Cinchona Alkaloid‐Derived Zwitterions Catalyzed Enantioselective Steglich Rearrangement and Aldol Reaction of <i>O</i> ‐Acylated Oxindoles-Reference-Cited by-同舟云学术

Cinchona Alkaloid‐Derived Zwitterions Catalyzed Enantioselective Steglich Rearrangement and Aldol Reaction of O ‐Acylated Oxindoles

Published:2022-02-17 Issue:8 Volume:14 Page:
ISSN:1867-3880
Container-title:ChemCatChem
language:en
Short-container-title:ChemCatChem

Author:

Lam Ying‐Pong¹,Huang Jingxian¹,Jiang Xiaojian²^ORCID,Yeung Ying‐Yeung¹^ORCID

Affiliation:

1. Department of Chemistry and State Key Laboratory of Synthetic Chemistry The Chinese University of Hong Kong Shatin N.T., Hong Kong P. R. China

2. International Cooperative Laboratory of Traditional Chinese Medicine Modernization and Innovative Drug Development of Chinese Ministry of Education Collage of Pharmacy Jinan University Guangzhou 510632 P. R. China

Funder

Innovation and Technology Commission

Publisher

Wiley

Subject

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

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cctc.202200136

Reference53 articles.

1. Cooperative Catalysis Involving Chiral Ion Pair Catalysts

2. Asymmetric Organic Catalysis with Modified Cinchona Alkaloids

3. Bifunctional Amine-Squaramides: Powerful Hydrogen-Bonding Organocatalysts for Asymmetric Domino/Cascade Reactions

4. Amide-based bifunctional organocatalysts in asymmetric reactions

5. Asymmetric organocatalytic reactions by bifunctional amine-thioureas

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