Expanding the chemical diversity of spirooxindoles via alkylative pyridine dearomatization

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Abstract

A mild and practical synthesis of spirooxindole [1,3]oxazino derivatives from N-substituted isatins and 1,3-dicarbonyl compounds with pyridine derivatives is reported. The reactions provided good to excellent yields. Further exploration of the molecular diversity of these compounds is demonstrated through Diels - Alder reactions. © 2012 Dai et al.

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Dai, C., Liang, B., & Stephenson, C. R. J. (2012). Expanding the chemical diversity of spirooxindoles via alkylative pyridine dearomatization. Beilstein Journal of Organic Chemistry, 8, 986–993. https://doi.org/10.3762/bjoc.8.111

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