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

O. N. Chupakhin, V. N. Kozhevnikov, A. M. Prokhorov, D. N. Kozhevnikov, V. L. Rusinov*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

13 Citations (Scopus)

Abstract

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 15N-labeling. (C) 2000 Published by Elsevier Science Ltd.

Original languageEnglish
Pages (from-to)7379-7382
Number of pages4
JournalTetrahedron Letters
Volume41
Issue number38
Early online date13 Sept 2000
DOIs
Publication statusPublished - 16 Sept 2000
Externally publishedYes

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