Highly regioselective synthesis of dicyano-8a,10,11-trihydropyrrolo[1,2-a][1,10]phenanthrolines via a domino-Knoevenagel-cyclization |
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Authors: | Reza heydari Batool Tahamipour |
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Affiliation: | Department of Chemistry, The University of Sistan and Baluchestan, P. O. Box 98135-674, Zahedan, Iran |
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Abstract: | 1,10-Phenanthrolinium N-ylides, can react with malonitrile and aromatic aldehydes via a domino-Knoevenagel cyclization to afford a new class of trihydropyrrolo[1,2-a][1,10]phenanthroline derivatives as stable helical compounds in a simple, mild, and efficient protocol in excellent yields. |
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Keywords: | 1,10-Phenanthrolinium N-ylide Domino-Knoevenagel-cyclization Trihydropyrrolo[1,2-a][1,10]phenanthrolines Multicomponent reaction |
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