The structure of benzoyldimedone from X-ray diffraction analysis

被引：0
作者：
E. V. Borisov
A. I. Verenich
A. A. Govorova
A. S. Lyakhov
T. S. Khlebnikova
机构：
[1] National Academy of Sciences of Belarus,Institute of Bioorganic Chemistry
[2] Belarussian State University,Institute of Physicochemical Problems
来源：
Russian Chemical Bulletin | 2000年 / 49卷
关键词：
X-ray diffraction analysis; tautomerism; intramolecular hydrogen bond; β-diketones; β-triketones; conjugation; 2-benzoyl-5,5-dimethylcyclohexane-1,3-dione;
D O I：
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学科分类号：
摘要：
The structure of benzoyldimedone was established by X-ray diffraction analysis. The only tautomer was found. In this tautomer, the enol proton is covalently bound to the oxygen atom that is remote from the phenyl group. The role of steric and electronic factors in stabilization of the enol structure is analyzed. The geometric characteristics of the ring formed through an intramolecular hydrogen bond are discussed.
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页码：1068 / 1070
页数：2
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