Synthesis of benzosuberone-tethered spirooxindoles: 1-3-dipolar cycloaddition of azomethine ylides and arylidene benzosuberones
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DOI: 10.1007/s11030-018-9901-9
Abstract: Expedient synthesis of benzosuberone-tethered spirooxindoles was accomplished by a three-component 1,3-dipolar cycloaddition reaction between azomethine ylide (generated in situ) and arylidene benzosuberone. This protocol offers good yield and wide functional group tolerance under mild reaction… read more here.
Keywords: benzosuberone tethered; tethered spirooxindoles; benzosuberone; synthesis benzosuberone ... See more keywords