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An investigation of the keto-enol tautomerism in 2-acetyl-1-tetralone by 2D NMR spectroscopy

✍ Scribed by Pawan K. Agrawal; Raghunath S. Thakur; August W. Frahm; M. Schneider

Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
233 KB
Volume
28
Category
Article
ISSN
0749-1581

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✦ Synopsis

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.

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