Enantiomerically pure (R)- and (S)-epoxyalcohols 1, chiral intermediates for the synthesis of (R)- and (S)-frontalin 2, are prepared by Pseudomonas fluorescens lipase-catalyzed transesterification in dichloromethane.
A chemoenzymatic approach to enantiomerically pure (R)- and (S)-2,3-epoxy-2-(4-pentenyl)-propanol, a chiral building block for the synthesis of (R)- and (S)-frontalin / P. Ferraboschi, S. Casati, P. Grisenti, E. Santaniello. - In: TETRAHEDRON-ASYMMETRY. - ISSN 0957-4166. - 4:1(1993), pp. 9-12. [10.1016/S0957-4166(00)86004-8]
A chemoenzymatic approach to enantiomerically pure (R)- and (S)-2,3-epoxy-2-(4-pentenyl)-propanol, a chiral building block for the synthesis of (R)- and (S)-frontalin
P. FerraboschiPrimo
;S. CasatiSecondo
;E. Santaniello
Ultimo
1993
Abstract
Enantiomerically pure (R)- and (S)-epoxyalcohols 1, chiral intermediates for the synthesis of (R)- and (S)-frontalin 2, are prepared by Pseudomonas fluorescens lipase-catalyzed transesterification in dichloromethane.
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.
