Hexahydropyrrolo [2,3-b]indoles: A new class of structurally rigid tricyclic skeleton for oxazaborolidine-catalyzed asymmetric borane reduction

Jian Xiao, Zhen Zhou Wong, Yun Peng Lu, Teck Peng Loh

科研成果: 期刊稿件文章同行评审

15 引用 (Scopus)

摘要

A new class of structurally rigid tricyclic chiral ligands based on the hexahydropyrrolo [2,3b]indole skeleton has been rationally designed and the catalytic abilities in asymmetric catalysis have been shown in the enantioselective borane reduction of prochiral ketones to afford the chiral alcohols in excellent yields and high enantioselectivities (up to 97% ee).

源语言英语
页(从-至)1107-1112
页数6
期刊Advanced Synthesis and Catalysis
352
7
DOI
出版状态已出版 - 3 5月 2010
已对外发布

指纹

探究 'Hexahydropyrrolo [2,3-b]indoles: A new class of structurally rigid tricyclic skeleton for oxazaborolidine-catalyzed asymmetric borane reduction' 的科研主题。它们共同构成独一无二的指纹。

引用此