Synthesis of 2-(1-Alkoxyvinyl)oxazolidines by Condensation of 2-Alkoxypropenals with 2-Aminoalkanols and Ring—Chain Tautomerism of the Products.
✍ Scribed by N. A. Keiko; E. A. Funtikova; L. G. Stepanova; Yu. A. Chuvashev; L. I. Larina
- Publisher
- John Wiley and Sons
- Year
- 2004
- Weight
- 155 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
Thiohydrazide compounds 1 react with lactam acetals 2 or solution, however, most of them undergo a reversible ringlactim ethers 3 by condensation giving unusual zwitterionic chain transformation to novel 2-(o-aminoalkyl)-1,3,4-thiaditautomers 5 of lactam thioacylhydrazones 4. These compounds azole s
## Abstract magnified image The condensation products of 2‐aminoethanol or 3‐aminopropanol (bearing an alkyl substituent on the carbon adjacent to the nitrogen) with substituted benzaldehydes proved to exist in CDCl~3~ at 300 K as threecomponent tautomeric mixtures of the diastereomeric five‐ or s