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On Triazoles. VI . The acylation of 5‐amino‐1,2,4‐triazoles
Author(s) -
Reiter József,
Pongó László,
Dvortsák Péter
Publication year - 1987
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.5570240126
Subject(s) - chemistry , tautomer , acylation , ring (chemistry) , 1,2,4 triazole , stereochemistry , triazole , medicinal chemistry , combinatorial chemistry , organic chemistry , catalysis
The isomeric and tautomeric structure of I and II type monoacylated 5‐amino‐1,2,4‐triazole derivatives was studied with the help of their ir, uv, pmr and cmr spectra as well as model compounds prepared for this purpose. It was stated that the structure of the I type ring‐acylated derivatives is 2o and those of their II type isomers is 5a .