Next Article in Journal
Generation and Cycloaddition of o-Quinodimethane in Aqueous Medium
Previous Article in Journal
Characterisation of Neuropeptide Y Receptor Subtypes by Synthetic NPY Analogues and by Anti-receptor Antibodies
Molecules 2001, 6(5), 468-471; doi:10.3390/60500468
Article

Facile and efficient synthesis of 3β-hydroxy-eupholanost-8-en-24-one

1,* , 1
 and 2
1 Laboratoire de Chimie des Substances Naturelles et des Hétérocycles, Université Cadi Ayyad, Faculté des Sciences Semlalia. BP 2390 Boulevard Prince My Abdellah. Marrakech, Morocco 2 Laboratoire de Chimie de Synthèse et Activations de Biomolécules, Ecole Nationale Supérieure de Chimie de Rennes. Avenue du Général Leclerc 35700 RENNES, France
* Author to whom correspondence should be addressed.
Received: 24 November 2000 / Revised: 20 December 2000 / Accepted: 20 December 2000 / Published: 30 April 2001
Download PDF [24 KB, uploaded 18 June 2014]

Abstract

The epoxidation of the natural product α-euphol followed by cleavage of the obtained epoxide with BF3-etherate, provides 3β-hydroxy-eupholanost-8-en-24-one in satisfactory overall yield.
Keywords: α-euphol; 3β-hydroxy-eupholanost-8-en-24-one; epoxide cleavage α-euphol; 3β-hydroxy-eupholanost-8-en-24-one; epoxide cleavage
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Share & Cite This Article

Export to BibTeX |
EndNote


MDPI and ACS Style

El Aouad, N.; Benharref, A.; Gree, R. Facile and efficient synthesis of 3β-hydroxy-eupholanost-8-en-24-one. Molecules 2001, 6, 468-471.

View more citation formats

Related Articles

Article Metrics

Comments

Citing Articles

[Return to top]
Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert