Molecules 2001, 6(5), 468-471; doi:10.3390/60500468
Article

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

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; in revised form: 20 December 2000 / Accepted: 20 December 2000 / Published: 30 April 2001
PDF Full-text Download PDF Full-Text [24 KB, uploaded 6 October 2008 08:41 CEST]
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

Article Statistics

Load and display the download statistics.

Citations to this Article

Cite This Article

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.

AMA Style

El Aouad N, Benharref A, Gree R. Facile and efficient synthesis of 3β-hydroxy-eupholanost-8-en-24-one. Molecules. 2001; 6(5):468-471.

Chicago/Turabian Style

El Aouad, N.; Benharref, A.; Gree, R. 2001. "Facile and efficient synthesis of 3β-hydroxy-eupholanost-8-en-24-one." Molecules 6, no. 5: 468-471.

Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert