Literature DB >> 11349901

Asymmetric nickel-catalyzed hydrocyanation of vinylarenes by applying homochiral xantphos ligands.

W Goertz1, P C Kamer, P W van Leeuwen, D Vogt.   

Abstract

New homochiral xantphos-type diphosphonite ligands with binaphthoxy substituents have been prepared and characterized by NMR spectroscopy. These ligands have been applied in the nickel-catalyzed hydrocyanation of styrene and other vinylarenes. Enantioselectivities up to 63% ee have been obtained by using 4-isobutylstyrene as a substrate. Addition of an excess of ligand strongly inhibits the hydrocyanation reaction since the bis-chelate nickel complexes formed are highly stable and catalytically inactive.

Entities:  

Year:  2001        PMID: 11349901     DOI: 10.1002/1521-3765(20010417)7:8<1614::aid-chem16140>3.0.co;2-e

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  Intramolecular hydroamination of unbiased and functionalized primary aminoalkenes catalyzed by a rhodium aminophosphine complex.

Authors:  Lisa D Julian; John F Hartwig
Journal:  J Am Chem Soc       Date:  2010-10-06       Impact factor: 15.419

2.  Synthesis, mechanism of formation, and catalytic activity of Xantphos nickel π-complexes.

Authors:  Nicholas D Staudaher; Ryan M Stolley; Janis Louie
Journal:  Chem Commun (Camb)       Date:  2014-10-30       Impact factor: 6.222

  2 in total

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