Microbiological transformations of 19-oxygenated ent-kauranes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. The microbiological hydroxylation of steroids and related compounds
2. Microbiological hydroxylation of steroids. Part XI. Convenient routes to 3,7-, 3,11-, 3,12-, 7,11-, 7,17-, and 11,17-dioxygenated 5α-androstanes and to 5α-androstan-11-one
3. Microbiological transformations of tetracyclic diterpenes
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1. Synthetic Transformations of Ent-Kaurenoic Acid;Chemistry Journal of Moldova;2015-06
2. The Remarkable Structural Diversity Achieved in ent-Kaurane Diterpenes by Fungal Biotransformations;Molecules;2014-02-10
3. Discovery and structure–activity relationships of ent-Kaurene diterpenoids as potent and selective 11β-HSD1 inhibitors: Potential impact in diabetes;European Journal of Medicinal Chemistry;2013-07
4. Diterpenes from Sideritis infernalis and S. candicans;Zeitschrift für Naturforschung B;2008-05-01
5. A simple synthesis of kaurenoic esters and other derivatives and evaluation of their antifungal activity;Journal of the Brazilian Chemical Society;2005-11
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