Issue 19, 1979

New syntheses of racemic nuciferal, ar-turmerone, and ipsdienol by a ready regio- and stereo-specific allylic oxidation

Abstract

A simple regio- and stereo-specific terminal and internal allylic oxidation via benzenesulphenyl chloride addition is reported; using this method racemic nuciferal (11) and ar-turmerone (12) were synthesized from racemic α-curcumene (1a), and racemic ipsdienol (10c) from myrcene (1c).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1979, 855-856

New syntheses of racemic nuciferal, ar-turmerone, and ipsdienol by a ready regio- and stereo-specific allylic oxidation

Y. Masaki, K. Hashimoto, K. Sakuma and K. Kaji, J. Chem. Soc., Chem. Commun., 1979, 855 DOI: 10.1039/C39790000855

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