Kitanosono Taku, Xu Pengyu, Isshiki Satoshi, Zhu Lei, Kobayashi Shū
Deparment of Chemistry, School of Science, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo, Japan.
Chem Commun (Camb). 2014 Aug 25;50(66):9336-9. doi: 10.1039/c4cc04062g.
Enantioselective conjugate addition of bis(pinacolato)diboron to α,β-unsaturated imines proceeds smoothly in water in the presence of a chiral copper(II) complex consisting of Cu(OAc)2 and chiral 2,2'-bipyridine. The corresponding β-boryl imines, which were oxidized to β-hydroxy imines, further leading to γ-amino alcohols, were obtained in high yields and high enantioselectivities.
在由醋酸铜(Cu(OAc)₂)和手性2,2'-联吡啶组成的手性铜(II)配合物存在下,双(频哪醇合)二硼与α,β-不饱和亚胺的对映选择性共轭加成在水中顺利进行。相应的β-硼基亚胺被氧化为β-羟基亚胺,进一步生成γ-氨基醇,产率和对映选择性都很高。