Highly stereoselective metal-free oxyaminations using chiral hypervalent iodine reagents

Angew Chem Int Ed Engl. 2012 Apr 2;51(14):3462-5. doi: 10.1002/anie.201107703. Epub 2012 Jan 25.

Abstract

The ring and I: hypervalent iodine compounds avoid the issues of toxicity or complicated ligands of many transition-metal-based systems. A highly enantioselective oxyamination of alkenes with N-sulfonyl ureas employing chiral, lactic acid-based hypervalent iodine reagents gives a facile synthesis of enantiomerically pure 2-arylproline derivatives for the first time.