Issue 11, 1970

A new synthesis of 2,2-dimethylchromenoquinolines from epoxides: synthesis of the alkaloid flindersine

Abstract

Treatment of isopentenylquinoline epoxides with sodium hydroxide in dimethyl sulphoxide gave chromenoquinolines via allylic alcohol intermediates; this led to a new synthesis of the alkaloid, flindersine.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 666-667

A new synthesis of 2,2-dimethylchromenoquinolines from epoxides: synthesis of the alkaloid flindersine

R. M. Bowman, M. F. Grundon and K. J. James, J. Chem. Soc. D, 1970, 666 DOI: 10.1039/C29700000666

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