Chloramphenicol base chemistry. Part 11: 1 chloramphenicol base-derived thiourea-catalyzed enantioselective Michael addition of malononitrile to α , β -unsaturated ketones-Reference-Cited by-同舟云学术

Chloramphenicol base chemistry. Part 11: 1 chloramphenicol base-derived thiourea-catalyzed enantioselective Michael addition of malononitrile to α , β -unsaturated ketones

Published:2017-07 Issue:7 Volume:28 Page:921-929
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Yan Linjie,Wang Haifeng,Xiong Fangjun,Tao Yuan,Wu Yan,Chen Fener

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference71 articles.

1. Chloramphenicol base chemistry. Part 10 1 : Asymmetric synthesis of α -hydroxy chiral alcohols via intramolecular Michael additions of γ -hydroxy- α , β -unsaturated enones with chloramphenicol base derived bifunctional urea organocatalysts

2. Enantioselective Michael Additions to α,β-Unsaturated Imides Catalyzed by a Salen−Al Complex

3. Enantioselective Michael addition reactions of malononitrile catalyzed by chiral Lewis acid and achiral amine catalysts

4. Highly Enantioselective Conjugate Additions to α,β-Unsaturated Ketones Catalyzed by a (Salen)Al Complex

5. Enantioselective Michael Addition to α,β-Unsaturated Imides Catalyzed by a Bifunctional Organocatalyst

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