Enantioselectivity switch in asymmetric Michael addition reactions using phosphonium salts-Reference-Cited by-同舟云学术

Enantioselectivity switch in asymmetric Michael addition reactions using phosphonium salts

Published:2021 Issue:28 Volume:19 Page:6334-6340
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Fang Guosheng¹²³⁴,Wang Hongyu⁵⁶⁷⁸⁹,Zheng Changwu⁵⁶⁷⁸⁹,Pan Lu⁵⁶⁷⁸⁹,Zhao Gang¹²³⁴⁵^ORCID

Affiliation:

1. Department of Chemistry

2. University of Science and Technology of China

3. Hefei 230026

4. China

5. Center for Excellence in Molecular Synthesis

6. Key Laboratory of Synthetic Chemistry of Natural Substances

7. Shanghai Institute of Organic Chemistry

8. Chinese Academy of Sciences

9. Shanghai 200032

Abstract

A catalyst-controlled enantioselectivity switch for asymmetric Michael reactions has been successfully realized by fine tuning chiral organophosphonium salts.

Funder

National Natural Science Foundation of China

Chinese Academy of Sciences

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB01027A

Reference110 articles.

1. Exploring Hydrogen Bond in Biological Molecules

2. Small-Molecule H-Bond Donors in Asymmetric Catalysis

3. Asymmetric Catalysis by Chiral Hydrogen-Bond Donors

4. Design Strategies for Enhanced Hydrogen-Bond Donor Catalysts

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