Issue 3, 1993

A radical cyclisation strategy to α-spiro-β-methylene-γ-butyrolactones. Total synthesis of (±)-norbakkenolide-A

Abstract

The 5-exo-dig radical cyclisation reaction of the bromoacetals 9, obtained from the enol ethers 8, and treatment of the resulting hemiacetal 10 with Jones′ reagent transforms the cyclic ketones 7 and 12 into α-spiro-β-methylene-γ-butyrolactones 11 and norbakkenolide-A 2.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 285-288

A radical cyclisation strategy to α-spiro-β-methylene-γ-butyrolactones. Total synthesis of (±)-norbakkenolide-A

A. Srikrishna, S. Nagaraju and G. V. R. Sharma, J. Chem. Soc., Chem. Commun., 1993, 285 DOI: 10.1039/C39930000285

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