Benylic, allylic, and propargylic alcohols, as well as diols, can be oxidized with o-iodoxybenzoic acid (IBX) in the presence of stabilized Wittig ylide[1] Maryanoff, B. E. and Reitz, A. B. 1989. Chem. Rev., : 863[Crossref], [Web of Science ®] , [Google Scholar] to generate α,β-unsaturated ester in one pot. This is useful when the intermediate aldehydes are unstable and difficult to isolate.
No takes yet. Share an insight, caveat, or question.
Maiti et al. (2001) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: