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Ring Opening of Organosilicon-Substituted Benzoxazolinone: A Convenient Route to Chelating Ureato and Carbamido Ligands

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posted on 22.12.2008, 00:00 by Jörg Wagler, Anthony F. Hill
N-Silylated benzoxazolin-2-one reacts with N−H and C−H acidic heterocycles (benzoxazolinone, 3,5-dimethylpyrazole, N-methylimidazole) under benzoxazolinone ring cleavage and formation of ortho-siloxyphenyl-substituted ureas and carbamides, respectively. These products were shown to serve as sources for tridentate (O′NO) and (N′NO) chelating ligands.

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