N-heterocyclic carbene-catalyzed domino hydroacylation/stetter reactions of salicyl alkynylphosphonates and aromatic aldehydes

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Abstract

1,4-Dicarbonyl compounds 2 carrying a phosphonate group were obtained by utilizing a dually N-heterocyclic carbene (NHC) catalyzed domino reaction involving the intramolecular hydroacylation of salicyl alkynylphosphonates 1 and a subsequent intermolecular Stetter reaction with aromatic aldehyde at room temperature. In addition, 2 can also be applied for the synthesis of benzopyranopyrrole carrying a phosphonate group 4 in one pot and in moderate yield. ©ARKAT-USA, Inc.

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Wang, Z. Q., Wang, Y., & Shi, D. Q. (2013). N-heterocyclic carbene-catalyzed domino hydroacylation/stetter reactions of salicyl alkynylphosphonates and aromatic aldehydes. Arkivoc, 2013(4), 88–97. https://doi.org/10.3998/ark.5550190.p008.158

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