Synthesis of unsymmetrical ketones via simple C-H activation of aldehydes and concomitant hydroacylation of vinyl sulfonates.
ORG BIOMOL CHEM
235 - 237.
A new and simple protocol for the direct functionalisation of aldehydes with concomitant conversion into ketones via C-C bond formation has been developed. The reaction effectively enables the direct C-H activation of an aldehyde by mixing of an aldehyde and a vinyl sulfonate under aerobic conditions or using hydrogen peroxide as a sub-stoichiometric reagent.
|Title:||Synthesis of unsymmetrical ketones via simple C-H activation of aldehydes and concomitant hydroacylation of vinyl sulfonates|
|Keywords:||POLARITY-REVERSAL CATALYST, N-HYDROXYPHTHALIMIDE NHPI, RADICAL-CHAIN ADDITION, INTERMOLECULAR HYDROACYLATION, ACYL RADICALS, ALKENES, SULFONAMIDES, ESTERS, DERIVATIVES, AMINOLYSIS|
|UCL classification:||UCL > School of BEAMS > Faculty of Maths and Physical Sciences > Chemistry
UCL > VP Enterprise
Archive Staff Only