Literature DB >> 20495718

Asymmetric organocatalytic Michael addition of anthrone to enone.

Chunlin Wu1, Wenjun Li, Juanjuan Yang, Xinmiao Liang, Jinxing Ye.   

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.

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Year:  2010        PMID: 20495718     DOI: 10.1039/b927421a

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

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

Authors:  G Neil Stowe; Kim D Janda
Journal:  Tetrahedron Lett       Date:  2011-04-27       Impact factor: 2.415

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

Authors:  Małgorzata Szymańska; Irena Majerz
Journal:  Molecules       Date:  2021-01-19       Impact factor: 4.411

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

Authors:  Hayriye Nevin Genc
Journal:  RSC Adv       Date:  2019-07-05       Impact factor: 4.036

  3 in total

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