The amidine rearrangement in 5-amino-6-aryl-1,2,4-triazine-4-oxides initiated by hydroxylamine

Authors
Chupakhin, ON Kozhevnikov, VN Prokhorov, AM Kozhevnikov, DN Rusinov, VL
Citation
On. Chupakhin et al., The amidine rearrangement in 5-amino-6-aryl-1,2,4-triazine-4-oxides initiated by hydroxylamine, TETRAHEDR L, 41(38), 2000, pp. 7379-7382
Citations number
7
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
41
Issue
38
Year of publication
2000
Pages
7379 - 7382
Database
ISI
SICI code
0040-4039(20000916)41:38<7379:TARI5I>2.0.ZU;2-L
Abstract
Addition of hydroxylamine at the 3 position of 6-aryl-5-amino-1,2,4-triazin e-4-oxides initiates the amidine rearrangement resulting in 6-aryl-5-hydrox ylamine-1,2,4-triazines, as confirmed by an experiment with N-15-labeling. (C) 2000 Published by Elsevier Science Ltd.