Carbofluorination of π‐Bonds and Related Reactions Involving Tandem C−C/C−F Bond Formation

Author:

McKnight E. Ali1,Cadwallader Dusty1,Le Christine M.1

Affiliation:

1. Department of Chemistry York University 4700 Keele St Toronto, ON M3J 1P3 Canada

Abstract

AbstractDue to the unique properties of C−F bonds, organofluorine compounds occupy a privileged space in the pharmaceutical, agrochemical, and polymer industries. Carbofluorination reactions involve the formation of a C−C and a C−F bond, typically across a π‐bond or another unsaturated functionality that is revealed upon in situ activation. The design of tailored substrates and new catalyst systems has enabled carbofluorination chemistry to emerge as a promising manifold for the synthesis of unique fluorinated scaffolds. This review covers the application of nucleophilic and electrophilic fluorinating reagents in this chemistry, in addition to recently developed atom‐economical carbofluorination reactions using organofluorine compounds as dual reagents.

Funder

Natural Sciences and Engineering Research Council of Canada

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. BF3-Catalyzed Intramolecular Fluorocarbamoylation of Alkynes via Halide Recycling;Journal of the American Chemical Society;2023-05-12

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