4.6 Article

Enantioselective hydrogenation of N-heteroaromatics catalyzed by chiral diphosphine modified binaphthyl palladium nanoparticles

Journal

CATALYSIS SCIENCE & TECHNOLOGY
Volume 7, Issue 23, Pages 5515-5520

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7cy01672g

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Funding

  1. National Natural Science Foundation of China (NSFC) [21372118]

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The first application of binaphthyl-stabilized palladium nanoparticles (Bin-PdNPs) with chiral modifiers in asymmetric hydrogenation of N-heteroaromatics is revealed. With an appropriate ratio of R-BINAP/Bin-PdNPs used, the pre-prepared chiral nanocatalyst achieves asymmetric hydrogenations of 2-substituted quinolines with good to excellent yields and moderate enantioselectivities, which showed superior catalytic properties to the R-BINAP/Pd complex. Moreover, this protocol is also applicable to 2-substituted indoles.

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