The biohydrogenation of 2-substituted allyl alcohols 1a-c proceeds enantioselectively (95-98% ee) to afford (R)-2-methyl alkanols 2a-c.
BAKERS YEAST-MEDIATED HYDROGENATION OF 2-SUBSTITUTED ALLYL ALCOHOLS - A BIOCATALYTIC ROUTE TO A NEW HIGHLY ENANTIOSELECTIVE SYNTHESIS OF (R)-2-METHYL ALKANOLS / P. FERRABOSCHI, S. CASATI, E. SANTANIELLO. - In: TETRAHEDRON-ASYMMETRY. - ISSN 0957-4166. - 5:1(1994), pp. 19-20. [10.1016/S0957-4166(00)80474-7]
BAKERS YEAST-MEDIATED HYDROGENATION OF 2-SUBSTITUTED ALLYL ALCOHOLS - A BIOCATALYTIC ROUTE TO A NEW HIGHLY ENANTIOSELECTIVE SYNTHESIS OF (R)-2-METHYL ALKANOLS
P. FERRABOSCHIPrimo
;S. CASATISecondo
;E. SANTANIELLOUltimo
1994
Abstract
The biohydrogenation of 2-substituted allyl alcohols 1a-c proceeds enantioselectively (95-98% ee) to afford (R)-2-methyl alkanols 2a-c.
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