4.8 Article

Palladium-catalyzed asymmetric hydrophosphorylation of alkynes: facile access toP-stereogenic phosphinates

期刊

CHEMICAL SCIENCE
卷 11, 期 28, 页码 7451-7455

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d0sc01049a

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资金

  1. National Natural Science Foundation of China [NSFC 21971102]
  2. Guangdong Innovative Program [2019BT02Y335]
  3. AIST

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Despite the importance ofP-chiral organophosphorus compounds in asymmetric catalysis, transition metal-catalyzed methods for accessingP-chiral phosphine derivatives are still limited. Herein, a catalytic enantioselective method for the synthesis ofP-stereogenic alkenylphosphinates is developed through asymmetric hydrophosphorylation of alkynes. This process is demonstrated for a wide range of racemic phosphinates and leads to diverseP-stereogenic alkenylphosphinates directly.

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