Generation of chromioenamines by reduction of O-acetyloximes with chromium(II) and their application

Kazuhiko Takai, N. Katsura, Y. Kunisada

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

Chromioenamines can be generated by treatment of O-acetyloximes with chromium(II) via two steps of one-electron reduction and successive isomerization, and the species react with aldehydes to give γ-amino alcohols after reduction with LiA1H4.

Original languageEnglish
Pages (from-to)1724-1725
Number of pages2
JournalChemical Communications
Issue number18
Publication statusPublished - Sep 21 2001

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Chromium
Amino alcohols
Amino Alcohols
Isomerization
Aldehydes
Electrons

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Generation of chromioenamines by reduction of O-acetyloximes with chromium(II) and their application. / Takai, Kazuhiko; Katsura, N.; Kunisada, Y.

In: Chemical Communications, No. 18, 21.09.2001, p. 1724-1725.

Research output: Contribution to journalArticle

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