## Abstract The ^13^C NMR spectra of 1‐aryl‐substituted 3‐methyl‐2‐pyrazolin‐5‐ones and their azomethine dyes have been recorded and assigned. __ortho__‐Substituents (Cl and NO~2~) on the phenyl ring in the 1‐position of the pyrazoline moiety show a small influence on the chemical shift of the azom
13C NMR data for 7- and/or 9-aza-substituted naphthalenecyclolignans
✍ Scribed by M. Angeles Castro; José M. Miguel del Corral; M. Luisa López-Vázquez; Pablo A. García; Arturo San Feliciano; Marina Gordaliza
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 265 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Eight thia-or aza-substituted butyric acid derivatives were prepared and the influence of these substituents on aromatic 13 C NMR shifts was studied.
## Abstract In this article we present a complete ^1^H and ^13^C NMR spectral analysis of three 7,7′‐dihydroarylnaphthalene lignan lactones using modern NMR techniques such as COSY, HSQC, HMBC and NOE experiments. Complete assignment and homonuclear hydrogen coupling constant measurements were perf
## Abstract The ^1^H and ^13^C NMR spectra of 3‐azabicyclo[3.3.1]nonanes with various oxygenated substituents at C‐6 were assigned using 1D (DEPT) and 2D (COSY, HSQC, HMBC, NOESY) experiments. Close examination of this NMR data details the effects of substitution and stereochemistry at C‐6 in these
## Abstract The ^13^C NMR spectra of 26 substituted 2‐azabicyclo[3.3.1]nonan‐7‐ones are reported, providing a diagnostic method for the stereochemical elucidation of the relative configuration of these products.