Abstract
4-Ethoxycarbonyl-5-phenyl-substituted 1H-pyrrole-2,3-diones react with 3-arylamino-1H-inden-1-ones in the ratios 1: 1 and 1: 2 to form substituted spiro{indeno[1,2-b]quinoline-10,3′-pyrroles} and substituted spiro{diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles}, respectively.
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Dedicated to Academician of the Russian Academy of Sciences V. N. Charushin on the occasion of his 60th birthday.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 58—62, January, 2012.
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Dmitriev, M.V., Silaichev, P.S., Aliev, Z.G. et al. Two directions in spiroheterocyclization of 1H-pyrrole-2,3-diones upon the action of 3-arylamino-1H-inden-1-ones. Russ Chem Bull 61, 59–63 (2012). https://doi.org/10.1007/s11172-012-0009-6
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DOI: https://doi.org/10.1007/s11172-012-0009-6