Issue 77, 2015

Metal-free carbonyl C(sp2)–H oxidative alkynylation of aldehydes using hypervalent iodine reagents leading to ynones

Abstract

A new metal-free tert-butyl hydroperoxide (TBHP)-mediated carbonyl C(sp2)–H oxidative alkynylation of aldehydes with ethynyl benziodoxolones (EBX) for the synthesis of ynones is described. This method is based on a carbonyl C(sp2)–H oxidative radical coupling process according to mechanistic studies, and provides a general route to the assembly of diverse ynones with a broad substrate scope and excellent functional-group compatibility.

Graphical abstract: Metal-free carbonyl C(sp2)–H oxidative alkynylation of aldehydes using hypervalent iodine reagents leading to ynones

Supplementary files

Article information

Article type
Communication
Submitted
23 Apr 2015
Accepted
07 Aug 2015
First published
07 Aug 2015

Chem. Commun., 2015,51, 14497-14500

Metal-free carbonyl C(sp2)–H oxidative alkynylation of aldehydes using hypervalent iodine reagents leading to ynones

X. Ouyang, R. Song, C. Wang, Y. Yang and J. Li, Chem. Commun., 2015, 51, 14497 DOI: 10.1039/C5CC03362D

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