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This article is cited in 3 scientific papers (total in 3 papers)
Direct synthesis of 17a-ethoxyimino-8-aza-D-homogonanes by annelation of 3,4-dihydroisoquinolines with 2-acetyl-5,5-dimethyl-3-ethoxyiminocyclohexanone
O. V. Gulyakevich, I. L. Rubinova, D. B. Rubinov, A. L. Mikhal'chuk
Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus, Minsk, Belarus
Abstract:
The annelation reaction of Schiff bases by β,β’-tricarbonyl compounds has been extended to 3-ethoxyimino derivatives of 2-acylcyclohexane-1,3-diones. The first direct synthesis of 8-aza-D-homogonanes with a modified carbonyl group at the pharmacologically significant C(17a) position has been carried out.
Citation:
O. V. Gulyakevich, I. L. Rubinova, D. B. Rubinov, A. L. Mikhal'chuk, “Direct synthesis of 17a-ethoxyimino-8-aza-D-homogonanes by annelation of 3,4-dihydroisoquinolines with 2-acetyl-5,5-dimethyl-3-ethoxyiminocyclohexanone”, Mendeleev Commun., 8:5 (1998), 183–184
Linking options:
https://www.mathnet.ru/eng/mendc4717 https://www.mathnet.ru/eng/mendc/v8/i5/p183
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