enzymatic enantioselective hydrolysis of glycidol esters to obtain chiral intermediates for the synthesis of different glycidol-like drugs. Reaction catalysed by efficient immobilized lipases givs high yields and enantiopurity of the product.

"Enantioselective Enzymatic Hydrolysis of Racemic Glycidol Ester by Using Immobilized Porcine Pancreatic Lipase Derivatives with Improved Catalytic Activity"

PREGNOLATO, MASSIMO;TERRENI, MARCO;
2001-01-01

Abstract

enzymatic enantioselective hydrolysis of glycidol esters to obtain chiral intermediates for the synthesis of different glycidol-like drugs. Reaction catalysed by efficient immobilized lipases givs high yields and enantiopurity of the product.
2001
The Chemistry category includes resources that are general in nature and cover a broad spectrum of topics in the chemical sciences. Resources specifically covering analytical chemistry, inorganic and nuclear chemistry, organic chemistry, physical chemistry, and polymer science will be placed in those particular categories. Miscellaneous and applied chemistry resources may be placed in this category when not appropriate for specific subfields in chemistry.
Sì, ma tipo non specificato
Inglese
Internazionale
STAMPA
11
757
763
Tematica Ex SIR: LA Biocatalisi farmaceutica (Classif. Ex SIR:Articoli su riviste ISI ).
Glycidol; esters; hydrolysis; enantioselectivity; lipases
7
info:eu-repo/semantics/article
262
Pregnolato, Massimo; Terreni, Marco; I. E., Fuentes; A. R., ALCANTARA LEON; P., Sabuquillo; R., FERNANDEZ LAFUENTE; J. M., Guisan
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/119444
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