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Mendeleev Communications, 1999, Volume 9, Issue 5, Pages 208–209
DOI: https://doi.org/10.1070/MC1999v009n05ABEH001091 (Mi mendc4600) 		 
This article is cited in 7 scientific papers (total in 7 papers)

Heteroannelation of 3,4-dihydroisoquinoline with (3H,5H)-3-acylthiophene-2,4-diones: one-stage synthesis of new heterocyclic steroid analogues, 8-aza-16-thiagonanes

M. V. Budnikova, D. B. Rubinov, L. G. Lis, A. L. Mikhal'chuk

Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus, Minsk, Belarus
Full-text PDF (147 kB) Citations (7)
DOI: https://doi.org/10.1070/MC1999v009n05ABEH001091
Abstract: New 8-aza-16-thiasteroid analogues, benzo[a]thieno[f]quinolizines, have been synthesised by the [2 + 4] heteroannelation of 3,4-dihydroisoquinoline with 3-acylthiotetronic acids.
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Document Type: Article
Language: English


Citation: M. V. Budnikova, D. B. Rubinov, L. G. Lis, A. L. Mikhal'chuk, “Heteroannelation of 3,4-dihydroisoquinoline with (3H,5H)-3-acylthiophene-2,4-diones: one-stage synthesis of new heterocyclic steroid analogues, 8-aza-16-thiagonanes”, Mendeleev Commun., 9:5 (1999), 208–209
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    • This publication is cited in the following 7 articles:
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