ChemInform Abstract: Pig Liver Esterase Catalyzed Hydrolyses of Diesters. A New Route to the Syntheses of Achiral Half-Esters.

ChemInform ◽  
2010 ◽  
Vol 26 (27) ◽  
pp. no-no
Author(s):  
D. J. AGER ◽  
I. PRAKASH
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

ChemInform ◽  
2010 ◽  
Vol 22 (37) ◽  
pp. no-no
Author(s):  
F. J. C. VAN GASTEL ◽  
A. J. H. KLUNDER ◽  
B. ZWANENBURG

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