A mild and quantitative procedure for the removal of nucleoside alkoxycarbonyl groups using pig liver esterase or Candida antarctica B lipase

2005 ◽  
Vol 36 (1-6) ◽  
pp. 36-39 ◽  
Author(s):  
Mariana Capello ◽  
Mariana González ◽  
Silvio D. Rodríguez ◽  
Luis E. Iglesias ◽  
Adolfo M. Iribarren
2009 ◽  
Vol 61 (3-4) ◽  
pp. 241-246 ◽  
Author(s):  
Kalliopi Thodi ◽  
Efrosini Barbayianni ◽  
Irene Fotakopoulou ◽  
Uwe T. Bornscheuer ◽  
Violetta Constantinou-Kokotou ◽  
...  

2016 ◽  
Vol 124 ◽  
pp. 52-61 ◽  
Author(s):  
Nadia Ligianara D. Nyari ◽  
Ilizandra A. Fernandes ◽  
Cindy E. Bustamante-Vargas ◽  
Clarisse Steffens ◽  
Débora de Oliveira ◽  
...  

Author(s):  
D. Jonathan Bennett ◽  
Kirsteen I. Buchanan ◽  
Andrew Cooke ◽  
Ola Epemolu ◽  
Niall M. Hamilton ◽  
...  

1985 ◽  
Vol 63 (2) ◽  
pp. 452-456 ◽  
Author(s):  
J. Bryan Jones ◽  
R. Scott Hinks ◽  
Philip G. Hultin

Preparative-scale pig liver esterase-catalyzed hydrolyses of five-membered ring meso-1,3-diesters are enantiotopically selective. While pro-S enantiotopic selectivity is exhibited in each case, the absolute configuration sense of the hydrolysis in the cyclopentyl series is opposite to that of both the tetrahydrofuranyl and tetrahydrothiophenyl diesters. The enantiomeric excess levels induced are in the 34–46% range.


1989 ◽  
Vol 54 (21) ◽  
pp. 5115-5122 ◽  
Author(s):  
Hans Joachim Gais ◽  
Gerd Buelow ◽  
Andrzej Zatorski ◽  
Mathias Jentsch ◽  
Peter Maidonis ◽  
...  

Tetrahedron ◽  
2008 ◽  
Vol 64 (37) ◽  
pp. 8947-8951 ◽  
Author(s):  
Long Yi ◽  
Li Cao ◽  
Liangliang Liu ◽  
Zhen Xi

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