Next Article in Journal
Previous Article in Journal
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
Received: 24 November 2000; in revised form: 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.

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.

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