Gated Decoupling 13C NMR Application to Determine Conformation and Unambiguous Chemical Shift of Arylidene Barbiturates

Verfasser / Beitragende:
[José Figueroa-Villar]
Ort, Verlag, Jahr:
2015
Enthalten in:
Applied Magnetic Resonance, 46/6(2015-06-01), 607-621
Format:
Artikel (online)
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024 7 0 |a 10.1007/s00723-015-0666-3  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00723-015-0666-3 
100 1 |a Figueroa-Villar  |D José  |u Medicinal Chemistry Group, Department of Chemistry, Military Institute of Engineering, Praça General Tibúrcio 80, Urca, 22290-270, Rio de Janeiro, RJ, Brazil  |4 aut 
245 1 0 |a Gated Decoupling 13C NMR Application to Determine Conformation and Unambiguous Chemical Shift of Arylidene Barbiturates  |h [Elektronische Daten]  |c [José Figueroa-Villar] 
520 3 |a Chemical shift assignment and conformational structure of small molecules are fundamental for their study of interaction with biological targets, like proteins and nucleic acids. Chemical shift assignments are usually obtained with the very efficient nuclear magnetic resonance (NMR) methods COSY, HSQC, HMBC, TOCSY and NOESY. When these NMR methods do not afford all information or need the results confirmation to determine the complete molecular chemical shift assignment, it is necessary to use other procedures, especially for determination of long range 1H-13C coupling constants and 13C multiplicity. In this work, it is demonstrated that Gated decoupling 13C NMR spectrum, which is a simple and easy to use method, is very appropriate to complete the unambiguous chemical shift assignment and the conformational condition of arylidene barbiturates. The NMR conformational results were also confirmed by molecular modeling. 
540 |a Springer-Verlag Wien, 2015 
773 0 |t Applied Magnetic Resonance  |d Springer Vienna  |g 46/6(2015-06-01), 607-621  |x 0937-9347  |q 46:6<607  |1 2015  |2 46  |o 723 
856 4 0 |u https://doi.org/10.1007/s00723-015-0666-3  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00723-015-0666-3  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 100  |E 1-  |a Figueroa-Villar  |D José  |u Medicinal Chemistry Group, Department of Chemistry, Military Institute of Engineering, Praça General Tibúrcio 80, Urca, 22290-270, Rio de Janeiro, RJ, Brazil  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Applied Magnetic Resonance  |d Springer Vienna  |g 46/6(2015-06-01), 607-621  |x 0937-9347  |q 46:6<607  |1 2015  |2 46  |o 723