Highly regioselective synthesis of dicyano-8a, 10,11-trihydropyrrolo [1,2-a][1,10]phenanthrolines vi

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1,10-Phenanthrolinium N-ylides, can react with malonitrile and aromatic aldehydes via a domino-Knoevenagel cyclization to afford a new class of mhydropyrrolo[l,2-a][l,10]phenanthroline derivatives as stable helical compounds in a simple, mild, and efficient protocol in excellent yields.
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