Enzymic hydrolysis of methyl 2,3-di-O-acetyl-5-deoxy-α and β-D-xylofuranosides - An active-site model of pig liver esterase

Article abstract of DOI:10.1080/07328309708005734

The regioselective enzymic hydrolysis of methyl 2,3-di-O-acetyl-5-deoxy-α-D-xylofuranoside (1) and methyl 2,3-di-O-acetyl-5-deoxy-β-D-xylofuranoside (2) in the presence of pig liver esterase (PLE) was studied by GLC. Diacetate 2 gave exclusively methyl 3-

Full text of DOI:10.1080/07328309708005734

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Journal of Carbohydrate Chemistry
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Enzymic Hydrolysis of Methyl
2,3-O-Acetyl-5-Deoxy-α and β-D-
Xylofuranosides - An Active-Site Model of
Pig Liver Esterase
a
a
a
Jitka Moravcová , Zita Vanclová , Jindra Čapková , Karel Kefurt
a
a
&
Jan Staněk
a
Department of Chemistry of Natural Compounds , Institute of
Chemical Technology , Technická 5, 166 28, Prague, Czech Republic
Published online: 23 Aug 2006.
To cite this article: Jitka Moravcová , Zita Vanclová , Jindra Čapková , Karel Kefurt & Jan Staněk
(
1997) Enzymic Hydrolysis of Methyl 2,3-O-Acetyl-5-Deoxy-α and β-D-Xylofuranosides - An Active-
Site Model of Pig Liver Esterase, Journal of Carbohydrate Chemistry, 16:7, 1011-1028, DOI:
0.1080/07328309708005734
1
To link to this article: http://dx.doi.org/10.1080/07328309708005734
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