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The photochemical and mass spectral properties of 5-phenoxy-1-phenyl-1H-tetrazole
Journal of the Chemical Society D: Chemical Communications Pub Date : , DOI:10.1039/C2969001110B
Abstract

The formation of a benzimidazole (III) or pseudourea derivative (IV) when the starting tetrazole (I) is irradiated in different solvents is attributed to an azomethine biradical or nitrene intermediate and the mass spectral properties of (I) and (III) indicate a novel 1,3-ON phenyl migration.

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