Creation of a Chiral All-Carbon Quaternary Center Induced by CF<sub>3</sub> and CH<sub>3</sub> Substituents via Cu-Catalyzed Asymmetric Conjugate Addition-Reference-Cited by-同舟云学术

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Creation of a Chiral All-Carbon Quaternary Center Induced by CF₃ and CH₃ Substituents via Cu-Catalyzed Asymmetric Conjugate Addition

Published:2024-06-13 Issue:25 Volume:26 Page:5312-5317
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Yamamoto Taiyo¹,Asakura Masayuki¹,Yamanomoto Ken¹^ORCID,Shibata Takanori²^ORCID,Endo Kohei¹^ORCID

Affiliation:

1. Department of Chemistry, Faculty of Science, Tokyo University of Science, Shinjuku, Tokyo 162-8601, Japan

2. Department of Chemistry and Biochemistry, Graduate School of Science and Technology, Waseda University, Shinjuku, Tokyo 169-8555, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c01691

Reference66 articles.

1. Approaches to Obtaining Fluorinated α-Amino Acids

2. Modern Approaches for Asymmetric Construction of Carbon–Fluorine Quaternary Stereogenic Centers: Synthetic Challenges and Pharmaceutical Needs

3. Monofluorination of Organic Compounds: 10 Years of Innovation

4. Advances in Catalytic Enantioselective Fluorination, Mono-, Di-, and Trifluoromethylation, and Trifluoromethylthiolation Reactions

5. Update 1 of: Asymmetric Fluorination, Trifluoromethylation, and Perfluoroalkylation Reactions

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