Issue 21, 2012

Hg(OTf)2-catalyzed direct vinylation of tryptamines and versatile applications for tandem reactions

Abstract

We have developed a unique catalytic protocol for direct gem-vinylation of tryptamine derivatives employing Hg(OTf)2 as the optimum catalyst. The intermolecular vinylations with a series of aromatic acetylenes proceeded under ambient temperature at the C2 positions of indoles with high functional group tolerance. Based on the mechanistic insights, we further developed the tandem reactions successfully constructing a quaternary center.

Graphical abstract: Hg(OTf)2-catalyzed direct vinylation of tryptamines and versatile applications for tandem reactions

Supplementary files

Article information

Article type
Paper
Submitted
01 Feb 2012
Accepted
22 Mar 2012
First published
23 Mar 2012

Org. Biomol. Chem., 2012,10, 4236-4242

Hg(OTf)2-catalyzed direct vinylation of tryptamines and versatile applications for tandem reactions

H. Mizoguchi, H. Oikawa and H. Oguri, Org. Biomol. Chem., 2012, 10, 4236 DOI: 10.1039/C2OB25236H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements