Two directions in spiroheterocyclization of 1H-pyrrole-2,3-diones upon the action of 3-arylamino-1H-inden-1-ones View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2012-01

AUTHORS

M. V. Dmitriev, P. S. Silaichev, Z. G. Aliev, S. M. Aldoshin, A. N. Maslivets

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.

PAGES

59-63

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-012-0009-6

DOI

http://dx.doi.org/10.1007/s11172-012-0009-6

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1052950087


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