Highly efficient asymmetric organocatalytic Michael addition of α,α-disubstituted aldehydes to nitroolefins under solvent-free conditions-Reference-Cited by-同舟云学术

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Highly efficient asymmetric organocatalytic Michael addition of α,α-disubstituted aldehydes to nitroolefins under solvent-free conditions

Published:2014-05 Issue:19 Volume:55 Page:3030-3032
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

He Junpeng,Chen Qiankun,Ni Bukuo

Funder

College of Science, Engineering & Agriculture

Texas A&M University-Commerce

National Science Foundation

McNair Scholars Program

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference72 articles.

1. Recent Advances in Asymmetric Organocatalytic Construction of 3,3′-Spirocyclic Oxindoles

2. Evolution of asymmetric organocatalysis: multi- and retrocatalysis

3. Low-loading asymmetric organocatalysis

4. Recent Developments in Asymmetric Organocatalytic Domino Reactions

5. Organocatalytic Formation of Quaternary Stereocenters

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Greener Approaches to Selected Asymmetric Addition Reactions Relevant to Drug Development;Current Organic Chemistry;2021-09-02

2. Asymmetric Michael Addition of Isobutyraldehyde to Nitroolefins Using an α,α-Diphenyl-(S)-prolinol-Derived Chiral Diamine Catalyst;Bulletin of the Chemical Society of Japan;2020-08-15

3. Innovative catalysis in Michael addition reactions for C-X bond formation;Molecular Catalysis;2020-04

4. Recent Advances in Solvent‐Free Asymmetric Catalysis;ChemCatChem;2019-05-27

5. Addition Reactions: Polar Addition;Organic Reaction Mechanisms · 2014;2018-01-05

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