Author:
Bartels-Keith James R.,Cieciuch Ronald F. W.
Abstract
Certain ortho-substituted acetanilides exhibit proton magnetic resonance signals at unusually low field for the amido proton and the aromatic proton adjacent to the acetamido group. This effect, explicable in terms of intramolecular hydrogen-bonding, has been observed for nitro, carbonyl, sulfamoyl, and sulfonyl substituents. Solvent effects are discussed.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
31 articles.
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