Issue 9, 1996

Three-carbon ring-enlargement of ethereal oxonium ylides—a viable synthesis of medium-sized cyclic ketoethers

Abstract

eight- to eleven-membered cyclic ketoethers are synthesized in a single-step by rhodium(II)-catalysed three-carbon ring-enlargement of diazoacetonyl-substituted cyclic ethers via bicyclic ethereal oxonium ylide intermediates.

Article information

Article type
Paper

Chem. Commun., 1996, 1077-1078

Three-carbon ring-enlargement of ethereal oxonium ylides—a viable synthesis of medium-sized cyclic ketoethers

A. Oku, S. Ohki, T. Yoshida and K. Kimura, Chem. Commun., 1996, 1077 DOI: 10.1039/CC9960001077

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