## 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
Preparation of 3-(Trifluoromethyl)coumarins
✍ Scribed by Wojciech Dmowski; Krystyna Piasecka-Maciejewska
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 28 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
Previously difficult to prepare, aliphatic and alicyclic trifluoromethylketones (e.g. 1 and 2), which are of pharmacalogic interest as potential enzyme inhibitors, can now be synthesized easily and efficiently. The one-step reaction starting with carbonic esters and trimethyl(trifluoromethyl)silane
## Abstract 3‐Acetylcoumarine was condensed with dimethylformamide dimethylacetal (DMFDMA) to yield the enaminone, which reacts readily with hydroxylamine and with hydrazines to yield coumarin‐3‐ylisoxazoles and coumarin‐3‐ylpyrazoles respectively. Reaction of the enaminone with benzamidine hydroch