Premium
Selenium heterocycles. XXXV . Synthesis and pyrrolysis of aryloxy‐, arylthio‐, and arylseleno‐1,2,3‐selenadiazoles
Author(s) -
Shafiee A.,
Toghraie S.,
Aria F.,
MortezaeiZandjani G.
Publication year - 1982
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.5570190609
Subject(s) - chemistry , selenium , organic chemistry
A series of 4‐substituted‐5‐arylthio‐1,2,3‐selenadiazoles, 4‐substituted‐5‐arylseleno‐1,2,3‐selenadiazoles and 4‐aryloxymethyl‐1,2,3‐selenadiazoles were synthesized. Pyrrolysis of these compounds afforded the corresponding acetylenes XI, XIII (X = S, Se) and XII, respectively. Oxidation of 4‐substituted‐5‐arylthio‐1,2,3‐selenadiazoles (XIV) with m ‐chloroperbenzoic acid gave 4‐substituted‐5‐arylsulfinyl‐1,2,3‐selenadiazoles (XV) and 4‐substituted‐5‐arylsulfonyl‐1,2,3‐selenadiazoles (XVI).
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