76 resultados para CHIRAL SYMMETRY-BREAKING
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- AMS Campus - Alm@DL - Università di Bologna (1)
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- ArchiMeD - Elektronische Publikationen der Universität Mainz - Alemanha (19)
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- Aston University Research Archive (31)
- Biblioteca Digital da Produção Intelectual da Universidade de São Paulo (30)
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- Doria (National Library of Finland DSpace Services) - National Library of Finland, Finland (3)
- Duke University (2)
- Institute of Public Health in Ireland, Ireland (1)
- Instituto Politécnico do Porto, Portugal (2)
- Iowa Publications Online (IPO) - State Library, State of Iowa (Iowa), United States (2)
- Lume - Repositório Digital da Universidade Federal do Rio Grande do Sul (2)
- Martin Luther Universitat Halle Wittenberg, Germany (3)
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- National Center for Biotechnology Information - NCBI (22)
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- Repositório Institucional UNESP - Universidade Estadual Paulista "Julio de Mesquita Filho" (258)
- RUN (Repositório da Universidade Nova de Lisboa) - FCT (Faculdade de Cienecias e Technologia), Universidade Nova de Lisboa (UNL), Portugal (6)
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- Universidad de Alicante (22)
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- Universidade Complutense de Madrid (6)
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- Universidade dos Açores - Portugal (1)
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- Universitätsbibliothek Kassel, Universität Kassel, Germany (3)
- Université de Lausanne, Switzerland (22)
- Université de Montréal, Canada (10)
- University of Connecticut - USA (1)
- University of Michigan (30)
- University of Queensland eSpace - Australia (28)
- University of Southampton, United Kingdom (1)
- University of Washington (2)
Resumo:
The enantiomers of sulfoxide proton pump inhibitors - omeprazole, lansoprazole, rabeprazole and Ro 18-5364 - were enantiomerically separated by liquid chromatography at multimilligram scale on a poly saccharide-based chiral stationary phase using normal and polar organic conditions as mobile phase. The values of the recovery and production rate were significant for each enantiomer; better results were achieved using a solid-phase injection system. However, this system was applied just for the enantionteric separation of omeprazole to demonstrate the applicability of this injection mode at milligram scale. The chiroptical characterization of the compounds was performed using a polarimeter and a circular dichroism detector. The higher enantiomeric purity obtained for the isolated enantiomers suggests that the methods here described should be considered as a simple and rapid way to obtain enantiomeric pure standards for analytical purpose. (C) 2007 Elsevier B.V. All rights reserved.