Synthesis of Propargylamines via Michael Addition Using Methyl Vinyl Ketone Derivatives, 1-Alkynes, and Secondary Amines Catalyzed by Copper (I) Halides-Reference-Cited by-同舟云学术

Synthesis of Propargylamines via Michael Addition Using Methyl Vinyl Ketone Derivatives, 1-Alkynes, and Secondary Amines Catalyzed by Copper (I) Halides

Published:2019-12-02 Issue:25 Volume:4 Page:21587-21595
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Udaykumar Bantu¹,Periasamy Mariappan¹^ORCID

Affiliation:

1. School of Chemistry, University of Hyderabad Central University P.O., Hyderabad 500046, India

Funder

Council of Scientific and Industrial Research, India

University Grants Commission

Science and Engineering Research Board

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acsomega.9b03428

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2. Highly selective and operationally simple synthesis of enantiomerically pure .beta.-amino esters via double stereodifferentiation

3. Lithium Alkoxides of Cinchona Alkaloids as Chiral Controllers for Enantioselective Acetylide Addition to Cyclic N-Acyl Ketimines

4. An Efficient Chiral Moderator Prepared from Inexpensive (+)-3-Carene: Synthesis of the HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitor DPC 963

5. Preparation of a series of highly hindered secondary amines, including bis(triethylcarbinyl)amine

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