Issue 15, 1993

An isoxazole route to unsaturated α-alkoxycarbonyl-β-diketones

Abstract

Cycloaddition of diethylphosphonomethyl nitrile oxide to the enamine from ethyl acetoacetate produces 4-ethoxycarbonyl-3-diethoxyphosphonylmethyl-5-methylisoxazole; condensation of the phosphonate with aldehydes and ketones gives 3-alkenylisoxazoles that are cleaved by hexacarbonylmolybdenum to afford unsaturated α-alkoxycarbonyl-β-diketones.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1993, 1715-1716

An isoxazole route to unsaturated α-alkoxycarbonyl-β-diketones

R. C. F. Jones, G. Bhalay and P. A. Carter, J. Chem. Soc., Perkin Trans. 1, 1993, 1715 DOI: 10.1039/P19930001715

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