Formation and Reactions of Perfluoroalkylzinc Compounds Promoted by Ultrasound

5Citations
Citations of this article
1Readers
Mendeley users who have this article in their library.
Get full text

Abstract

A number of “Grignard-type” reactions of organic fluorine compounds were achieved by treating perfluoroalkyl iodides and substrates with zinc under the irradiation of ultrasound. The reactions include 1) Direct carboxylation of perfluoroalkyl iodides, 2) Perfluoroalkylation of carbonyl compounds, 3) Perfluoroalkylation of allyl, vinyl and aryl halides, and 4) Hydroperfluoroalkylation of alkynes and dienes. © 1983, The Society of Synthetic Organic Chemistry, Japan. All rights reserved.

Cite

CITATION STYLE

APA

Ishikawa, N., & Kltazume, T. (1983). Formation and Reactions of Perfluoroalkylzinc Compounds Promoted by Ultrasound. Journal of Synthetic Organic Chemistry, Japan, 41(5), 432–438. https://doi.org/10.5059/yukigoseikyokaishi.41.432

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free