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

Kazuhiko Takai; Noriko Katsura; Yuji Kunisada

doi:10.1039/b105357b

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

Kazuhiko Takai, Noriko Katsura, Yuji Kunisada

Research output: Contribution to journal › Article › peer-review

19 Citations (Scopus)

Abstract

Chromioenamines can be generated by treatment of Oacetyloximes with chromium(II) via two steps of one-electron reduction and successive isomerization, and the species react with aldehydes to give g-amino alcohols after reduction with LiAlH₄.

Original language	English
Pages (from-to)	1724-1725
Number of pages	2
Journal	Chemical Communications
Volume	1
Issue number	18
DOIs	https://doi.org/10.1039/b105357b
Publication status	Published - Jan 1 2001

ASJC Scopus subject areas

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
Chemistry(all)
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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

abstract = "Chromioenamines can be generated by treatment of Oacetyloximes with chromium(II) via two steps of one-electron reduction and successive isomerization, and the species react with aldehydes to give g-amino alcohols after reduction with LiAlH4.",

author = "Kazuhiko Takai and Noriko Katsura and Yuji Kunisada",

year = "2001",

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doi = "10.1039/b105357b",

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AU - Takai, Kazuhiko

AU - Katsura, Noriko

AU - Kunisada, Yuji

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Y1 - 2001/1/1

N2 - Chromioenamines can be generated by treatment of Oacetyloximes with chromium(II) via two steps of one-electron reduction and successive isomerization, and the species react with aldehydes to give g-amino alcohols after reduction with LiAlH4.

AB - Chromioenamines can be generated by treatment of Oacetyloximes with chromium(II) via two steps of one-electron reduction and successive isomerization, and the species react with aldehydes to give g-amino alcohols after reduction with LiAlH4.

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JO - Chemical Communications

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

Abstract

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