Organocatalytic enantioselective transformations involving quinone derivatives as reaction partners

Xiao Zhang; Ye Hui Chen; Bin Tan

doi:10.1016/j.tetlet.2017.12.055

Organocatalytic enantioselective transformations involving quinone derivatives as reaction partners

Xiao Zhang
, Ye Hui Chen
, Bin Tan^*

^*Corresponding author for this work

School of Chemistry and Chemical Engineering, Harbin Institute of Technology
Southern University of Science and Technology

Research output: Contribution to journal › Review article › peer-review

48 Scopus citations

Abstract

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.

Original language	English
Pages (from-to)	473-486
Number of pages	14
Journal	Tetrahedron Letters
Volume	59
Issue number	6
DOIs	https://doi.org/10.1016/j.tetlet.2017.12.055
State	Published - 7 Feb 2018
Externally published	Yes

Keywords

Arylation
Enantioselective
Michael addition
Organocatalysis
Quinone derivatives

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10.1016/j.tetlet.2017.12.055

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title = "Organocatalytic enantioselective transformations involving quinone derivatives as reaction partners",

abstract = "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.",

keywords = "Arylation, Enantioselective, Michael addition, Organocatalysis, Quinone derivatives",

author = "Xiao Zhang and Chen, \{Ye Hui\} and Bin Tan",

note = "Publisher Copyright: {\textcopyright} 2017 Elsevier Ltd",

year = "2018",

month = feb,

day = "7",

doi = "10.1016/j.tetlet.2017.12.055",

language = "英语",

volume = "59",

pages = "473--486",

journal = "Tetrahedron Letters",

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TY - JOUR

T1 - Organocatalytic enantioselective transformations involving quinone derivatives as reaction partners

AU - Zhang, Xiao

AU - Chen, Ye Hui

AU - Tan, Bin

PY - 2018/2/7

Y1 - 2018/2/7

N2 - 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.

AB - 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.

KW - Arylation

KW - Enantioselective

KW - Michael addition

KW - Organocatalysis

KW - Quinone derivatives

UR - https://www.scopus.com/pages/publications/85039915664

U2 - 10.1016/j.tetlet.2017.12.055

DO - 10.1016/j.tetlet.2017.12.055

M3 - 文献综述

AN - SCOPUS:85039915664

SN - 0040-4039

VL - 59

SP - 473

EP - 486

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 6

ER -

Organocatalytic enantioselective transformations involving quinone derivatives as reaction partners

Abstract

Keywords

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