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Original scientific paper

MNDO Study of Tautomerism in 3-Acetyltetramic Acid

Mirjana Eckert-Maksić ; Department of Organic Chemistry and Biochemistry, »Rudjer Bošković" Institute, 41001 Zagreb, Croatia, Yugoslavia
Ljiljana Maksimović ; Department of Organic Chemistry and Biochemistry, »Rudjer Bošković" Institute, 41001 Zagreb, Croatia, Yugoslavia


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Abstract

The tautomerism of 3-acetyltetramic acid was investigated by using the semiempirical MNDO method. Calculations predict that the exo-enol tautomers (B and D) are more stable than the endo-enol forms (A and Cl. The estimated !1Hr's are -473.7, -475.2, -457.5 and -453.4 kjoule mol:", respectively. Lactim tautomers A' and B' are found to be by ca. 22 kjoule mol? less stable than the corresponding lactam tautomers A and B. The origtn of relative stabilities of tautomers is elucidated by the energy partitioning technique.

Keywords

Hrčak ID:

177303

URI

https://hrcak.srce.hr/177303

Publication date:

25.7.1986.

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