Department of Chemistry, School of Science, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo, Japan.
Chem Soc Rev. 2018 Jun 18;47(12):4388-4480. doi: 10.1039/c7cs00824d.
Recent developments in catalytic asymmetric aldol reactions have been summarized. Enantioselective aldol reactions are important methods to synthesize β-hydroxy carbonyl compounds in optical pure form, and as such, numerous successful chiral catalysts were designed and applied for asymmetric aldol reactions. This review article is organized under the categories of: (1) catalytic enantioselective aldol reactions of preformed enolates, (2) catalytic enantioselective direct-type aldol reactions using chiral metal catalysts, (3) catalytic enantioselective direct-type aldol reactions using organocatalysts, (4) catalytic enantioselective aldol reactions in aqueous media. Examples of the aldol reactions that employ simple carbonyl compounds will be also the focus of this review.
综述了催化不对称羟醛反应的最新进展。对映选择性羟醛反应是合成光学纯β-羟基羰基化合物的重要方法,因此,设计并应用了许多成功的手性催化剂用于不对称羟醛反应。本文综述按以下类别进行组织:(1) 预形成烯醇盐的催化对映选择性羟醛反应,(2) 使用手性金属催化剂的催化对映选择性直接型羟醛反应,(3) 使用有机催化剂的催化对映选择性直接型羟醛反应,(4) 在水相中的催化对映选择性羟醛反应。本综述还将重点介绍使用简单羰基化合物的羟醛反应实例。