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Published on: December 29, 2016
Synthesis and Reactivity of 3,3-Diazidooxindoles
Kristina Holzschneider1, Fabian Mohr, Stefan F Kirsch1
1Organic Chemistry , Bergische Universität Wuppertal , Gaußstr. 20 , 42119 Wuppertal , Germany.
Abstract:
The synthesis of previously unknown 3,3-diazidooxindoles as synthetically useful derivatives of isatins was accomplished through the direct oxidative diazidation of 2-oxindoles. The method yielded the diazido compounds from the starting oxindoles under mild and simple conditions with NaN3 and iodine, in good yields. The notable reactivity of this new class of compounds toward primary and secondary nucleophilic amines is also described, which gives access to either 4-imino-3,4-dihydroquinazolin-2(1 H)-one derivatives or cyanophenylureas.
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