Titanium-catalyzed enantioselective additions of alkyl groups to aldehydes: Mechanistic studies and new concepts in asymmetric catalysis

被引:132
作者
Walsh, PJ [1 ]
机构
[1] Univ Penn, Dept Chem, P Roy & Diane T Vagelos Labs, Philadelphia, PA 19104 USA
关键词
DIELS-ALDER REACTIONS; CRYSTAL-STRUCTURES; ACHIRAL LIGANDS; SOLID-STATE; COMPLEXES; REAGENTS; ALCOHOLS; TADDOLS; DISULFONAMIDE; OPTIMIZATION;
D O I
10.1021/ar0300219
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The catalytic asymmetric addition of alkyl groups to aldehydes is an important reaction in the enantioselective synthesis of secondary alcohols. This reaction can be catalyzed by zinc- or titanium-based catalysts. While the mechanism of the zinc/amino alcohol catalysts has received significant attention, the titanium-based catalysts have been less studied. This Account summarizes our mechanistic studies with bis(sulfonamide) and BINOL-derived titanium catalysts. It also describes our use of this reaction in the development of new approaches to asymmetric catalysis, including applications of diastereomeric catalysts and optimization of asymmetric catalysts with achiral and meso ligands.
引用
收藏
页码:739 / 749
页数:11
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