Switchable Enantioselectivity in Conjugate Alkyne Addition of β,γ-Unsaturated α-Keto Esters by Asymmetric Binary Acid Catalysis-Reference-Cited by-同舟云学术

Switchable Enantioselectivity in Conjugate Alkyne Addition of β,γ-Unsaturated α-Keto Esters by Asymmetric Binary Acid Catalysis

Published:2024-04-24 Issue:17 Volume:26 Page:3612-3616
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Duan Depeng¹,Tang Mengdie¹,Wang Man¹,Qiu Huixin¹,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

Department of Education of Shandong Province

Qingdao University of Science and Technology

Taishan Scholar Project of Shandong Province

Natural Science Foundation of Shandong Province

Science Fund for Distinguished Young Scholars of Shandong Province

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c01101

Reference34 articles.

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

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

3. Stereodivergent Catalysis

4. Artificial switchable catalysts

5. Chiral Brønsted Acid-Catalyzed Direct Mannich Reactions via Electrophilic Activation

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