One-step direct conversion of a series of heterocyclic aldehydes to heterocyclic esters is reported here by the use of thiamine hydrochloride as a catalyst in the absence of nitrogen atmosphere in a reasonably high yield. This method exclusively produces heterocyclic esters in most cases (specially with more electron-withdrawing heterocyclic aldehydes) without the formation of side products like heteroin. Thus the method developed looks promising and general for the synthesis of electron-withdrawing heterocyclic esters from the corresponding aldehydes.
No takes yet. Share an insight, caveat, or question.
Goswami et al. (2009) studied this question.
Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context: