A gold-catalysed fully intermolecular oxidation and sulfur-ylide formation sequence on ynamides

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Abstract

An efficient C–O, C–S and C–C bond-forming sequence leads to functionalised compounds bearing sulfur-substituted quaternary carbons. Ynamides are employed as diazo-equivalents to access the [2,3]-sigmatropic rearrangements of allyl sulfonium ylides by a three-component chemoselective oxidation and intermolecular ylide formation. © 2014 The Partner Organisations.

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Santos, M. D., & Davies, P. W. (2014). A gold-catalysed fully intermolecular oxidation and sulfur-ylide formation sequence on ynamides. Chemical Communications, 50(45), 6001–6004. https://doi.org/10.1039/c4cc01059k

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