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)-2,3-EPOXY-2-(4-PENTENYL)-PROPANOL, AND (S)-2,3-EPOXY-2-(4-PENTENYL)-PROPANOL, A CHIRAL BUILDING BLOCK FOR THE SYNTHESIS OF (R)-FRONTALIN 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)-2,3-EPOXY-2-(4-PENTENYL)-PROPANOL, AND (S)-2,3-EPOXY-2-(4-PENTENYL)-PROPANOL, A CHIRAL BUILDING BLOCK FOR THE SYNTHESIS OF (R)-FRONTALIN AND (S)-FRONTALIN
P. FERRABOSCHIPrimo
;S. CASATISecondo
;E. SANTANIELLOUltimo
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.
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