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An n.m.r. study of keto?enol tautomerism in ?-diketones

✍ Scribed by Allen, Geoffrey; Dwek, Raymond A.


Book ID
120173101
Publisher
Royal Society of Chemistry
Year
1966
Weight
381 KB
Volume
0
Category
Article
ISSN
0045-6470

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N.m.r. studies of the keto–enol tautomer
✍ G. Klose; E. Ludwig; E. Uhlemann πŸ“‚ Article πŸ“… 1977 πŸ› John Wiley and Sons 🌐 English βš– 522 KB

## Abstract Acetylthioacetamides exist as different keto and enol isomers in chloroform solutions. The keto form with intramolecular hydrogen bonding between the NH and the carbonyl group is the dominant keto isomer. On the other hand the enol forms with intramolecular hydrogen bonding between the