We report an aqueous phosphoric acid-promoted [3,3]-sigmatropic rearrangement of 2-(furan-3-yl)-2-(arylamino)acetonitriles for the regioselective synthesis of polysubstituted 2-arylfurans. This transition-metal-free method proceeds under mild, room-temperature conditions with broad functional-group tolerance. The utility of these products is showcased through their efficient one-step transformation into previously undescribed 5,6-dihydro-4H-benzo[ b ]furo[2,3- d ]azepine derivatives. This approach aligns with green chemistry principles and expands the synthetic utility of heteroaromatic rearrangements.
No takes yet. Share an insight, caveat, or question.
Buravov et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: