The 1H and 13C NMR resonances of four 3H-naphtho[2,1-b]pyrans were completely and unambiguously assigned by a combination of homonuclear (gs-COSY), 1H-detected heteronuclear one-bond (gs-HMQC) and long-range (gs-HMBC) gradient-selected correlation experiments.
Complete assignment of the 1H and 13C NMR spectra of 2-phenyl-3H-naphtho[2,1-b][1,4]oxazin-3-one, 2-p-methoxyphenylnaphtho[1,2-d]oxazole and 2-phenylnaphtho[1,2-d]oxazole. Concerted use of one- and two-dimensional NMR techniques
✍ Scribed by Amelia Márquez; Claudio Saitz; Alvaro Cañete; Hernán Rodríguez; Carolina Jullian
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 223 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The 1H and 13C NMR spectra of 2-phenyl-3H-naphtho [2,1-b][1,4]oxazin-3-one, 2-p-methoxyphenylnaphtho [1,2-d]oxazole and 2-phenylnaphtho[1,2-d]oxazole were totally assigned using a combination of one-and two-dimensional NMR techniques. In addition to correlation of the proton signals by a COSY spectrum and one-bond heteronuclear correlation, complete assignment of the 1H and 13C NMR spectra of these heterocyclic compounds required the application of long-range CH coupling information, particularly for quaternary resonance assignments and for orientations of individual spin systems relative to one another.
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