Organocatalytic enantioselective transformations involving quinone derivatives as reaction partners

被引：47

作者：

Zhang, Xiao ^{[1
,2
]}

Chen, Ye-Hui ^{[2
]}

Tan, Bin ^{[2
]}

机构：

[1] Harbin Inst Technol, Sch Chem & Chem Engn, Harbin 150080, Heilongjiang, Peoples R China

[2] South Univ Sci & Technol China, Dept Chem, Shenzhen 518055, Peoples R China

来源：

TETRAHEDRON LETTERS | 2018年 / 59卷 / 06期

基金：

中国国家自然科学基金;

关键词：

Quinone derivatives; Organocatalysis; Enantioselective; Michael addition; Arylation; CATALYZED ASYMMETRIC-SYNTHESIS; CHIRAL DICARBOXYLIC-ACID; DIELS-ALDER REACTIONS; MICHAEL ADDITION; BRONSTED ACID; IMINE KETALS; 3-SUBSTITUTED OXINDOLES; CASCADE REACTIONS; ALPHA-ARYLATION; PHOSPHORIC-ACID;

D O I：

10.1016/j.tetlet.2017.12.055

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

This digest summarizes the recent progress made in the organocatalytic asymmetric reactions involving 1,4-quinone derivatives. The roles of quinones as Michael donors, Michael acceptors, dienophiles, 1,3-dipolarophiles and cascade reaction partners have been extensively investigated to access complex structural frameworks in the presence of chiral amine catalysts, phosphoric acid catalysts, bifunctional catalysts (Cinchona alkaloids- and thiourea-based), carboxylic acid catalysts, boronic acid catalysts and cationic oxazaborolidinium ions. (C) 2017 Elsevier Ltd. All rights reserved.

引用

页码：473 / 486

页数：14

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