The amidine rearrangement in 5-amino-6-aryl-1,2,4-triazine-4-oxides initiated by hydroxylamine
摘要:
Addition of hydroxylamine at the 3 position of 6-aryl-5-amino-1,2,4-triazine-4-oxides initiates the amidine rearrangement resulting in 6-aryl-5-hydroxylamine-1,2,4-triazines, as confirmed by an experiment with N-15-labeling. (C) 2000 Published by Elsevier Science Ltd.
Nucleophile-induced transformations of 1,2,4-triazines. 3. Anrorc constriction of the ring in the reaction of 6-aryl-3-dimethylamino-1,2,4-triazine 4-oxides with KCN
作者:V. N. Kozhevnikov、D. N. Kozhevnikov、V. L. Rusinov、O. N. Chupakhin
DOI:10.1007/bf02319336
日期:1999.4
Chupakhin; Kozhevnikov; Kozhevnikov, Russian Journal of Organic Chemistry, 1998, vol. 34, # 3, p. 388 - 392
作者:Chupakhin、Kozhevnikov、Kozhevnikov、Rusinov
DOI:——
日期:——
The amidine rearrangement in 5-amino-6-aryl-1,2,4-triazine-4-oxides initiated by hydroxylamine
作者:Oleg N Chupakhin、Valery N Kozhevnikov、Anton M Prokhorov、Dmitry N Kozhevnikov、Vladimir L Rusinov
DOI:10.1016/s0040-4039(00)01245-4
日期:2000.9
Addition of hydroxylamine at the 3 position of 6-aryl-5-amino-1,2,4-triazine-4-oxides initiates the amidine rearrangement resulting in 6-aryl-5-hydroxylamine-1,2,4-triazines, as confirmed by an experiment with N-15-labeling. (C) 2000 Published by Elsevier Science Ltd.