Organocatalytic enantioselective transformations involving quinone derivatives as reaction partners

Zhang, Xiao1,2; Chen, Ye-Hui2; Tan, Bin2

2018-02-07

10.1016/j.tetlet.2017.12.055

TETRAHEDRON LETTERS   影响因子和分区

0040-4039

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.

Quinone derivatives Organocatalysis Enantioselective Michael addition Arylation

SCI

英语

通讯

South University of Science and Technology of China[FRG-SUSTC1501A-16]

Chemistry

Chemistry, Organic

WOS:000424853400001

PERGAMON-ELSEVIER SCIENCE LTD

CHEMISTRY

Web of Science

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

Zhang, Xiao,Chen, Ye-Hui,Tan, Bin. Organocatalytic enantioselective transformations involving quinone derivatives as reaction partners[J]. TETRAHEDRON LETTERS,2018,59(6):473-486.

Zhang, Xiao,Chen, Ye-Hui,&Tan, Bin.(2018).Organocatalytic enantioselective transformations involving quinone derivatives as reaction partners.TETRAHEDRON LETTERS,59(6),473-486.

Zhang, Xiao,et al."Organocatalytic enantioselective transformations involving quinone derivatives as reaction partners".TETRAHEDRON LETTERS 59.6(2018):473-486.