Literature DB >> 15672158

Highly enantioselective hydrogenation of enol ester phosphonates catalyzed by rhodium phosphine-phosphite complexes.

Miguel Rubio1, Andrés Suárez, Eleuterio Alvarez, Antonio Pizzano.   

Abstract

Chiral phosphine-phosphites provide versatile catalysts for the highly enantioselective hydrogenation of alpha-acyloxy alpha, beta-unsaturated phosphonates.

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Year:  2004        PMID： 15672158     DOI： 10.1039/b414288h

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  2 in total

1.  Diametric stereocontrol in dynamic catalytic reduction of racemic acyl phosphonates: divergence from α-keto ester congeners.

Authors:  Michael T Corbett; Jeffrey S Johnson
Journal:  J Am Chem Soc       Date:  2013-01-08       Impact factor: 15.419

2.  Application of phosphine-phosphite ligands in the iridium catalyzed enantioselective hydrogenation of 2-methylquinoline.

Authors:  Miguel Rubio; Antonio Pizzano
Journal:  Molecules       Date:  2010-10-29       Impact factor: 4.411
  2 in total

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