## Abstract ^13^C NMR data of nineteen coumarins, twelve of which bear a prenyl (isoprenoid) side‐chain at C‐3, are reported and compared with those of the C‐3 unsubstituted compounds. Unlike the linear isomers, no γ‐effect is observed in the corresponding angular derivatives; this is proposed as s
13C NMR of coumarins. III—Simple coumarins
✍ Scribed by F. A. Macias; G. M. Massanet; F. Rodríguez-Luis; J. Salvá
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 236 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
13C NMR data for several simple coumarins are reported. The ysvn effect of a 5-methoxy substituent on the C-4 chemical shift was observed and measured. The effects of an 8-iodo substituent on the chemical shifts of the carbons of the coumarinic skeleton are discussed.
📜 SIMILAR VOLUMES
## Abstract ^13^C NMR data for several linear furanocoumarins are reported. The β, γ~syn~ and δ effects of a 5‐oxygenated function on the coumarinic skeleton were measured. A spectroscopic criterion for distinguishing between C‐5 and C‐8 oxygenated, between C‐5 oxygenated, C‐8 alkylated and C‐5 alk
## Abstract The signal shifts caused by replacing the carbonyl oxygen by sulphur represent a valuable method of assignment of the ^13^C NMR signals in coumarins and furocoumarins substituted at the benzoic and furanoic rings.