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砜的不对称有机催化。

Asymmetric organocatalysis with sulfones.

机构信息

Center for Catalysis, Department of Chemistry, Aarhus University, 8000 Aarhus C, Denmark.

出版信息

Angew Chem Int Ed Engl. 2010 Apr 1;49(15):2668-79. doi: 10.1002/anie.200906340.

Abstract

Asymmetric organocatalysis has become a powerful tool for the synthesis of optically active compounds. Whereas early research mainly focused on combining simple reagents as a proof-of-concept for asymmetric organocatalysis, recent investigations are directed towards extending the concept to more target- and diversity-oriented synthesis. As a result of the many transformation possibilities and their ability to generate both nucleophilic and electrophilic reaction partners, sulfones have become especially important substrates in the field of organocatalysis.

摘要

不对称有机催化已成为合成光学活性化合物的有力工具。虽然早期的研究主要集中在将简单试剂组合在一起,作为不对称有机催化的概念验证,但最近的研究方向是将这一概念扩展到更具目标性和多样性的合成。由于亚砜具有许多转化可能性,并且能够生成亲核和亲电反应试剂,因此它们已成为有机催化领域中特别重要的底物。

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