Events7th International Electronic Conference on Medicinal Chemistry
Published
This submission belongs to the session S3. General of the event 7th International Electronic Conference on Medicinal Chemistry
Published date
03 Nov, 2021
Academic Editor
author-avatarJean Jacques Vanden Eynde
Citation
Inês Martins, Jaime Coelho, Carlos Afonso, Electrochemical oxidation of abietanes, in Proceedings of 7th International Electronic Conference on Medicinal Chemistry, 1 November–30 November 2021, MDPI: Basel, Switzerland, doi: 10.3390/ECMC2021-11549
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Electrochemical oxidation of abietanes

1. Faculty of Pharmacy, University of Lisbon, Portugal
2. Faculty of Sciences of the University of Lisbon
3. Faculty of Pharmacy, University of Lisbon
Abstract

Colophony, a natural resin obtained from conifer species, is constituted by a group of diterpenes known as abietanes, which, along with its derivatives, has been found to have a wide variety of interesting biological activities, including the antimicrobial, antiviral, antitumoral, and anti-inflammatory activities.

The benzylic oxidation of dehydroabietic acid, an abietane from colophony, and its methyl ester derivative, has been reported using oxidative protocols, such as methyltrioxo-rhenium/ H2O2/pyridine or iodine in aqueous KHCO3.

Herein, we developed an alternative greener protocol for the formation of the benzylic ketone in very good yields using modern electrochemical methods.

Keywords
Benzylic oxidation
Colophony
Dehydroabietic acid
Electrochemistry
Poster
poster_Electrochemical oxidation of abietanes.pdf
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