Bifunctional Cinchona Alkaloid Catalyzed Vinylogous Michael Reaction of 3–Alkylideneoxindole with 4‐Oxo‐enoates: A Route to Chiral γ‐Keto Alkylideneoxindole Esters-Reference-Cited by-同舟云学术

Bifunctional Cinchona Alkaloid Catalyzed Vinylogous Michael Reaction of 3–Alkylideneoxindole with 4‐Oxo‐enoates: A Route to Chiral γ‐Keto Alkylideneoxindole Esters

Published:2020-09-02 Issue:10 Volume:9 Page:1576-1580
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J. Org. Chem.

Author:

Kumar Rajesh¹,Jaiswal Manish K.¹,Singh Ravi P.¹^ORCID

Affiliation:

1. Department of Chemistry Indian Institute of Technology-Delhi Hauz Khas New Delhi Delhi 110016 India

Funder

Department of Atomic Energy, Government of India

Publisher

Wiley

Subject

Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajoc.202000227

Reference87 articles.

1. For general reviews see:

2. Recent Progress in Asymmetric Bifunctional Catalysis Using Multimetallic Systems

3. Direct, Highly Enantioselective Pyrrolidine Sulfonamide Catalyzed Michael Addition of Aldehydes to Nitrostyrenes

4. Direct, Highly Enantioselective Pyrrolidine Sulfonamide Catalyzed Michael Addition of Aldehydes to Nitrostyrenes

5. Design of Acid−Base Catalysis for the Asymmetric Direct Aldol Reaction

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