Rh-Catalyzed Asymmetric Hydrogenation of 2-Substituted 4<i>H</i>-(Thio)chromenes for Synthesis of Chiral (Thio)chromanes-Reference-Cited by-同舟云学术

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Rh-Catalyzed Asymmetric Hydrogenation of 2-Substituted 4H-(Thio)chromenes for Synthesis of Chiral (Thio)chromanes

Published:2024-07-03 Issue:28 Volume:26 Page:5917-5922
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wu Xiaoxue¹,Li Meina¹,Guo Qianling¹,Zi Guofu¹^ORCID,Hou Guohua¹^ORCID

Affiliation:

1. Key Laboratory of Radiopharmaceuticals, College of Chemistry, Beijing Normal University, Beijing 100875, China

Funder

Beijing Municipal Natural Science Foundation

National Natural Science Foundation of China

Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c01808

Reference58 articles.

1. Studies on a New 1, 5-Benzothiazepine Derivative (CRD-401). IV. Coronary Vasodilating Effect and Structure-Activity Relationship

2. An efficient synthesis of LTD4 antagonist L-699,392

3. Organocatalytic asymmetric domino sulfa-Michael–aldol reactions of 2-mercaptobenzaldehyde with α,β-unsaturated N-acylpyrazoles for the construction of thiochromane

4. Expeditious diastereoselective construction of a thiochroman skeleton via a cinchona alkaloid-derived catalyst

5. Synthesis of Optically Active 2H-Thiopyrano[2,3-b]quinolines with Three Contiguous Stereocentersviaan Organocatalytic Asymmetric Tandem Michael-Henry Reaction

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