Synthesis of Axially Chiral Aldehydes by N-Heterocyclic-Carbene-Catalyzed Desymmetrization Followed by Kinetic Resolution

被引:74
作者
Wu, Yingtao [1 ]
Li, Mingrui [1 ]
Sun, Jiaqiong [2 ]
Zheng, Guangfan [1 ]
Zhang, Qian [1 ,3 ]
机构
[1] Northeast Normal Univ, Dept Chem, Jilin Prov Key Lab Organ Funct Mol Design & Synth, Changchun 130024, Peoples R China
[2] Northeast Normal Univ, Sch Environm, Changchun 130117, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organomet Chem, 345 Lingling Rd, Shanghai 200032, Peoples R China
关键词
Axially Chiral Aldehydes; Desymmetrization; Esterification; Kinetic Resolution; N-Heterocyclic Carbenes; ENANTIOSELECTIVE SYNTHESIS; ATROPOSELECTIVE SYNTHESIS; BRONSTED ACID; ATROPISOMERS; ALCOHOLS; ESTERS; ALKYLATION; OXIDATIONS; CHALLENGE; HYDROGEN;
D O I
10.1002/anie.202117340
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Axially chiral aldehydes have received increasing attention in enantioselective catalysis. However, only very few catalytic methods have been developed to construct structurally diverse axially chiral aldehydes. We herein describe an NHC-catalyzed atroposelective esterification of biaryl dialdehydes as a general and practical strategy for the construction of axially chiral aldehydes. Mechanistic studies indicate that coupling proceeds through a novel combination of NHC-catalyzed desymmetrization of the dialdehydes and kinetic resolution. This protocol features excellent enantioselectivity, mild conditions, good functional-group tolerance, and applicability to late-stage functionalization and provides a modular platform for the synthesis of axially chiral aldehydes and their derivatives.
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页数:7
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