Approach to the A-B Ring System of Forskolin through Biotransformation of Toluene

doi:10.3390/50300522

This article is

freely available
re-usable

Molecules 2000, 5(3), 522-523; doi:10.3390/50300522

Article

Approach to the A-B Ring System of Forskolin through Biotransformation of Toluene

V. Schapiro* , G. Seoane and G. García

Cátedra de Química Orgánica, Facultad de Química, Gral. Flores 2124, Universidad de la República, Montevideo, Uruguay

* Author to whom correspondence should be addressed.

Published: 22 March 2000

Download PDF Full-Text [17 KB, uploaded 24 November 2008 11:42 CET]

Abstract: In the present work, we will intend to show that diol I, microbially derived from toluene using Pseudomonas putida 39D, is a suitable synthon for the synthesis of the A-B ring system of forskolin. The functionalization of diol I, to be used as ring-B, and the attempts of ring-A closure, will be disclosed.

Article Statistics

Click here to load and display the download statistics.

Cite This Article

MDPI and ACS Style

Schapiro, V.; Seoane, G.; García, G. Approach to the A-B Ring System of Forskolin through Biotransformation of Toluene. Molecules 2000, 5, 522-523.

AMA Style

Schapiro V, Seoane G, García G. Approach to the A-B Ring System of Forskolin through Biotransformation of Toluene. Molecules. 2000; 5(3):522-523.

Chicago/Turabian Style

Schapiro, V.; Seoane, G.; García, G. 2000. "Approach to the A-B Ring System of Forskolin through Biotransformation of Toluene." Molecules 5, no. 3: 522-523.

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