Issue 0, 1973

Allenes. Part XXVIII. Synthesis of antibiotic lactols and an allenic ester by Claisen rearrangement of prop-2-ynyl vinyl ethers

Abstract

Naturally occurring 4-hydroxy-2-vinylbut-2-en-4-olide (V), an allenic analogue [4-hydroxy-3,3-dimethyl-2-vinylidenebutan-4-olide (VII)], and the corresponding aldehyde ester [ethyl 2-(1-formyl-1-methylethyl)buta-2,3-dienoate (VIII)] have been synthesised by a Claisen-type sigmatropic rearrangement of 3-carboxyprop-2-ynyl vinyl ethers.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1973, 1349-1352

Allenes. Part XXVIII. Synthesis of antibiotic lactols and an allenic ester by Claisen rearrangement of prop-2-ynyl vinyl ethers

D. K. Black, Z. T. Fomum, P. D. Landor and S. R. Landor, J. Chem. Soc., Perkin Trans. 1, 1973, 1349 DOI: 10.1039/P19730001349

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