Reply to the ‘Comment on “Dithiocarbamate-mediated thioamidation of arylglyoxylic acids by decarboxylative–decarbonylative C–C bond formation reactions”’ by X. Creary, Org. Chem. Front. , 2026, 13 , DOI: 10.1039/D4QO00393D | Synapse
March 19, 2026Organic Chemistry Frontiers1 citations
Reply to the ‘Comment on “Dithiocarbamate-mediated thioamidation of arylglyoxylic acids by decarboxylative–decarbonylative C–C bond formation reactions”’ by X. Creary, Org. Chem. Front. , 2026, 13 , DOI: 10.1039/D4QO00393D
To confirm the reproducibility of the thioamidation protocol for arylglyoxylic acids.
Reproduced thioamidation protocol by our research group.
Collaborated with another research group from a different institute.
Thioamidation process was successfully replicated.
Consistency in results confirmed by multiple research groups.
Abstract
The thioamidation protocol of arylglyoxylic acids has been reproduced satisfactorily by our research group as well as by another research group from a different institute.