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A Mild and Efficient Method for Selective Acetylation of Amines
Author(s) -
Yang ShyhChyun,
Wang HueyMin,
Chen LingChing
Publication year - 1995
Publication title -
journal of the chinese chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.329
H-Index - 45
eISSN - 2192-6549
pISSN - 0009-4536
DOI - 10.1002/jccs.199500078
Subject(s) - chemistry , acetylation , primary (astronomy) , organic chemistry , biochemistry , physics , astronomy , gene
Primary and secondary amines were acetylated under mild conditions by means of 3‐acetyl‐1,3‐thiazolidine‐2‐thione [ATT(1)]. The reaction was successfully applied to selective acetylation of a primary amino group of diamines containing a primary and a secondary amino groups or exclusive N ‐acetylation of amino alcohols.