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NMR and theoretical investigation of the keto–enol tautomerism in cyclohexane-1,3-diones

✍ Scribed by Valdemar Lacerda Júnior; Mauricio G. Constantino; Gil Valdo J. da Silva; Álvaro Cunha Neto; Cláudio F. Tormena


Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
149 KB
Volume
828
Category
Article
ISSN
0022-2860

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An investigation of the keto-enol tautom
✍ Pawan K. Agrawal; Raghunath S. Thakur; August W. Frahm; M. Schneider 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 233 KB

## Abstract Long‐range CH correlation and long‐range selective proton decoupling (LRSPD), together with other standard NMR techniques, led to the complete ^13^C and ^1^H NMR spectral assignments of 2‐acetyl‐1‐tetralone and demonstrated its existence in the __endo__‐enolic form.