Premium
1,2,4‐Triazoles. XXV. The effect of pyridine substitution on the isomerization of s ‐Triazolo[4,3‐ a ] pyridines into s ‐Triazolo[1,5‐ a ] pyridines
Author(s) -
Potts K. T.,
Surapaneni C. R.
Publication year - 1970
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.5570070504
Subject(s) - chemistry , isomerization , pyridine , ring (chemistry) , medicinal chemistry , nitro , substitution (logic) , stereochemistry , organic chemistry , catalysis , computer science , programming language , alkyl
The isomerization of s ‐triazolo[4,3‐ a ]pyridines into s ‐triazolo[1,5‐ a ]pyridines is greatly facilitated by electron withdrawing nitro substituents in the pyridine ring and retarded by electron donating amino groups.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom