Issue 1, 2000

Cleavage of the N–O bond in substituted hydroxylamines under basic conditions

Abstract

The cleavage of the N–O bond in hydroxylamines R1NR–OR2 accompanied by oxidation of the adjacent carbon is directed by the CH acidity of R1 and R2 groups.

Article information

Article type
Paper

Mendeleev Commun., 2000,10, 32-34

Cleavage of the N–O bond in substituted hydroxylamines under basic conditions

K. V. Nikitin and N. P. Andryukhova, Mendeleev Commun., 2000, 10, 32 DOI: 10.1070/MC2000v010n01ABEH001206

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