Issue 91, 2020

Visible light promoted deaminative difluoroalkylation of aliphatic amines with difluoroenoxysilanes

Abstract

A visible light promoted deaminative strategy for the difluoroalkylation reaction utilizing pyridinium-activated aliphatic primary amines and difluoroenoxysilane as substrates has been developed. This protocol is characteriazed by its mild reaction conditions and broad substrate scope, which converted a diverse array of amine-containing molecules to the alkyl-CF2COPh products. Moreover, the resulting products can be easily transformed into a vast array of structurally novel and interesting difluoro-containing moieties, therefore providing a facile route for applications in medicinal chemistry and the life sciences.

Graphical abstract: Visible light promoted deaminative difluoroalkylation of aliphatic amines with difluoroenoxysilanes

Supplementary files

Article information

Article type
Communication
Submitted
23 Aug 2020
Accepted
19 Oct 2020
First published
20 Oct 2020

Chem. Commun., 2020,56, 14247-14250

Visible light promoted deaminative difluoroalkylation of aliphatic amines with difluoroenoxysilanes

Y. Huang, J. Jia, Q. Huang, L. Zhao, P. Wang, J. Gu and C. He, Chem. Commun., 2020, 56, 14247 DOI: 10.1039/D0CC05725H

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