Abstract
A new method for synthesizing 17β-amino-5α-androstane was developed based on tigogenin. The configuration at C-17 was proved by PMR.
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REFERENCES
T. J. Campbell and E. M. V. Williams, Brit. J. Pharmacol., 76, 337 (1982).
R. A. Lucas, D. F. Dickel, R. L. Dziemian, M. J. Ceglowski, B. L. Hensle, and H. B. McPhillamy, J. Am. Chem. Soc., 82, No. 21, 5688 (1960).
J. C. Babcock, U.S. Pat. No. 3,009,925 (1961); Chem. Abstr., 56, P10234f (1962).
R. E. Marker, J. Am. Chem. Soc., 58, 480 (1936).
C. W. Choppe and J. C. P. Sly, J. Chem. Soc., 345 (1959).
J. C. Babcock, U.S. Pat. No. 2,863,885 (1958); Chem. Abstr., 54, P2440f (1960).
E. P. Kemertelidze and T. A. Pkheidze, Khim.-Farm. Zh., 6, No. 12, 44 (1972).
W. H. Kruizinga, B. Strijtveen, and R. M. Kellogg, J. Org. Chem., 46, 4321 (1981).
S. Takasuto and N. Ikekawa, Chem. Pharm. Bull., 23, No. 12, 1431 (1989).
N. Sh. Nadaraia, V. I. Sladkov, L. N. Kuleshova, and N. N. Suvorov, Zh. Org. Khim., 23, No. 3, 533 (1987).
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Merlani, M.I., Davitishvili, M.G., Nadaraia, N.S. et al. Conversion of Epiandrosterone Into 17β-Amino-5α-androstane. Chemistry of Natural Compounds 40, 144–146 (2004). https://doi.org/10.1023/B:CONC.0000033931.36367.0d
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DOI: https://doi.org/10.1023/B:CONC.0000033931.36367.0d