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Study of Enol-Keto Tautomerism of N-(2-Hydroxy-1-Naphthylidene)anils

✍ Scribed by Nagy, Pál; Herzfeld, Rozália

Book ID
127140658
Publisher
Taylor and Francis Group
Year
1998
Tongue
English
Weight
333 KB
Volume
31
Category
Article
ISSN
0038-7010

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## 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