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Reactions of benzothiohydrazide as a bidentate nucleophile
Author(s) -
Elliott Arthur J.
Publication year - 1981
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.5570180434
Subject(s) - chemistry , nucleophile , denticity , medicinal chemistry , organic chemistry , computational chemistry , stereochemistry , catalysis , crystal structure
Benzothiohydrazide acts as a 1,4‐bidentate nucleophile under basic conditions, and condenses with suitably substituted pyridines, pyrimidines and quinoxalines to yield ring‐fused‐1,3,4‐thiadiazines un‐substituted on the 4‐nitrogen position.