Literature DB >> 20515015

Transfer hydrogenation in water: enantioselective, catalytic reduction of alpha-cyano and alpha-nitro substituted acetophenones.

Omid Soltani1, Martin A Ariger, Henar Vázquez-Villa, Erick M Carreira.   

Abstract

Catalytic reduction of alpha-substituted acetophenones under conditions involving asymmetric transfer hydrogenation in water is described. The reaction is conducted in water and open to air, and formic acid is used as reductant.

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Year:  2010        PMID： 20515015     DOI： 10.1021/ol1008894

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


  3 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

2.  Simple and rapid hydrogenation of p-nitrophenol with aqueous formic acid in catalytic flow reactors.

Authors:  Rahat Javaid; Shin-Ichiro Kawasaki; Akira Suzuki; Toshishige M Suzuki
Journal:  Beilstein J Org Chem       Date:  2013-06-14       Impact factor: 2.883

3.  Rigid and concave, 2,4-cis-substituted azetidine derivatives: A platform for asymmetric catalysis.

Authors:  Akina Yoshizawa; Antonio Feula; Louise Male; Andrew G Leach; John S Fossey
Journal:  Sci Rep       Date:  2018-04-25       Impact factor: 4.379
  3 in total

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