Issue 12, 2005

Lewis acid mediated endo-cyclisation of trimethylsilylmethylenecyclopropyl imines—a stereoselective route to indolizidines

Abstract

Lewis acid mediated endo-cyclisation of trimethylsilylmethylenecyclopropyl imines provides a stereoselective route to indolizidines via a novel cascade sequence.

Graphical abstract: Lewis acid mediated endo-cyclisation of trimethylsilylmethylenecyclopropyl imines—a stereoselective route to indolizidines

Article information

Article type
Communication
Submitted
10 Dec 2004
Accepted
20 Jan 2005
First published
02 Feb 2005

Chem. Commun., 2005, 1637-1639

Lewis acid mediated endo-cyclisation of trimethylsilylmethylenecyclopropyl imines—a stereoselective route to indolizidines

S. Rajamaki and J. D. Kilburn, Chem. Commun., 2005, 1637 DOI: 10.1039/B418476A

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