Enantioselective synthesis of α-hydroxy phosphonates via oxidation with (camphorsulfonyl)oxaziridines

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Abstract

Reaction of phosphonate anions with enantiomerically pure (camphorsulfonyl)oxaziridines results in formation of nonracemic α-hydroxy phosphonates. This enantioselective hydroxylation methodology provides convenient access to optically active α-hydroxy phosphonates and their corresponding phosphonic acids.

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Pogatchnik, D. M., & Wiemer, D. F. (1997). Enantioselective synthesis of α-hydroxy phosphonates via oxidation with (camphorsulfonyl)oxaziridines. Tetrahedron Letters, 38(20), 3495–3498. https://doi.org/10.1016/S0040-4039(97)00705-3

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