The irreversible transesterification of 2-methyl-1,4-butanediol la and its benzyl ethers 2a and 3a catalyzed by Pseudomonas fluorescens lipase in chloroform was studied, the highest ee (>98%) having been obtained for the 4-benzyl ether 2a.

STUDIES ON THE ENANTIOSELECTIVITY OF THE TRANSESTERIFICATION OF 2-METHYL-1,4-BUTANEDIOL AND ITS DERIVATIVES CATALYZED BY PSEUDOMONAS-FLUORESCENS LIPASE IN ORGANIC-SOLVENTS / P. GRISENTI, P. FERRABOSCHI, S. CASATI, E. SANTANIELLO. - In: TETRAHEDRON-ASYMMETRY. - ISSN 0957-4166. - 4:5(1993), pp. 997-1006. [10.1016/S0957-4166(00)80144-5]

STUDIES ON THE ENANTIOSELECTIVITY OF THE TRANSESTERIFICATION OF 2-METHYL-1,4-BUTANEDIOL AND ITS DERIVATIVES CATALYZED BY PSEUDOMONAS-FLUORESCENS LIPASE IN ORGANIC-SOLVENTS

P. FERRABOSCHI
Secondo
;
S. CASATI
Penultimo
;
E. SANTANIELLO
Ultimo
1993

Abstract

The irreversible transesterification of 2-methyl-1,4-butanediol la and its benzyl ethers 2a and 3a catalyzed by Pseudomonas fluorescens lipase in chloroform was studied, the highest ee (>98%) having been obtained for the 4-benzyl ether 2a.
Settore BIO/10 - Biochimica
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/182462
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