-dichloroamides - N,N-dichlorobenzenesulfonamides 2-4, N,N-dichlorosulfamides 5, 6, N,N-dichloroethylurethane (7), N,N-dichloro-o-nitrobenzamide (8) - to give N-(1,3-dithiol)-2-ylidene)amides 17-23.
    Notes: 4-Phenyl-1,3-dithiol-2-thion (1a) und 2-Thioxo-1,3-dithiol-4,5-dicarbonitril (1c) reagieren mit N,N-Dichloramiden - N,N-Dichlorbenzolsulfonamide 2-4, N,N-Dichlorsulfamide 5,6, N,N-Dichlorethylurethan (7), N,N-Dichlor-o-nitrobenzamid (8) - zu den N-(1,3-Dithiol,2-yliden)-amiden 17-23.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1978 (1978), S. 387-397 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 1,2-Dithiacyclopentenes, XXXII1).  -  Reactions of 3H-1,2-Dithiole-3-thiones with N-Chlorobenzamides5-Phenyl-3H-1,2-dithiole-3-thione (2) reacts with N,N-dichlorobenzamides 3 to give N-(3 H-1,2-dithiol-3-ylidene)benzamides 11 and 12 and with N-chlorobenzamides 1 to give N-benzoyl-S-(3H-1,2-dithiol-3-ylidene)sulfimides 7, respectively, which, on extrusion of sulfur, yield N-ylidenebenzamides 11. The mechanism has been studied.
    Notes: 5-Phenyl-3H-1,2-dithiol-3-thion (2) reagiert mit N,N-Dichlorbenzamiden 3 zu N-(3 H-1,2-Dithiol-3-yliden)benzamiden 11 und 12, mit N-Chlorbenzamiden 1 zu N-Benzoyl-S-(3H-1,2-dithiol-3-yliden)sulfimiden 7, die unter Schwefelabspaltung N-Ylidenbenzamide 11 liefern. Der Mechanismus wurde untersucht.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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