N-Heterocyclic carbene promoted enantioselective desymmetrization reaction of diarylalkane-bisphenols

被引:14
作者
Li, Shoulei [1 ]
Liu, Bin [1 ]
Chen, Li [1 ]
Li, Xin [1 ]
Cheng, Jin-Pei [1 ]
机构
[1] Nankai Univ, State Key Lab Elementoorgan Chem, Collaborat Innovat Ctr Chem Sci & Engn, Tianjin 300071, Peoples R China
关键词
FREE-ENERGY RELATIONSHIP; CHIRAL BUILDING-BLOCKS; ASYMMETRIC CATALYSIS; STERIC PARAMETERS; QUATERNARY STEREOCENTERS; NONCOVALENT INTERACTIONS; ENANTIOMERIC EXCESS; KINETIC RESOLUTION; ALCOHOLS; TRIARYLMETHANES;
D O I
10.1039/c7qo01083d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An enantioselective NHC-catalyzed desymmetrization reaction of diarylalkane-bisphenols with aldehydes was reported with linear free energy relationships (LFERs) to correlate the enantioselectivities with the steric and electronic parameters. The reaction scope is substantial, and a wide range of aromatic and aliphatic aldehydes, as well as diarylalkane-bisphenols were tolerated under the reaction conditions. As a result, a series of diarylalkane-bisphenol products were generated with excellent reactivities and enantioselectivities (up to 99% yield and up to 98.7:1.3 er). Furthermore, the reaction can be scaled up, and the desired product can be easily converted to valuable structures.
引用
收藏
页码:1101 / 1107
页数:7
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