Issue 31, 2015

Copper-catalyzed trifluoromethylation of alkenes: synthesis of trifluoromethylated benzoxazines

Abstract

A simple base and ligand free copper catalyzed method for the construction of trifluoromethylated benzoxazines has been developed by using Umemoto's reagent. It involves the oxidative difunctionalization of alkenes through tandem C–O and C–CF3 bond formations. Furthermore, synthesized benzoxazines were selectively converted into trifluoromethylated allylic and (E)-vinylic benzamides by the treatment of KOtBu and CH3Li, respectively.

Graphical abstract: Copper-catalyzed trifluoromethylation of alkenes: synthesis of trifluoromethylated benzoxazines

Supplementary files

Article information

Article type
Communication
Submitted
11 Jun 2015
Accepted
02 Jul 2015
First published
03 Jul 2015
This article is Open Access
Creative Commons BY license

Org. Biomol. Chem., 2015,13, 8411-8415

Copper-catalyzed trifluoromethylation of alkenes: synthesis of trifluoromethylated benzoxazines

S. Jana, A. Ashokan, S. Kumar, A. Verma and S. Kumar, Org. Biomol. Chem., 2015, 13, 8411 DOI: 10.1039/C5OB01196E

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