4.17 Asymmetric 1,2-Addition of Organometallics to Carbonyl and Imine Groups

S. Suga, M. Kitamura

研究成果

13 被引用数 (Scopus)

抄録

The development of asymmetric 1,2-additions of organometallics to carbonyl compounds and imines for the synthesis of chiral alcohols and amines has been overviewed. The highly enantioselective addition reactions of dialkylzincs to aldehydes developed in the mid-1980s have definitely played a key role in this field of chemistry. Hundreds of chiral sources which promote additions of zinc alkyl groups to aldehydes with high enantioselectivities have appeared in the literature, and the chemistry became one of the milestones of asymmetric catalysis in organic synthesis. The subsequent progress in the efficient catalytic asymmetric synthesis of tertiary alcohols by the reactions of ketones and organometallic reagents is also outstanding. Over the past decade, catalytic enantioselective synthesis of chiral amines using asymmetric 1,2-addition of organometallics to imines has become a matter of common knowledge.

本文言語English
ホスト出版物のタイトルSynthetic Methods III - Catalytic Methods
ホスト出版物のサブタイトルC-C Bond Formation
出版社Elsevier Ltd
ページ328-342
ページ数15
4
ISBN(印刷版)9780080951683
DOI
出版ステータスPublished - 9月 2012

ASJC Scopus subject areas

  • 化学 (全般)

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