Abstract
A method was developed for obtaining the heteroanalogs of steroidal 8-azagonanes using intermediate organoboron compounds with a boron-oxygen bond or esters of boric acid. 8-Azagona-1,3,5(10)-triene, D-homo-8-azagona-1,3,5(10)-triene, and D-dihomo-8-azagona-1,3,5(10)-triene were synthesized.
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
Literature Cited
V. N. Pshenichnyi, N. I. Golub', R. N. Litvinovskaya, and A. A. Akhrem, Vestsi Akad. Nauk BSSR, Ser. Khim. Navuk, No. 4, 96 (1984).
V. V. Gertsev and Ya. Ya. Makarov-Zemlyanskii, Zh. Org. Khim., 5, 178 (1969).
K. Buller and D. Pearson, Organic Syntheses [Russian translation], Vol. 1, Mir, Moscow (1973).
V. S. Markevich, L. I. Gamaga, and I. S. Chichkanova, Zh. Org. Khim., 7, 2078 (1971).
B. P. Tarasevich and E. V. Kuznetsov, Usp. Khim., 56, 353 (1987).
Author information
Authors and Affiliations
Additional information
Translated from Khimiya Geterotsiklicheskhikh Soedinenii, No. 11, pp. 1483–1485, November, 1989.
The authors thank N. N. Chichelova for the 1,5-diketones, which were synthesized in the department of organic chemistry of Vladivostok State University.
Rights and permissions
About this article
Cite this article
Gertsev, V.V., Romanov, Y.A. Organoboron method for the synthesis of 8-azagonanes. Chem Heterocycl Compd 25, 1239–1241 (1989). https://doi.org/10.1007/BF00481517
Received:
Revised:
Issue Date:
DOI: https://doi.org/10.1007/BF00481517