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Theoretical study on the mechanism of stable phosphorus ylides derived from 5-aminoindazole in the presence of different dialkyl acetyelenedicarboxylates | ||
| Iranian chemical communication | ||
| مقاله 9، دوره 5، Issue 3, pp. 237-363, Serial No. 16، مهر 2017، صفحه 301-307 اصل مقاله (784.05 K) | ||
| نوع مقاله: Original Research Article | ||
| نویسندگان | ||
| Mohammad Zakarianezhad* ؛ Motahare Shool | ||
| Payam Noor University | ||
| چکیده | ||
| In the recent work, the reaction mechanism between triphenylphosphine 1, dialkyl acetylenedicarboxylates 2 in the presence of NH-acid, such as 5-aminoindazole 3 were investigated theoretically. Quantum mechanical studies were performed for evaluation of potential energy surfaces of all structures participated in the reaction mechanism both in gas phase and in dichloromethane. The first step of all reactions was recognized as a rate-determining step in the reaction mechanism. All the possible structures partipated on the reaction coordinate were well predicted. Quantum mechanical calculations were clarified how the ylides exist in solution as a mixture of two geometrical isomers (Z- and E-) as a minor or major forms. | ||
| کلیدواژهها | ||
| NH-acid؛ theoretical study؛ Z- and E-rotamers؛ 5-aminoindazole؛ triphenylphosphine | ||
| مراجع | ||
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