## Abstract Aldehyde (δCH) and enolic (δOH) proton chemical shifts, the corresponding spin–spin coupling constants (__J__CH,OH) and the ^13^C chemical shifts (δC) have been measured for three cyclic β‐ketoaldehydes as a function of temperature. A tautomeric equilibrium has been shown to exist betwe
A proton and 13C NMR study of keto-enol tautomerism of some β-ketoamides
✍ Scribed by M.T. Barros; C.F.G.C. Geraldes; C.D. Maycock; M.I. Silva
- Book ID
- 103208614
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- English
- Weight
- 214 KB
- Volume
- 142
- Category
- Article
- ISSN
- 0022-2860
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