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

doi:10.1016/S0040-4039(00)01245-4

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 journal › Article › peer-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 language	English
Pages (from-to)	7379-7382
Number of pages	4
Journal	Tetrahedron Letters
Volume	41
Issue number	38
Early online date	13 Sept 2000
DOIs	https://doi.org/10.1016/S0040-4039(00)01245-4
Publication status	Published - 16 Sept 2000
Externally published	Yes

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

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.",

author = "Chupakhin, \{O. N.\} and Kozhevnikov, \{V. N.\} and Prokhorov, \{A. M.\} and Kozhevnikov, \{D. N.\} and Rusinov, \{V. L.\}",

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T1 - The amidine rearrangement in 5-amino-6-aryl-1,2,4-triazine-4- oxides initiated by hydroxylamine

AU - Chupakhin, O. N.

AU - Kozhevnikov, V. N.

AU - Prokhorov, A. M.

AU - Kozhevnikov, D. N.

AU - Rusinov, V. L.

PY - 2000/9/16

Y1 - 2000/9/16

N2 - 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.

AB - 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.

UR - https://www.scopus.com/pages/publications/0034675231

U2 - 10.1016/S0040-4039(00)01245-4

DO - 10.1016/S0040-4039(00)01245-4

M3 - Article

AN - SCOPUS:0034675231

SN - 0040-4039

VL - 41

SP - 7379

EP - 7382

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 38

ER -

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

Abstract

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