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Reductive cleavage of N-substituted benzenesulfonamides and p-sulfamylbenzoic acid

The objective of the present work was to study further the effect of varying substituents on the nitrogen atom and on the ring of sulfonamides in the Birch reduction of aromatic sulfonamides, especially with respect to the amount of thiol formed, in the hope that information concerning the initial cleavage step might be discerned.

Identiferoai:union.ndltd.org:pacific.edu/oai:scholarlycommons.pacific.edu:uop_etds-2868
Date01 January 1975
CreatorsDavenport, Robert E.
PublisherScholarly Commons
Source SetsUniversity of the Pacific
Detected LanguageEnglish
Typetext
Formatapplication/pdf
SourceUniversity of the Pacific Theses and Dissertations

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