Issue 23, 1995

Stereo- and enantio-controlled synthesis of (+)-juvabione and (+)-epijuvabione from (+)-norcamphor

Abstract

(+)-Juvabione and (+)-epijuvabione, natural sesquiterpenes exhibiting insect juvenile hormone activity, have been synthesized with complete stereo- and enantio-control using (+)-norcamphor as the chiral precursor via both the enantiomeric bicyclo[3.2.1]octenone intermediates.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 2403-2404

Stereo- and enantio-controlled synthesis of (+)-juvabione and (+)-epijuvabione from (+)-norcamphor

M. Kawamura and K. Ogasawara, J. Chem. Soc., Chem. Commun., 1995, 2403 DOI: 10.1039/C39950002403

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