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- W2740417953 abstract "The first solvent-controlled copper-catalyzed oxidative decarboxylative coupling of alkenyl acids with P(O)H compounds for alkenyl C(sp2)−P bond formation by a free-radical process is reported. The reaction enables the highly chemo- and stereoselective synthesis of various (E)-alkenylphosphonates and (E)-alkenylphosphinate oxides in moderate to good yields. On the basis of this catalytic system, styrenes and β-nitrostyrene as well as alkenyl acids can also give the corresponding products by cross-dehydrogenative coupling and denitration, respectively. By altering the oxidant, the oxyphosphorylation of styrenes with P(O)H compounds readily yields β-ketophosphonates. The reaction described here enables a versatile and practical avenue for the formation of valuable C−P bonds." @default.
- W2740417953 created "2017-08-08" @default.
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- W2740417953 date "2017-08-30" @default.
- W2740417953 modified "2023-09-28" @default.
- W2740417953 title "Solvent-Controlled Copper-Catalyzed Radical Decarboxylative Coupling for Alkenyl C(sp<sup>2</sup> )−P Bond Formation" @default.
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- W2740417953 doi "https://doi.org/10.1002/ajoc.201700434" @default.
- W2740417953 hasPublicationYear "2017" @default.
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