The Diarylprolinol Silyl Ethers: Ten Years After

被引:265
作者
Donslund, Bjarke S. [1 ]
Johansen, Tore Kiilerich [1 ]
Poulsen, Pernille H. [1 ]
Halskov, Kim Soholm [1 ]
Jorgensen, Karl Anker [1 ]
机构
[1] Aarhus Univ, Dept Chem, DK-8000 Aarhus C, Denmark
关键词
aminocatalysis; diarylprolinol silyl ethers; organocatalysis; DIELS-ALDER REACTION; ORGANOCATALYTIC CONJUGATE ADDITION; ASYMMETRIC ALPHA-AMINATION; HIGHLY ENANTIOSELECTIVE SYNTHESIS; ALPHA; BETA-UNSATURATED ALDEHYDES; ONE-POT; MICHAEL ADDITION; TRANSITION-METAL; MANNICH REACTION; AMINE CATALYSIS;
D O I
10.1002/anie.201503920
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Asymmetric organocatalysis has experienced an incredible development since the beginning of this century. The expansion of the field has led to a large number of efficient types of catalysts. One group, the diarylprolinol silyl ethers, was introduced in 2005 and has been established as one of the most frequently used in aminocatalysis. In this Minireview, we will take a look in the rear-view mirror, ten years after the introduction of the diarylprolinol silyl ethers. We will focus on the perspectives of the different activation modes made available by this catalytic system. Starting with a short introduction to aminocatalysis, we will outline the properties that have made the diarylprolinol silyl ethers a common choice of catalyst. Furthermore, we will describe the major tendencies in the activation and reaction concepts developed with regard to reactivity patterns and combinations with other activation concepts.
引用
收藏
页码:13860 / 13874
页数:15
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