Anionic hetero[3,3] and [3,5][ rearrangements of hydroxylamine derivatives accompanied with N-O bond cleavage

DOI: 10.1055/s-1994-25645

Source and publish data:

Synthesis p. 1096 - 1105 (1994)

Update date:2022-08-06

Topics: N-O Bond Cleavage Hydroxylamine derivatives

Authors:

Endo Endo

Uchida Uchida

Hizatate

Shudo Shudo

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Article abstract of DOI:10.1055/s-1994-25645

Aromatic and aliphatic N,O-divinylhydroxylamine systems generated in situ from hydroxylamine derivatives smoothly undergo [3,3] rearrangement. The base-catalyzed formation and rearrangement of enolates or dienolates of N-aryl-O-acylhydroxylamines, N,O-dia

Full text of DOI:10.1055/s-1994-25645

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