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Regioselective 1,3-dipolar cycloaddition of phenanthrolinium N-ylides to substituted arylidene oxazolones

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Abstract

The 1,3-dipolar cycloaddition reactions of phenanthrolinium ylides have been investigated. Thus 15 novel aryl substituted spiro[oxazole-4,10′-pyrrolo[1,2-a][1,10] phenanthrolin]-5-ones were prepared in a regioselective manner, by the treatment of phenanthrolinium ylides with (Z)-arylidene oxazolones.

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Correspondence to Yaşar Dürüst.

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Dürüst, Y., Sağırlı, A. & Fronczek, F.R. Regioselective 1,3-dipolar cycloaddition of phenanthrolinium N-ylides to substituted arylidene oxazolones. Mol Divers 15, 799–808 (2011). https://doi.org/10.1007/s11030-011-9312-7

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