Exploratory photochemistry of iodinated aromatic azides

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Abstract

In contrast to the photolysis of p-toluyl azide, photolysis of ortho- or meta-iodo substituted p-toluyl azide in the presence of nucleophilic trapping agents produced the corresponding triplet nitrene which led to the simple aniline products and not to the dehydroazepine-nucleophile adducts. © 1989.

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Watt, D. S., Kawada, K., Leyva, E., & Platz, M. S. (1989). Exploratory photochemistry of iodinated aromatic azides. Tetrahedron Letters, 30(8), 899–902. https://doi.org/10.1016/S0040-4039(00)95273-0

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