Abstract
Compounds with a 6-oxa-8-azasteroid skeleton were synthesized from “semicyclic” 1,5-diketones obtained from o-hydroxyacetophenone, formaldehyde, and, respectively, cyclopentanone and 2-methylcyclopentane-1,3-dione.
Similar content being viewed by others
Literature cited
V. I. Alekseev, V. A. Kaminskii, and M. N. Tilichenko, Khim. Geterotsikl. Soedin., 235 (1975).
V. A. Kaminskii and M. N. Tilichenko, Khim. Geterotsikl. Soedin., 1149 (1971).
A. C. Cope and E. C. Herman, J. Amer. Chem. Soc., 72, 3405 (1950).
T. A. Crabb and R. F. Newton, Tetrahedron, 24, 1497, 4423 (1968).
R. C. Cookson and T. A. Crabb, Tetrahedron, 24, 2385 (1968).
M. Uskokovic, H. Bruderer, C. von Planta, T. Williams and A. Brossi, J. Amer. Chem. Soc., 86, 3364 (1964).
N. Bhacca and D. Williams, Applications of NMR Spectroscopy in Organic Chemistry, Holden-Day (1964).
R. E. Brown, D. M. Lustgarten, R. I. Stanaback, and R. I. Meltzer, J. Org. Chem., 31, 1489 (1966).
L. I. Chinn, J. Org. Chem., 27, 54 (1962).
Author information
Authors and Affiliations
Additional information
See [1] for communication XIII.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 239–242, February, 1975.
Rights and permissions
About this article
Cite this article
Donchak, L.N., Kaminskii, V.A. & Tilichenko, M.N. Reactions of 1,5-diketones. Chem Heterocycl Compd 11, 206–208 (1975). https://doi.org/10.1007/BF00471400
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00471400