Literature DB >> 15496110

Asymmetric hydrogenation of ketones using a ruthenium(II) catalyst containing BINOL-derived monodonor phosphorus-donor ligands.

Yingjian Xu1, Nat W Alcock, Guy J Clarkson, Gordon Docherty, Gary Woodward, Martin Wills.   

Abstract

[structure: see text] A series of ruthenium(II) complexes containing BINOL-based monodonor phosphorus ligands have been prepared and applied to the asymmetric catalysis of the hydrogenation of aryl/alkyl ketones. The best ligands for this application are those which contain an aromatic groups with either a methoxide or bromide on the ortho position. Using these ligands, alcohols with ee's of up to 99% are formed.

Entities:  

Year:  2004        PMID: 15496110     DOI: 10.1021/ol0481840

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  1 in total

1.  New phosphine-diamine and phosphine-amino-alcohol tridentate ligands for ruthenium catalysed enantioselective hydrogenation of ketones and a concise lactone synthesis enabled by asymmetric reduction of cyano-ketones.

Authors:  José A Fuentes; Scott D Phillips; Matthew L Clarke
Journal:  Chem Cent J       Date:  2012-12-10       Impact factor: 4.215

  1 in total

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