Issue 47, 2009
From the journal:

Chemical Communications

Stereoselective gold-catalyzed cycloaddition of functionalized ketoenynes: synthesis of (+)-orientalol F†‡

Eloísa Jiménez-Núñez,a   Kian Molawia  and  Antonio M. Echavarren*ab  

* Corresponding authors

a Institute of Chemical Research of Catalonia (ICIQ), Av. Països Catalans 16, 43007 Tarragona, Spain
E-mail: aechavarren@iciq.es

b Departament de Química Analítica i Química Orgànica, Universitat Rovira i Virgili, C/Marcelli Domingo s/n, 43007 Tarragona, Spain

Abstract

A stereoselective gold-catalyzed [2 + 2 + 2] cycloaddition of ketoenynes substituted at the propargylic position with OR groups has been applied for the synthesis of (+)-orientalol F and pubinernoid B.

Graphical abstract: Stereoselective gold-catalyzed cycloaddition of functionalized ketoenynes: synthesis of (+)-orientalol F

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B920119J
Article type
Communication
Submitted
28 Қыр. 2009
Accepted
19 Қаз. 2009
First published
05 Қар. 2009

Chem. Commun., 2009, 7327-7329

Permissions

Request permissions

Stereoselective gold-catalyzed cycloaddition of functionalized ketoenynes: synthesis of (+)-orientalol F

E. Jiménez-Núñez, K. Molawi and A. M. Echavarren, Chem. Commun., 2009, 7327 DOI: 10.1039/B920119J

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.

Social activity

Spotlight

Advertisements