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Highly enantioselective iron(ii)-catalyzed opening reaction of aromatic meso-epoxides with indoles†
Baptiste Plancq,Mathieu Lafantaisie,Simon Companys,Cendrella Maroun,Thierry Ollevier
Organic & Biomolecular Chemistry Pub Date : 09/26/2013 00:00:00 , DOI:10.1039/C3OB41782D
Abstract

A highly enantioselective method for the catalytic cis-stilbene oxide opening reaction with indole derivatives was developed. The scope of the reaction was studied with a selection of aromatic meso-epoxides and various indoles, and the desired 2-(indol-3-yl)ethanol derivatives were obtained in good to excellent yields with excellent enantioselectivities (from 96 to >99% ee).

Graphical abstract: Highly enantioselective iron(ii)-catalyzed opening reaction of aromatic meso-epoxides with indoles
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