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Nickel-catalyzed enantioselective 1,2-vinylboration of styrenes
Yang Ye1,2, Jiandong Liu3, Bing Xu1,2
1School of Pharmacy, Hangzhou Normal University Hangzhou Zhejiang 311121 PR China yeyang0711@163.com xbs@hznu.edu.cn xyye@hznu.edu.cn.
Abstract:
A novel nickel-catalyzed asymmetric 1,2-vinylboration reaction has been developed to afford benzylic alkenylboration products with high yields and excellent enantioselectivities by using a chiral bisoxazoline ligand. Under optimized conditions, a wide variety of chiral 2-boryl-1,1-arylvinylalkanes are efficiently prepared from readily available olefins and vinyl halides in the presence of bis(pinacolato)diboron as the boron source in a mild and easy-to-operate manner. This three-component cascade protocol furnishes exceptional chemo- and stereoselectivity, and its usefulness is illustrated by its application in asymmetric modifications of several structurally complex natural products and pharmaceuticals.
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