Asymmetric Binary Acid Catalysis: Switchable Enantioselectivity in Enantioselective Conjugate Hydride Reduction-Reference-Cited by-同舟云学术

Asymmetric Binary Acid Catalysis: Switchable Enantioselectivity in Enantioselective Conjugate Hydride Reduction

Published:2023-01-10 Issue:2 Volume:25 Page:373-377
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Man¹,Song Ran¹,Yang Daoshan¹,Lv Jian¹^ORCID

Affiliation:

1. Key Laboratory of Optic-electric Sensing and Analytic Chemistry for Life Science, MOE, College of Chemistry and Molecular Engineering, Qingdao University of Science & Technology, Qingdao 266042, China

Funder

Qingdao University of Science and Technology

Taishan Scholar Project of Shandong Province

Natural Science Foundation of Shandong Province

Youth Innovation Science and Technology Plan of Colleges and Universities in Shandong Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c04087

Reference43 articles.

1. aLiu, G.Q.; Li, Y.M.; Chan, A. S. C. Principles and Applications of Asymmetric Synthesis; John Wiley & Sons, Inc.: New York, 2001; pp 1–69.

2. The chiral pool as a source of enantioselective catalysts and auxiliaries

3. Reversal of enantioselectivity in chiral metal complex-catalyzed asymmetric reactions

4. Stereodivergent Catalysis

5. Artificial switchable catalysts

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