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- W2004162414 abstract "The 1 -aryl-5-phenyltetrazoles (1), in which the 1 -aryl group bears an ortho-methoxycarbonyl, nitro-, carboxamido-, or cyano-group, have been prepared and photolysed. The products are 2-phenylbenzimidazoles (2), which, it is suggested, result from two types of ring-closure of the intermediate benzimidoyl nitrenes : cyclisation at the free ortho-position, or cyclisation at the blocked ortho-position, followed by migration of the substituent from carbon to nitrogen. When the ortho-substituent is a methoxycarbonyl group, the second type of process competes effectively with the first." @default.
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- W2004162414 date "1979-01-01" @default.
- W2004162414 modified "2023-09-27" @default.
- W2004162414 title "Cyclisation of ortho-substituted N-arylbenzimidoyl nitrenes. Part 2. Preferential cyclisations at an ortho-position bearing a methoxycarbonyl group" @default.
- W2004162414 doi "https://doi.org/10.1039/p19790002303" @default.
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