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手性联萘基仲胺催化的醛的直接不对称溴化反应:高对映选择性和非对映选择性一锅法合成溴代醇。

Direct asymmetric bromination of aldehydes catalyzed by a binaphthyl-based secondary amine: highly enantio- and diastereoselective one-pot synthesis of bromohydrins.

机构信息

Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan.

出版信息

Chem Commun (Camb). 2010 Oct 28;46(40):7590-2. doi: 10.1039/c0cc02739a. Epub 2010 Sep 10.

DOI:10.1039/c0cc02739a
PMID:20830441
Abstract

One-pot stereoselective synthesis of bromohydrins as a useful chiral building block was achieved by the reaction of Grignard reagents with optically active α-bromoaldehydes, which were in situ generated by direct asymmetric bromination of aldehydes catalyzed by a binaphthyl-based secondary amine (S)-3.

摘要

一锅法立体选择性合成溴代醇作为一种有用的手性砌块,是通过格氏试剂与光学活性的α-溴代醛反应实现的,α-溴代醛是由手性联萘酚衍生的二级胺(S)-3 催化的醛的不对称直接溴化原位生成的。

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