A gold-catalysed fully intermolecular oxidation and sulfur-ylide formation sequence on ynamides
Research output: Contribution to journal › Article › peer-review
Colleges, School and Institutes
- School of Chemistry; University of Birmingham; Edgbaston Birmingham B15 2TT UK
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.
|Number of pages||4|
|Early online date||16 Apr 2014|
|Publication status||Published - 7 Jun 2014|