Palladium-Catalyzed Stereoselective C−F Bond Vinylation and Allylation of Tetrasubstituted gem-Difluoroalkenes via Stille Coupling: Synthesis of Monofluorinated 1,3- and 1,4-Dienes-Reference-Cited by-同舟云学术

Palladium-Catalyzed Stereoselective C−F Bond Vinylation and Allylation of Tetrasubstituted gem-Difluoroalkenes via Stille Coupling: Synthesis of Monofluorinated 1,3- and 1,4-Dienes

Published:2021-09-29 Issue:20 Volume:23 Page:8072-8076
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Li Min¹,Wang Yanhui¹,Tsui Gavin Chit¹^ORCID

Affiliation:

1. Department of Chemistry, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong SAR 999077, China

Funder

Research Grants Council, University Grants Committee

Chinese University of Hong Kong

Key Laboratory of Organofluorine Chemistry

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c03096

Reference25 articles.

1. Transition-Metal-Mediated and -Catalyzed C−F Bond Activation by Fluorine Elimination

2. Recent advances in the synthesis and CF functionalization of gem-difluoroalkenes

3. C−F Bond Activation in Organic Synthesis

4. Synthesis of Monofluoroalkenes: A Leap Forward

5. Synthetic Methods for Fluorinated Olefins

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