Tetrabutylammonium iodide-catalyzed radical alkoxycarbonylation of 2-isocyanobiphenyls with carbazates: Synthesis of phenanthridine-6-carboxylates

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Abstract

A practical and environmentally friendly strategy for generating alkoxycarbonyl radicals from readily available carbazates under metal-free conditions has been developed. In the presence of tetrabutylammonium iodide and tert-butyl hydroperoxide, 2-isocyanobiphenyls smoothly underwent radical alkoxycarbonylation with carbazates to afford phenanthridine-6-carboxylates. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Li, X., Fang, M., Hu, P., Hong, G., Tang, Y., & Xu, X. (2014). Tetrabutylammonium iodide-catalyzed radical alkoxycarbonylation of 2-isocyanobiphenyls with carbazates: Synthesis of phenanthridine-6-carboxylates. Advanced Synthesis and Catalysis, 356(9), 2103–2106. https://doi.org/10.1002/adsc.201301158

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