Issue 15, 1976

Synthesis of bicyclic α-methylene-γ-lactones involving stereocontrolled introduction of an homoallylic acyloxy group

Abstract

Syntheses of 6-endo-(VI) and 6-exo-acetoxy-4-methylene-2-oxabicyclo[3.3.0]oct-7-en-3-one (XI) from readily available bromolactones (I) and (VII) have been accomplished through formation and dehydrohalogenation of intermediate iodoacetates.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1976, 584-585

Synthesis of bicyclic α-methylene-γ-lactones involving stereocontrolled introduction of an homoallylic acyloxy group

S. M. Ali and S. M. Roberts, J. Chem. Soc., Chem. Commun., 1976, 584 DOI: 10.1039/C39760000584

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