1980
DOI: 10.1080/00387018008064055
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Configurational Structure of 1, 3-Indandione Derivatives by13C-Nuclear Magnetic Resonance

Abstract: 13C-NMR studies of certain 2-acyl-l , 3-indandiones indicate that the preferred tautomeric form is the enol structure and not the triketo structure. and 2-benzoyl-1,3-indandiones are discussed.The I'C-NMR spectral assignment of 2-propionyl Introduction:

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Cited by 3 publications
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“…It may be of interest that the same behaviour has been overlooked in the interpretation of the 13 C NMR data of 2-propionyl-l,3-indandione [21].…”
Section: Resultsmentioning
confidence: 98%
“…It may be of interest that the same behaviour has been overlooked in the interpretation of the 13 C NMR data of 2-propionyl-l,3-indandione [21].…”
Section: Resultsmentioning
confidence: 98%
“…Titration of 1-methylimidazoline-2-thione, a weak organic acid, with NaOH solution with conductometric determination of the equivalence point was described in [82]. This method can be used for routine assays at the quality control stage.…”
Section: Titrimetric and Electrotitrimetric Analysis Methodsmentioning
confidence: 99%
“…Further reaction of 6 with sodium azide in hot aqueous DMSO according to ref. [22] yielded 7, which was utilized to prepare the saturated compound 8 and the desired unsaturated derivatives 9, 10, and 11. Catalytic hydrogenation of 7 using palladium/charcoal followed by treatment with phthalic anhydride in acetic acid yielded 8.…”
Section: Chemistrymentioning
confidence: 99%