Effect of the amount of lipase on enantioselectivity in the kinetic resolution by enzymatic acylation of arylalkylcarbinols

Merabet-Khelassi, Mounia;Bouzemi, Nassima;Fiaud, Jean-Claude;Riant, Olivier;Aribi-Zouioueche, Louisa
(2011) Comptes rendus. Chimie — Vol. 14, n° 11, p. 978-986 (2011)

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Authors
  • Merabet-Khelassi, Mounia
    Author
  • Bouzemi, Nassima
    Author
  • Fiaud, Jean-Claude
    Author
  • Author
  • Aribi-Zouioueche, Louisa
    Author
Abstract
This study shows the influence of the amount of Candida Antarctica-B lipase on reactivity and selectivity in lipase-catalyzed acylation of arylalkylcarbinols 1-8. For 1-indanol 1 and with isopropenyl acetate, the selectivity E increases from 60 to > 500 when the amount of the lipase decreases from 150 to 3 mg. For the 1,2,3,4-tetrahydronaphthalen-1-ol 4, in the presence of succinic anhydride, the decrease of the amount of Candida Antarctica-B from 150 to 20 mg brings an improvement of the selectivity from E = 50 to E = 140. For the acylation of α-hydroxyferrocene 8 with vinyl acetate, high selectivities are reached with the lipases of Candida Antarctica-B, C = 50% E > 500 and Pseudomonas cepacia, C = 42% E = 425. The reduction of the amount of CAL-B, in toluene, results in an increase of the selectivity of acylation of ferrocenylethanol 8, from E = 20 to E > 500. This effect is not displayed in di-isopropylether. © 2011 Académie des sciences. Published by Elsevier Masson SAS. All rights reserved.
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  • Institution iconUCLouvainSST/IMCN/MOST - Molecules, Solids and Reactivity

Citations

Merabet-Khelassi, M., Bouzemi, N., Fiaud, J.-C., Riant, O., & Aribi-Zouioueche, L. (2011). Effect of the amount of lipase on enantioselectivity in the kinetic resolution by enzymatic acylation of arylalkylcarbinols. Comptes rendus. Chimie, 14(11), 978-986. https://doi.org/10.1016/j.crci.2011.07.005 (Original work published 2011)