Self-assembled proline-amino thioureas as efficient organocatalysts for the asymmetric Michael addition of aldehydes to nitroolefins-Reference-Cited by-同舟云学术

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Self-assembled proline-amino thioureas as efficient organocatalysts for the asymmetric Michael addition of aldehydes to nitroolefins

Published:2010-12 Issue:24 Volume:21 Page:2925-2933
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Wang Wan-Hui,Abe Takeshi,Wang Xiang-Bo,Kodama Koichi,Hirose Takuji,Zhang Guang-You

Publisher

Elsevier BV

Subject

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

Reference58 articles.

1. Proline-Catalyzed Direct Asymmetric Aldol Reactions

2. In the Golden Age of Organocatalysis

3. Asymmetric organocatalysis

4. Enantioselective organocatalysis

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1. Dipeptidic Proline‐Derived Thiourea Organocatalysts for Asymmetric Michael addition Reactions between Aldehydes and Nitroolefins;ChemistrySelect;2024-08-23

2. Development of Low‐Molecular‐Weight Organogelators from Cyclic β‐Amino Acid: Effect of Stereochemistry and their Application on Visual Chiral Recognition of Amines;Chemistry – A European Journal;2023-01-23

3. Asymmetric Assemblies of 1,3-Dienes, Sulfuric Diamide, and Aldehydes to Access 1,3-Diamines through Relay Amine/Palladium Catalysis;Organic Letters;2022-12-07

4. Synthesis and Catalytic Activity of Organocatalysts Based on Enaminone and Benzenediamine Hydrogen Bond Donors;Catalysts;2022-09-28

5. Chiral 1,3-aminosquaramides derived from cis-2-benzamidocyclohexanecarboxylic acid as organocatalysts for asymmetric Michael addition reactions;Tetrahedron;2022-04

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