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用于不对称直接羟醛缩合反应的酸碱催化设计

Design of acid-base catalysis for the asymmetric direct Aldol reaction.

作者信息

Saito Susumu, Yamamoto Hisashi

机构信息

Institute for Advanced Research & Graduate School of Science, Nagoya University, Chikusa, Nagoya 464-8602, Japan.

出版信息

Acc Chem Res. 2004 Aug;37(8):570-9. doi: 10.1021/ar030064p.

Abstract

Proper design of acid-base catalysis has been shown to be effective for achieving high reactivity and selectivity in the asymmetric direct aldol reaction during the development of diamine-Brønsted acid types of catalyst. In this study, two principal approaches have been implemented to create a new type of catalysis and high catalytic efficiency: one is the creation of a highly viable acidic function within acid-base catalysts; the other is the creation of rather complicated but more cooperatively arranged hydrogen-bond networks that would be expected to stabilize a transition state, thereby promoting new reactivity and selectivity.

摘要

在二胺-布朗斯特酸型催化剂的开发过程中,酸碱催化的合理设计已被证明对在不对称直接羟醛反应中实现高反应活性和选择性是有效的。在本研究中,已采用两种主要方法来创建新型催化作用和高催化效率:一种是在酸碱催化剂内创建高度可行的酸性官能团;另一种是创建相当复杂但排列更协同的氢键网络,预计该网络可稳定过渡态,从而促进新的反应活性和选择性。

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