Efficient Decarboxylative/Defluorinative Alkylation for the Synthesis of gem ‐Difluoroalkenes through an S N 2 ’‐Type Route-Reference-Cited by-同舟云学术

Efficient Decarboxylative/Defluorinative Alkylation for the Synthesis of gem ‐Difluoroalkenes through an S N 2 ’‐Type Route

Published:2021-12-19 Issue:3 Volume:40 Page:323-328
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Xing Wei‐Long¹,Wang Jia‐Xin¹,Fu Ming‐Chen¹,Fu Yao¹

Affiliation:

1. Hefei National Laboratory for Physical Sciences at the Microscale, CAS Key Laboratory of Urban Pollutant Conversion, Anhui Province Key Laboratory of Biomass Clean Energy, iChEM, University of Science and Technology of China Hefei Anhui 230026 China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.202100709

Reference60 articles.

1. Organofluorine Chemistry

2. Fluorine and Fluorinated Motifs in the Design and Application of Bioisosteres for Drug Design

3. Nickel-Catalyzed Defluorinative Reductive Cross-Coupling of gem-Difluoroalkenes with Unactivated Secondary and Tertiary Alkyl Halides

4. Copper-Catalyzed Regioselective Monodefluoroborylation of Polyfluoroalkenes en Route to Diverse Fluoroalkenes

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