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. FERRABOSCHISecondo
;S. CASATIPenultimo
;E. SANTANIELLOUltimo
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.
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
