z-logo
Premium
v ‐Triazolines. Part XIX . Thiocino[4,5‐ d ]‐1,2,3‐triazole and thiocino[4,5‐ d ]isoxazole derivatives
Author(s) -
Almirante Nicoletta,
Forti Luciana
Publication year - 1984
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.5570210438
Subject(s) - chemistry , isoxazole , nitrile , aryl , medicinal chemistry , organic chemistry , alkyl
5‐Amino‐2,3,6,7‐tetrahydrothiocines were reacted with arylazides yielding 1‐aryl‐9a‐amino‐1,3a,4,5,7,8,9,9a‐octahydrothiocino[4,5‐ d ]‐1,2,3‐triazoles which could be deaminated to 1‐aryl‐1,4,5,7,8,9‐hexahydrothiocino‐[4,5‐ d ]‐1,2,3‐triazoles. Similarly, the above enamines yielded, with nitrile oxides, 3‐aryl‐9a‐amino‐3a,4,5,8,9,9a‐hexahydrothiocino[4,5‐ d ]isoxazoles which were transformed with acids into 3‐aril‐4,5,8,9‐tetrahydrothiocino‐[4,5‐ d ]isoxazoles.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom