Academic Journal

Enantioselective Partitioning of Racemic Ibuprofen in a Biphasic Recognition Chiral Extraction System

التفاصيل البيبلوغرافية
العنوان: Enantioselective Partitioning of Racemic Ibuprofen in a Biphasic Recognition Chiral Extraction System
المؤلفون: Tang, Kewen, Song, Litao, Pan, Yang, Jiang, Xinyu, Miao, Jiabing
المصدر: Chinese Journal of Chemistry ; volume 28, issue 1, page 119-124 ; ISSN 1001-604X 1614-7065
بيانات النشر: Wiley
سنة النشر: 2010
المجموعة: Wiley Online Library (Open Access Articles via Crossref)
الوصف: Enantioselective partitioning of ibuprofen enantiomers in a biphasic recognition chiral extraction system was studied. A combination of hydrophobic L ‐isobutyl tartrate in organic phase and hydrophilic β ‐cyclodextrin derivative in aqueous phase is necessary to establish a biphasic recognition chiral extraction system. The studies performed involve an enantioselective extraction in a biphasic system, where ibuprofen enantiomers form four complexes with the β ‐cyclodextrin derivative in aqueous phase and the D ( L )‐isobutyl tartrate in organic phase, respectively. In these biphasic resolutions, the types and the concentrations of the extractants, pH and temperature all exert a considerable influence on the biphasic recognition process. Good enantioselectivities for ibuprofen enantiomers were obtained at pH≦2.5 and a ratio of 2:1 of [ L ‐isobutyl tartrate] to [HP‐ β ‐CD]. Biphasic recognition chiral extraction is of strong chiral separation ability, and may be very helpful to optimize the extraction systems and realize the large‐scale production of enantiomers.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1002/cjoc.201090026
الاتاحة: http://dx.doi.org/10.1002/cjoc.201090026
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fcjoc.201090026
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.201090026
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رقم الانضمام: edsbas.E88B98E3
قاعدة البيانات: BASE