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The sulfenylation of substituted imines
Author(s) -
Seitz David E.,
Needham FangLing
Publication year - 1983
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570200359
Subject(s) - chemistry , electrophile , imide , solvent , product distribution , organic chemistry , medicinal chemistry , base (topology) , catalysis , mathematical analysis , mathematics
Abstract Conditions for mono‐ and bissulfenylation of N ‐methyl‐3,3‐dimethylpyrrolidine‐2,5‐dione are described and compared to a closely related six‐membered imide, N ‐methyl‐3‐ethyl‐3‐phenylpiperidine‐2,6‐dione. The influence of solvent, base and electrophile on product distribution is explored.