NMR and conformational studies of new 5-phenylpyrrole-carboxamide derivatives
The 1H and 13C NMR resonances of 22 5‐(5‐substituted‐2‐nitrophenyl)‐1H‐pyrrole‐2‐carboxamides, 22 5‐(5‐substituted‐2‐aminophenyl)‐1H‐pyrrole‐2‐carboxamides, and 9 5‐phenyl‐1H‐pyrrole‐2‐carboxamides were assigned completely using the concerted application of one‐ and two‐dimensional experiments (DEPT...
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Veröffentlicht in: | Magnetic resonance in chemistry 2009-12, Vol.47 (12), p.1101-1109 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The 1H and 13C NMR resonances of 22 5‐(5‐substituted‐2‐nitrophenyl)‐1H‐pyrrole‐2‐carboxamides, 22 5‐(5‐substituted‐2‐aminophenyl)‐1H‐pyrrole‐2‐carboxamides, and 9 5‐phenyl‐1H‐pyrrole‐2‐carboxamides were assigned completely using the concerted application of one‐ and two‐dimensional experiments (DEPT, gs‐HMQC and gs‐HMBC). NOE studies and conformational analysis confirm the preferred conformations of such compounds. Copyright © 2009 John Wiley & Sons, Ltd.
The 1H and 13C NMR resonances of 53 5‐(2,5‐disubstitutedphenyl)‐1H‐pyrrole‐2‐carboxamides were assigned completely. NOE studies and conformational analysis confirm the preferred conformation of such compounds. |
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ISSN: | 0749-1581 1097-458X 1097-458X |
DOI: | 10.1002/mrc.2524 |