Catalyst-Controlled Diastereoselectivity Switch in the Asymmetric [3 + 2] Annulation of Isatin-Derived MBH Carbonates and 5-Alkenylthiazol-4(5H)-ones-Reference-Cited by-同舟云学术

Catalyst-Controlled Diastereoselectivity Switch in the Asymmetric [3 + 2] Annulation of Isatin-Derived MBH Carbonates and 5-Alkenylthiazol-4(5H)-ones

Published:2021-09-15 Issue:19 Volume:23 Page:7336-7341
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Mei Ming-Shun¹²,Wang Ya-Jie²,Zhang Gui-Shan²,Tang Jing-Yi¹,Tian Ping²^ORCID,Wang Yu-Hui²^ORCID

Affiliation:

1. Department of Cardiovascular Research Laboratory, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200032, China

2. Shanghai Frontiers Science Center for Traditional Chinese Medicine Chemical Biology, Innovation Research Institute of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, 1200 Cailun Road, Shanghai 201203, China

Funder

Shanghai Municipal Education Commission

Science and Technology Commission of Shanghai Municipality

National Natural Science Foundation of China

Program of Shanghai Academic/Technology Research Leader

National Administration of Traditional Chinese Medicine

Chenguang Program

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c02421

Reference27 articles.

1. Catalytic Strategies for Diastereodivergent Synthesis

2. Stereodivergent Catalysis

3. Advances in Asymmetric Diastereodivergent Catalysis

4. Switchable divergent asymmetric synthesis via organocatalysis

5. Transformations of Modified Morita‐Baylis‐Hillman Adducts from Isatins Catalyzed by Lewis Bases

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