Microbial hydroxylation of 13-ethyl-17β-hydroxy-18,19-dinor-17α-pregn-4-en-20-yn-3-one
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry
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2. A partial synthesis of 13-ethyl-1 1-methylene-18,19-dinor-17α-pregn-4-en-20-yn-17-ol (desogestrel) based upon intramolecular oxidation of an 11β-hydroxy-19-norsteroid to the 18 → 11β-lactone;Van den Heuvel;Recl Trav Chim Pays-Bas,1988
3. Synthesis of 13-Ethyl-11-methylene-18,19-dinor-17α-pregn-4-en-20-yn-17-ol (desogestrel) and its main metabolite 3-oxo desogestrel;Schwarz;Tetrahedron,1994
4. Microbiological conversion of 19-nortestosterone (II) 10- and 11-hydroxylation;De Flines;Recueil,1963
5. Substituent effects in the 13C NMR spectra of 17α-ethinyl-19-nortestosterone derivatives;Hammann;Magn Reson Chem,1990
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