z-logo
Premium
Photochemical cyclization of some aldehyde thiosemicarbazones
Author(s) -
Gruttadauria Michelangelo,
Buccheri Francesco,
Buscemi Silvestre,
Cusmano Giuseppe,
Noto Renato,
Werber Giuseppe
Publication year - 1992
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.5570290142
Subject(s) - chemistry , aldehyde , methanol , ring (chemistry) , semicarbazone , medicinal chemistry , photochemistry , organic chemistry , catalysis
The photochemical behaviour of some substituted aldehyde thiosemicarbazones 1a‐k has been investigated in methanol at 254 nm. Thiosemicarbazones of glyoxil methyl ester 1a‐f cyclized to furnish the 3‐thioxo‐ 1,2,4‐triazin‐5‐one 2 ring system. The remaining thiosemicarbazones 1g‐j gave 1,2,4‐triazoline 4 derivatives.

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