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TADDOL organophosphorus derivatising agents for the determination of the enantiomeric excess of chiral alcohols and carboxylic acids by 31P and 1H NMR spectroscopy
Affiliation:1. LCME, FST Marrakech, Cadi Ayyad University, BP549, Avenue A. Khattabi, Marrakech, Morocco;2. Jülich Centre for Neutron Science, JCNS, and Peter Grünberg Institut PGI, JARA-FIT, Forschungszentrum Jülich GmbH, D-52425 Jülich, Germany;3. Center for Advanced Materials, Université Mohammed VI Polytechnique, Lot 660-Hay Moulay Rachid, Ben Guerir, Morocco;4. Institut Charles Gerhardt, UMR 5253 CNRS, Université de Montpellier, Place Eugène Bataillon, 34095 Montpellier cedex 5, France;5. Réseau sur le Stockage Electrochimique de l’Energie (RS2E), FR CNRS 3459, France;6. Faculté des Sciences, Université de Liège, B-4000 Liège, Belgium;7. Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA;1. Department of Applied Chemistry, Kyungpook National University, Daegu 702-701, Republic of Korea;2. Department of Environmental Engineering, Kyungpook National University, Daegu 702-701, Republic of Korea;1. Department of Chemistry, Faculty of Sciences, TarbiatModares University, Tehran, Iran;2. Institute of Physics of the ASCR, v.v.i., Na Slovance 2, 182 21 Praha 8, Czech Republic
Abstract:
The use of an organophosphorus derivatisation agent prepared from TADDOL for the NMR determination of enantiomeric composition of chiral alcohols and carboxylic acids is described.
Keywords:
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