The irreversible transesterification of racemic 2-methyl-1,3-propanediol derivatives, the monoethers 3a, 3b, 5a, and the monobenzoate 5b, with vinyl acetate catalyzed by Pseudomonas fluorescens lipase in chloroform affords enantiomerically pure chiral synthons.

ENANTIOSELECTIVE TRANSESTERIFICATION OF 2-METHYL-1,3-PROPANEDIOL DERIVATIVES CATALYZED BY PSEUDOMONAS-FLUORESCENS LIPASE IN AN ORGANIC-SOLVENT / P. GRISENTI, P. FERRABOSCHI, A. MANZOCCHI, E. SANTANIELLO. - In: TETRAHEDRON. - ISSN 0040-4020. - 48:18(1992), pp. 3827-3834.

ENANTIOSELECTIVE TRANSESTERIFICATION OF 2-METHYL-1,3-PROPANEDIOL DERIVATIVES CATALYZED BY PSEUDOMONAS-FLUORESCENS LIPASE IN AN ORGANIC-SOLVENT

P. FERRABOSCHI
Secondo
;
A. MANZOCCHI
Penultimo
;
E. SANTANIELLO
Ultimo
1992

Abstract

The irreversible transesterification of racemic 2-methyl-1,3-propanediol derivatives, the monoethers 3a, 3b, 5a, and the monobenzoate 5b, with vinyl acetate catalyzed by Pseudomonas fluorescens lipase in chloroform affords enantiomerically pure chiral synthons.
Settore BIO/10 - Biochimica
Article (author)
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

Caricamento pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/181120
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 37
  • ???jsp.display-item.citation.isi??? 34
social impact