Issue 5, 2003

First example of electrophile induced Baylis–Hillman reaction: a novel facile one-pot synthesis of indolizine derivatives

Abstract

Treatment of pyridine-2-carboxaldehyde with activated alkenes such as alkyl vinyl ketones and cyclic enones in the presence of trimethylsilyl trifluoromethanesulfonate (TMSOTf) provides a novel facile one-pot synthesis of indolizine derivatives, thus for the first time describing an electrophile induced Baylis–Hillman reaction.

Graphical abstract: First example of electrophile induced Baylis–Hillman reaction: a novel facile one-pot synthesis of indolizine derivatives

Supplementary files

Article information

Article type
Communication
Submitted
19 Nov 2002
Accepted
13 Jan 2003
First published
17 Feb 2003

Chem. Commun., 2003, 604-605

First example of electrophile induced Baylis–Hillman reaction: a novel facile one-pot synthesis of indolizine derivatives

D. Basavaiah and A. Jaganmohan Rao, Chem. Commun., 2003, 604 DOI: 10.1039/B211349J

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