Issue 11, 1985

A stereoselective total synthesis of (±)-dihydrosecologanin aglucone

Abstract

Racemic dihydrosecologanin aglucone (2) has been prepared via substituted cyclopentenolones in an efficient synthetic sequence involving a novel selective decarboalkoxylation of β-keto-esters as a key step.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 699-700

A stereoselective total synthesis of (±)-dihydrosecologanin aglucone

R. T. Brown and M. F. Jones, J. Chem. Soc., Chem. Commun., 1985, 699 DOI: 10.1039/C39850000699

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