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- W2361877679 abstract "Studies on the stereoselective esterification reaction of racemic ibuprofen catalyzed by lipase in AOT/water/n-heptane microemulsion have been carried out by chiral HPLC.The results show that the esterification reactions between racemic ibuprofen and alcohols can carry on smoothly in the AOT microemulsion.The conversion rate is 0.3613 and the product is mainly S-isomer of ibuprofen n-octyl ester which enantiomeric excess value is 0.9732.The ω_0 value(the molar ratio of water to AOT) and the AOT concentration affect the esterification reaction conversion rate,while they have little effect on the enantiomeric excess value of the product.The alcohols with different chain lengths have effects not only on esterification reaction conversion rate and its optimum ω_0 value but also on the enantiomeric excess value of ibuprofen esters." @default.
- W2361877679 created "2016-06-24" @default.
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- W2361877679 date "2006-01-01" @default.
- W2361877679 modified "2023-09-25" @default.
- W2361877679 title "Study on separation of racemic iuprofen catalyzed by lipase in AOT/water/n-heptane microemulsion" @default.
- W2361877679 hasPublicationYear "2006" @default.
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