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Ring transformation of condensed dihydro‐ as ‐triazines
Author(s) -
Berényi E.,
Benkó P.,
Zólyomi G.,
Tamás J.
Publication year - 1981
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.5570180809
Subject(s) - chemistry , ring (chemistry) , quinoline , transformation (genetics) , triazine , aqueous medium , aqueous solution , medicinal chemistry , stereochemistry , polymer chemistry , organic chemistry , biochemistry , gene
The 2‐amino‐ as ‐triazino[6,5‐ c ]quinoline as well as 3‐aminopyrido[4,3‐ e ]‐ as ‐triazine had previously been synthetized by Berényi (1) and Benkó et al (2). In this paper, the ring transformation occuring in aqueous media of the dihydro intermediates and their salts, respectively appearing during the synthesis of 2‐substitutedamino‐ as ‐triazino[6,5‐ c ]quinolines, are reported.