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Diastereoselective synthesis of trifluoromethylated 1,3-dioxanes by intramolecular oxa-Michael reaction†
Liliana Becerra-Figueroa,Elodie Brun,Michael Mathieson,Louis J. Farrugia,Claire Wilson,Joëlle Prunet,Diego Gamba-Sánchez
Organic & Biomolecular Chemistry Pub Date : 11/23/2016 00:00:00 , DOI:10.1039/C6OB02333A
Abstract

A highly diastereoselective synthesis of trifluoromethylated 1,3-dioxanes is described. The reaction proceeds by an addition/oxa-Michael sequence and works efficiently under mild reaction conditions, with a good substrate scope and acceptable to good yields.

Graphical abstract: Diastereoselective synthesis of trifluoromethylated 1,3-dioxanes by intramolecular oxa-Michael reaction
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