Asymmetric vinylogous Mukaiyama aldol reactions using vinylketene N,O-acetals in total syntheses of natural products

Seijiro Hosokawa, Kuniaki Tatsuta

研究成果: Review article

53 引用 (Scopus)

抜粋

Asymmetric vinylogous aldol reaction is a powerful methodology to introduce a multi functional group in the stereoselective manner. Recently, we have developed highly stereoselective vinylogous Mukaiyama aldol reactions using vinylketene N,O-acetals possessing the chiral oxazolidone. Our methodology has been applied to the asymmetric syntheses of natural products to establish the short and efficient routes. This review focuses on the asymmetric vinylogous Mukaiyama aldol reactions using vinylketene N,O-acetals in total syntheses of natural products.

元の言語English
ページ(範囲)1-18
ページ数18
ジャーナルMini-Reviews in Organic Chemistry
5
発行部数1
DOI
出版物ステータスPublished - 2008 2 1

ASJC Scopus subject areas

  • Organic Chemistry

フィンガープリント Asymmetric vinylogous Mukaiyama aldol reactions using vinylketene N,O-acetals in total syntheses of natural products' の研究トピックを掘り下げます。これらはともに一意のフィンガープリントを構成します。

  • これを引用