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. FERRABOSCHI
Primo
;
S. CASATI
Secondo
;
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.
Settore BIO/10 - Biochimica
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/2434/182457
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