Chiral recognition with a benzofuran receptor that mimics an oxyanion holeElectronic supplementary information (ESI) available: Experimental procedures, 1H and 13C NMR, IR and HRMS spectra of compounds 1-8 and guests of Tables 2-4, modeling studies of Fig. 1 and 7 and X-ray diffraction data of compounds 6 and 7, determination of the absolute configuration of (+)-7 and (+)-8 by simulation of ECD spectra. CCDC 1010318-1010319. For ESI and crystallographic data in CIF or other electronic format see
A new chiral benzofuran receptor has been synthesized and its properties in the association of amino acid derivatives have been studied. X-ray structures were obtained and these corroborate the presence of an oxyanion-hole motif in these structures. Chiral resolution of a novel tripodal oxyanion-hol...
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| creator | Fuentes de Arriba, Ángel L Herrero, Ángel Gómez Rubio, Omayra H Monleón, Laura M Simón Rubio, Luis Alcázar, Victoria Sanz, Francisca Morán, Joaquín R |
| description | A new chiral benzofuran receptor has been synthesized and its properties in the association of amino acid derivatives have been studied. X-ray structures were obtained and these corroborate the presence of an oxyanion-hole motif in these structures.
Chiral resolution of a novel tripodal oxyanion-hole receptor with application in amino acid derivatives enantioselective extraction. |
| doi_str_mv | 10.1039/c4ob01954g |
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Chiral resolution of a novel tripodal oxyanion-hole receptor with application in amino acid derivatives enantioselective extraction.</abstract><doi>10.1039/c4ob01954g</doi><tpages>9</tpages></addata></record> |
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| source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
| title | Chiral recognition with a benzofuran receptor that mimics an oxyanion holeElectronic supplementary information (ESI) available: Experimental procedures, 1H and 13C NMR, IR and HRMS spectra of compounds 1-8 and guests of Tables 2-4, modeling studies of Fig. 1 and 7 and X-ray diffraction data of compounds 6 and 7, determination of the absolute configuration of (+)-7 and (+)-8 by simulation of ECD spectra. CCDC 1010318-1010319. For ESI and crystallographic data in CIF or other electronic format see |
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