Summary
1. The 11α-hydroxylation of 16α, 17α-dimethylprogesterone has been effected by the strain ofRhizopus nigricans VNIKhFI-7 with a yield of hydroxy derivative of 61%.
2. In the transformation an unidentified dihydroxy compound is formed together with the 11α-hydroxy-16α, 17α-dimethylprogesterone.
Similar content being viewed by others
Literature cited
V. I. Maksimov, F. A. Lur'i, and L. S. Morozova, Zh. Obshch. Khim.,33, 1666 (1963).
N. N. Suvorov, Med. Prom. SSSR, No. 3, 22 (1956).
A. G. Timofeeva, O. S. Madaeva, E. G. Gusakova, N. F. Kovylkina, N. I. Men'shova, and V. M. Novikova, Izv. Akad. Nauk SSSR, Ser. Biol., No. 6, 712 (1958).
W. P. Schneider, F. H. Lincoln, G. B. Spero, H. C. Muffay, and I. L. Thomson, J. Amer. Chem. Soc.,81, 3167 (1959).
V. M. Ryzhkova, K. N. Gabinskaya, V. F. Shner, and N. N. Suvorov, Mikrobiol. Prom. SSSR, No. 2, 23 (1970).
N. Bhacca and D. Williams, Applications of NMR Spectroscopy in Organic Chemistry, Holden-Day, San Francisco (1964).
Additional information
S. Ordzhonikidze All-Union Scientific-Research Institute of Pharmaceutical Chemicals. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 46–48, January–February, 1973.
Rights and permissions
About this article
Cite this article
Morozova, L.S., Gabinskaya, K.N. & Grinenko, G.S. Microbiological hydroxylation of 16α, 17α-dimethylprogesterone. Chem Nat Compd 9, 39–40 (1973). https://doi.org/10.1007/BF00580886
Received:
Published:
Issue Date:
DOI: https://doi.org/10.1007/BF00580886