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协同硫脲-Bronsted 酸有机催化:TMSCN 对醛的对映选择性氰硅烷化反应。

Cooperative thiourea-Brønsted acid organocatalysis: enantioselective cyanosilylation of aldehydes with TMSCN.

机构信息

Institute of Organic Chemistry, Justus-Liebig University, Heinrich-Buff-Ring 58, 35392 Giessen, Germany.

出版信息

J Org Chem. 2011 Dec 2;76(23):9764-76. doi: 10.1021/jo201864e. Epub 2011 Nov 7.

Abstract

We report a new thiourea-Brønsted acid cooperative catalytic system for the enantioselective cyanosilylation of aldehydes with yields up to 90% and enantioselectivities up to 88%. The addition of an achiral acid was found to be crucial for high asymmetric induction. Mechanistic investigations using a combination of NMR, ESI-MS, and density functional theory computations (including solvent corrections) at the M06/6-31G(d,p) level of theory suggest that the key catalytic species results from the cooperative interaction of bifunctional thioureas and an achiral acid that form well-defined chiral hydrogen-bonding environments.

摘要

我们报道了一种新型硫脲-Bronsted 酸协同催化体系,用于醛的对映选择性氰硅烷化反应,产率高达 90%,对映选择性高达 88%。发现添加非手性酸对于高不对称诱导至关重要。使用 NMR、ESI-MS 和密度泛函理论计算(包括溶剂校正)的组合进行的机理研究表明,关键的催化物种是由双功能硫脲和非手性酸的协同相互作用形成的,形成了定义明确的手性氢键环境。

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