Issue 14, 2003

Heck arylation of cyclic enol ethers with aryldiazonium salts: regio- and stereoselective synthesis of arylated oxacycles

Abstract

Dihydropyrans and dihydrofurans bearing an aryl substituent in the 2-position are regio- and stereoselectively synthesized by Heck arylation of cyclic enol ethers with aryldiazonium salts.

Graphical abstract: Heck arylation of cyclic enol ethers with aryldiazonium salts: regio- and stereoselective synthesis of arylated oxacycles

Article information

Article type
Communication
Submitted
08 May 2003
Accepted
23 May 2003
First published
05 Jun 2003

Chem. Commun., 2003, 1656-1657

Heck arylation of cyclic enol ethers with aryldiazonium salts: regio- and stereoselective synthesis of arylated oxacycles

B. Schmidt, Chem. Commun., 2003, 1656 DOI: 10.1039/B305142K

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