Author:
Hardstaff W. R.,Langler R. F.,Leahy J.,Newman M. J.
Abstract
An examination of the chlorination of phenylmethy), diphenylmethyl, and triphenylmethyl methylsulfonyl sulfides (1, 2, and 3) in aqueous acetic acid has provided indirect evidence for Pummerer rearrangement during the chlorination of an α-methylsulfonyl sulfinyl chloride. The results are discussed from both mechanistic and synthetic standpoints.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
20 articles.
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