Several optically active (R)- and (S)-(E)-4-hydroxyalk-2-enoic acids, metabolites of bioactive compounds of lipid peroxidation, were prepared from the corresponding racemic methyl esters by enantioselective hydrolysis mediated by porcine pancreas lipase and porcine liver esterase.

PREPARATION OF (R)-(E)-4-HYDROXY-2-UNSATURATED AND (S)-(E)-4-HYDROXY-2-UNSATURATED ACIDS BY ASYMMETRIC HYDROLYSIS OF THEIR RACEMIC ESTERS / P. ALLEVI, M. ANASTASIA, P. CIUFFREDA, A. SANVITO. - In: TETRAHEDRON-ASYMMETRY. - ISSN 0957-4166. - 4:7(1993), pp. 1397-1400. [10.1016/S0957-4166(00)80324-9]

PREPARATION OF (R)-(E)-4-HYDROXY-2-UNSATURATED AND (S)-(E)-4-HYDROXY-2-UNSATURATED ACIDS BY ASYMMETRIC HYDROLYSIS OF THEIR RACEMIC ESTERS

P. Allevi
Primo
;
M. Anastasia
Secondo
;
P. Ciuffreda
Penultimo
;
1993

Abstract

Several optically active (R)- and (S)-(E)-4-hydroxyalk-2-enoic acids, metabolites of bioactive compounds of lipid peroxidation, were prepared from the corresponding racemic methyl esters by enantioselective hydrolysis mediated by porcine pancreas lipase and porcine liver esterase.
SPAC REACTION ; 4-HYDROXY-(E)-2-ALKENOIC ESTERS ; ALDEHYDES
Settore BIO/10 - Biochimica
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/185076
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