Asymmetric Organocatalytic Michael Addition of Anthrone to Enone

Overview

Journal Org Biomol Chem

Publisher Royal Society of Chemistry

Specialties Biochemistry
Chemistry

Date 2010 May 25

PMID 20495718

Citations 3

Authors

Chunlin Wu

Wenjun Li

Juanjuan Yang

Xinmiao Liang

Jinxing Ye

Affiliations

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Abstract

Catalyzed by the bifunctional tertiary amino-thiourea organocatalyst derived from epicinchona alkaloid, the asymmetric Michael addition of anthrone to enone was achieved in high yield with excellent enantioselectivity.

Citing Articles

Enantioselective Michael reaction of anthrone catalyzed by chiral tetraoxacalix[2]arene[2]triazine derivatives.

Genc H RSC Adv. 2022; 9(36):21063-21069.

PMID: 35515554 PMC: 9065986. DOI: 10.1039/c9ra03029h.

Effect of Substitution of Hydrogen Atoms in the Molecules of Anthrone and Anthraquinone.

Szymanska M, Majerz I Molecules. 2021; 26(2).

PMID: 33477805 PMC: 7832899. DOI: 10.3390/molecules26020502.

A Diels-Alder Reaction Conducted Within the Parameters of Aqueous Organocatalysis: Still Just Smoke and Mirrors.

Stowe G, Janda K Tetrahedron Lett. 2011; 52(17):2085-2087.

PMID: 21516231 PMC: 3079225. DOI: 10.1016/j.tetlet.2010.10.134.