Issue 21, 2015

Rhenium-catalyzed dehydrogenative olefination of C(sp3)–H bonds with hypervalent iodine(iii) reagents

Abstract

A dehydrogenative olefination of C(sp3)–H bonds is disclosed here, by merging rhenium catalysis with an alanine-derived hypervalent iodine(III) reagent. Thus, cyclic and acyclic ethers, toluene derivatives, cycloalkanes, and nitriles are all successfully alkenylated in a regio- and stereoselective manner.

Graphical abstract: Rhenium-catalyzed dehydrogenative olefination of C(sp3)–H bonds with hypervalent iodine(iii) reagents

Supplementary files

Article information

Article type
Communication
Submitted
30 Mar 2015
Accepted
18 Apr 2015
First published
20 Apr 2015

Org. Biomol. Chem., 2015,13, 5880-5884

Rhenium-catalyzed dehydrogenative olefination of C(sp3)–H bonds with hypervalent iodine(III) reagents

H. Gu and C. Wang, Org. Biomol. Chem., 2015, 13, 5880 DOI: 10.1039/C5OB00619H

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