Issue 96, 2015

Palladium catalyzed C(sp2)–C(sp2) bond formation. A highly regio- and chemoselective oxidative Heck C-3 alkenylation of pyrones and pyridones

Abstract

Palladium catalysed ligand free direct dehydrogenative C-3 alkenylation of pyrones and unprotected pyridones from unactivated alkenes is reported. The process is highly regio- and chemoselective. A wide variety of alkene partners reacted to broaden the substrate scope of the process. The effect of the C-3 substituent on the rate of reaction is also studied.

Graphical abstract: Palladium catalyzed C(sp2)–C(sp2) bond formation. A highly regio- and chemoselective oxidative Heck C-3 alkenylation of pyrones and pyridones

Supplementary files

Article information

Article type
Communication
Submitted
30 Jun 2015
Accepted
10 Sep 2015
First published
10 Sep 2015

RSC Adv., 2015,5, 78958-78961

Author version available

Palladium catalyzed C(sp2)–C(sp2) bond formation. A highly regio- and chemoselective oxidative Heck C-3 alkenylation of pyrones and pyridones

H. U. Lah, F. Rasool and S. K. Yousuf, RSC Adv., 2015, 5, 78958 DOI: 10.1039/C5RA12631B

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