Reaction of 3-aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones with substituted acetamides of 3,4-dihydroisoquinolines

Autor:	A. V. Kharitonova, V. V. Konovalova, A. N. Maslivets, Yu. V. Shklyaev
Rok vydání:	2015
Předmět:	chemistry.chemical_compound Chemistry Organic Chemistry Medicinal chemistry Acetamide Pyrrole
Zdroj:	Russian Journal of Organic Chemistry. 51:1566-1571
ISSN:	1608-3393 1070-4280
DOI:	10.1134/s1070428015110081
Popis:	3-Aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones react with substituted [3,4-dihydroisoquinolin-1(2H)-ylidene]acetamides and {2,3-dihydrobenzo[f]isoquinolin-4(1H)-ylidene}acetamide to produce substituted 1,5,5',6'-tetrahydro-3'H-spiro(pyrrole-2,2'-pyrrolo[2,1-a]-isoquinoline)-1'-carboxamides and 13-aza-analogs of steroids, substituted 5H-spiro(benzo[f]pyrrolo[2,1-a]isoquinoline-9,2'-pyrrole)-10-carboxamides respectively.
Databáze:	OpenAIRE
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