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Journal of the American Chemical Society, Vol.133, No.40, 15797-15799, 2011
Total Synthesis of (-)-N-Methylwelwitindolinone C Isothiocyanate
We report the first total synthesis of (-)-N-methylwelwitindolinone C isothiocyanate. Our route features a number of key transformations, including an indolyne cyclization to assemble the [4.3.1]-bicyclic scaffold, as well as a late-stage intramolecular nitrene insertion to functionalize the C11 bridgehead carbon en route to the natural product.