Issue 6, 1995

A new catalytic transformation of diazo esters: hydride abstraction in dirhodium(II)-catalysed reactions

Abstract

Secondary benzylic and allylic diazoacetates undergo dirhodium(II)-catalysed diazo decomposition to form, competitively or exclusively, ketone and vinylidene products from intramolecular hydride abstraction in catalyst ligand-dependent molar ratios.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1995, 619-621

A new catalytic transformation of diazo esters: hydride abstraction in dirhodium(II)-catalysed reactions

M. P. Doyle, A. B. Dyatkin and C. L. Autry, J. Chem. Soc., Perkin Trans. 1, 1995, 619 DOI: 10.1039/P19950000619

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.

Spotlight

Advertisements