Issue 22, 1991

A short, diastereospecific approach to symmetrical and unsymmetrical 2,6-diaryl-3,7-dioxabicyclo[3.3.0]octane lignans

Abstract

Enolate Claisen rearrangement of the lactone 7 leads to the tetrahydrofuran (THF) ester 9 as a single diastereoisomer, reduction of which gives the general bis-THF lignan precursor 2.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 1641-1643

A short, diastereospecific approach to symmetrical and unsymmetrical 2,6-diaryl-3,7-dioxabicyclo[3.3.0]octane lignans

H. M. Bradley and D. W. Knight, J. Chem. Soc., Chem. Commun., 1991, 1641 DOI: 10.1039/C39910001641

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