Lipase-catalyzed kinetic resolution of 3-hydroxy esters in organic solvents and supercritical carbon dioxide

Research output: Contribution to journalArticleResearchpeer review

Authors

  • A. Capewell
  • V. Wendel
  • Uwe T. Bornscheuer
  • H. H. Meyer
  • T. Scheper

Research Organisations

External Research Organisations

  • University of Stuttgart
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Details

Original languageEnglish
Pages (from-to)181-186
Number of pages6
JournalEnzyme and microbial technology
Volume19
Issue number3
Publication statusPublished - 15 Aug 1996

Abstract

The lipase-catalyzed kinetic resolution of different 3-hydroxy esters in organic solvents and supercritical carbon dioxide (SCCO2) was studied. Similar enantiomeric excesses (ee, up to 99%) as found for transesterifications in organic solvents were achieved also in SCCO2. The influence of various reaction parameters was investigated for the resolution of 3-hydroxy octanoic acid methyl esters with lipase from Pseudomonas cepacia in SCCO2. Optimum conditions have been found at 11O bar, 40°C, and in the presence of 1.5 g molecular sieve by using vinyl acetate as acyl donor. The addition of different cosolvents had only a small effect on the reaction. Immobilization of the lipase on VA-epoxy resulted in similar optical purities as found for the elude lipase, but at halved reaction times. The effect of supercritical conditions on the stability of the lipase was also investigated.

Keywords

    3-hydroxy esters, Kinetic resolution, Lipase, Organic solvents, Pseudomonas cepacia, Supercritical carbon dioxide

ASJC Scopus subject areas

Cite this

Lipase-catalyzed kinetic resolution of 3-hydroxy esters in organic solvents and supercritical carbon dioxide. / Capewell, A.; Wendel, V.; Bornscheuer, Uwe T. et al.
In: Enzyme and microbial technology, Vol. 19, No. 3, 15.08.1996, p. 181-186.

Research output: Contribution to journalArticleResearchpeer review

Capewell A, Wendel V, Bornscheuer UT, Meyer HH, Scheper T. Lipase-catalyzed kinetic resolution of 3-hydroxy esters in organic solvents and supercritical carbon dioxide. Enzyme and microbial technology. 1996 Aug 15;19(3):181-186. doi: 10.1016/0141-0229(95)00229-4
Capewell, A. ; Wendel, V. ; Bornscheuer, Uwe T. et al. / Lipase-catalyzed kinetic resolution of 3-hydroxy esters in organic solvents and supercritical carbon dioxide. In: Enzyme and microbial technology. 1996 ; Vol. 19, No. 3. pp. 181-186.
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abstract = "The lipase-catalyzed kinetic resolution of different 3-hydroxy esters in organic solvents and supercritical carbon dioxide (SCCO2) was studied. Similar enantiomeric excesses (ee, up to 99%) as found for transesterifications in organic solvents were achieved also in SCCO2. The influence of various reaction parameters was investigated for the resolution of 3-hydroxy octanoic acid methyl esters with lipase from Pseudomonas cepacia in SCCO2. Optimum conditions have been found at 11O bar, 40°C, and in the presence of 1.5 g molecular sieve by using vinyl acetate as acyl donor. The addition of different cosolvents had only a small effect on the reaction. Immobilization of the lipase on VA-epoxy resulted in similar optical purities as found for the elude lipase, but at halved reaction times. The effect of supercritical conditions on the stability of the lipase was also investigated.",
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AU - Capewell, A.

AU - Wendel, V.

AU - Bornscheuer, Uwe T.

AU - Meyer, H. H.

AU - Scheper, T.

N1 - Funding information: This work was financially supportedb y the EEC BRIDGE program (Grant BIOT-CT-90-0176). The authors are grateful to Merck (Darmstadt,G ermany) for kindly providing us with chemicals and Amano PharmaceuticalsL td., Nagoya, Japan for the gift of lipase.

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N2 - The lipase-catalyzed kinetic resolution of different 3-hydroxy esters in organic solvents and supercritical carbon dioxide (SCCO2) was studied. Similar enantiomeric excesses (ee, up to 99%) as found for transesterifications in organic solvents were achieved also in SCCO2. The influence of various reaction parameters was investigated for the resolution of 3-hydroxy octanoic acid methyl esters with lipase from Pseudomonas cepacia in SCCO2. Optimum conditions have been found at 11O bar, 40°C, and in the presence of 1.5 g molecular sieve by using vinyl acetate as acyl donor. The addition of different cosolvents had only a small effect on the reaction. Immobilization of the lipase on VA-epoxy resulted in similar optical purities as found for the elude lipase, but at halved reaction times. The effect of supercritical conditions on the stability of the lipase was also investigated.

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