A New Route to E ‐Stilbenes through the Transition‐Metal‐Free KO t Bu/DMF‐Promoted Direct Coupling of Alcohols with Phenyl Acetonitriles
Résumé
An alternative route to synthesise alkenes, based only on the KO t Bu/DMF promoted activation and direct coupling of alcohols with phenyl acetonitriles, is reported. Various E-stilbenes have thus been obtained directly from alcohols that are sustainable sources of carbon, which to our knowledge, is unprecedented in the absence of transition metal based catalysts. A variation allowing, through a Csp 3 À Csp 3 bond formation, the selective synthesis of N-Heteroarenes is also described. A mechanism for the olefination pathway proceeding via an original activation of alcohols under alkyl formates is provided.
Domaines
Chimie organique
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Eur J Org Chem - 2022 - Liu - A New Route to E‐Stilbenes through the Transition‐Metal‐Free KOtBu DMF‐Promoted Direct.pdf (5.48 Mo)
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