Microbial transformation of 19-hydroxypregnanes.
نویسندگان
چکیده
Nocardia species aromatized 19-hydroxyprogesterone, 3beta, 19-dihydroxy-pregn-5-en-20-one 3-acetate and pregn-5-ene-3beta, 19, 20beta-triol 3-acetate, without cleavage of the side chain, into 3-hydroxy-19-norpregna-1,3,5 (10)-trien-20-one. Septomyxa affinis aromatized the ring A and cleaved the side chain of 19-hydroxyprogesterone to yield estrone. With 19-hydroxypregna-4, 7-diene-3, 20-dione as substrate, the transformation was more complex and many products were formed.
منابع مشابه
Mercuric Oxide-Iodine Oxidation of 6/^-Hydroxypregnanes. Influence of the C-5 Functionality
Adriana L. Brachet-Cota and Gerardo Burton* Departamento de Qirimica Orgänica, Facultad de Cieneias Exaetas y Naturales, Universidad de Buenos Aires, Pabellön 2, Ciudad Universitaria, 1428 Buenos Aires, Argentina Z. Naturforsch. 43b, 491-495 (1988); received November 2, 1987 6/3-Hydroxypregnanes, Mercuric Oxide, Oxidation, /3-Fragmentation. Hypoiodite Reaction Oxidation of 6/3-hydroxyprogestero...
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ورودعنوان ژورنال:
- Applied microbiology
دوره 20 1 شماره
صفحات -
تاریخ انتشار 1970