Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Rep. of Korea.
Angew Chem Int Ed Engl. 2017 Sep 11;56(38):11584-11588. doi: 10.1002/anie.201705829. Epub 2017 Aug 7.
Reported herein is an efficient copper(I)-catalytic system for the diastereo- and enantioselective 1,2-addition of 1,1-bis[(pinacolato)boryl]alkanes to protected imines to afford synthetically valuable enantioenriched β-aminoboron compounds bearing contiguous stereogenic centers. The reaction exhibits a broad scope with respect to protected imines and 1,1-bis[(pinacolato)boryl]alkanes, thus providing β-aminoboronate esters with excellent diastereo- and enantioselectivity. The synthetic utility of the obtained β-aminoboronate ester was also demonstrated.
本文报道了一种高效的铜(I)催化体系,用于对保护的亚胺进行 1,2-加成反应,以合成具有相邻手性中心的具有合成价值的对映体富集的β-氨基硼化合物。该反应对保护的亚胺和 1,1-双[(频哪醇)硼基]烷烃具有广泛的适用性,因此提供了具有优异的非对映选择性和对映选择性的β-氨基硼酸盐酯。还证明了获得的β-氨基硼酸盐酯的合成实用性。