Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan.
Chem Commun (Camb). 2010 Oct 28;46(40):7590-2. doi: 10.1039/c0cc02739a. Epub 2010 Sep 10.
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.
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。