The Pseudomonas cepacia Iipase preferentially acylates the 2'-regioisomers of a few 1'-and 2'-naphthyl alcohols; the case of compounds 3a, 3c, 4a, 4e the (R)-alcohols (65->98% ee) and the (S)-acetates (62-98% ee) are formed.
Studies on the regio- and enantioselectivity of the lipase-catalyzed transesterification of 1′- and 2′-naphthyl alcohols in organic solvent / P. Ferraboschi, S. Casati, A. Manzocchi, E. Santaniello. - In: TETRAHEDRON-ASYMMETRY. - ISSN 0957-4166. - 6:7(1995), pp. 1521-1524. [10.1016/0957-4166(95)00188-U]
Studies on the regio- and enantioselectivity of the lipase-catalyzed transesterification of 1′- and 2′-naphthyl alcohols in organic solvent
P. FerraboschiPrimo
;S. CasatiSecondo
;A. ManzocchiPenultimo
;E. SantanielloUltimo
1995
Abstract
The Pseudomonas cepacia Iipase preferentially acylates the 2'-regioisomers of a few 1'-and 2'-naphthyl alcohols; the case of compounds 3a, 3c, 4a, 4e the (R)-alcohols (65->98% ee) and the (S)-acetates (62-98% ee) are formed.
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