Organocatalytic Enantioconvergent Synthesis of Tetrasubstituted Allenes via Asymmetric 1,8-Addition to aza-para-Quinone Methides

被引:72
|
作者
Chen, Min [1 ,2 ]
Qian, Deyun [1 ,2 ]
Sun, Jianwei [1 ,2 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Chem, Kowloon, Clear Water Bay, Hong Kong, Peoples R China
[2] Hong Kong Univ Sci & Technol, Shenzhen Res Inst, Kowloon, Clear Water Bay, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
BRONSTED ACID; 1,6-CONJUGATE ADDITION; ENANTIOSELECTIVE SYNTHESIS; CYCLOADDITIONS; CONSTRUCTION; ACTIVATION; ALKYLATION; POLYMERS; ALCOHOLS; ENAMIDES;
D O I
10.1021/acs.orglett.9b03224
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In contrast to the well-explored quinone methides (QMs) and aza-ortho-QMs, aza-para-QMs have been rarely studied in terms of their asymmetric transformations. Herein, a highly efficient enantioconvergent asymmetric 1,8-addition of aza-para-QMs is described. Featuring remarkable remote stereocontrol, this reaction provides expedient access to chiral tetrasubstituted allenes bearing an adjacent all-carbon quaternary stereocenter with high enantioselectivity and diastereoselectivity.
引用
收藏
页码:8127 / 8131
页数:5
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