The 1H and 13C NMR resonances of 19 tetracyclic acridinone derivatives were completely and unambiguously assigned by a combination of 1H-detected one-bond HMQC and long-range (two and three bonds) HMBC correlation experiments. 1H and 13C chemical shifts are also reported for the respective N -aryl b
1H and 13C chemical shifts of some tetracyclic and pentacyclic acridinone derivatives
β Scribed by J. P. Hanoun; S. Morel; V. Pique; J. P. Galy; R. Faure
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 89 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
Reference Data
and chemical shifts of some tetracyclic and 1H 13C pentacyclic acridinone derivatives
π SIMILAR VOLUMES
The 1 H and 13 C NMR resonances of 12 tetracyclic phenothiazine derivatives were completely and unequivocally assigned by the concerted application of 1 H-detected heteronuclear one-bond (gs-HMQC) and long-range (gs-HMBC) gradient selected correlation experiments. 1 H and 13 C chemical shifts are al
The complete assignment of the 1H and 13C NMR spectra of eight thienyl-substituted chromenes was achieved by the concerted application of homonuclear (gs-COSY), 1H-detected heteronuclear one-bond (gs-HMQC) and long-range (gs-HMBC) gradientselected correlation experiments.
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