Next Article in Journal
Shelf-Life of an Extruded Blend of Peanut, Soybean and Corn
Previous Article in Journal
Chemical Modifications of 1,2,5-Oxadiazole N-Oxide System Searching for Cytotoxic Selective Hypoxic Drugs
Article Menu

Export Article

Open AccessAbstract
Molecules 2000, 5(3), 522-523; https://doi.org/10.3390/50300522

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

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
View Full-Text   |   Download PDF [17 KB, uploaded 18 June 2014]

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. View Full-Text
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).
SciFeed

Share & 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.

Show more citation formats Show less citations formats

Related Articles

Article Metrics

Article Access Statistics

1

Comments

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