Heterocumulenes reactions with organometallic reagents: XX. Quantum-chemical study of concurrent processes of structural reorganization of N-Methyl-2-methoxy- and 2-(methylsulfanyl)buta-2,3-dienimidothioates into pyrroles and/or 2,3-dihydropyridines |
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Authors: | V A Shagun N A Hedolya |
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Institution: | 1. Faworsky Irkutsk Institute of Chemistry, Siberian Branch of Russian Academy of Sciences, Irkutsk, 664033, Russia
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Abstract: | Utilizing the MP2/6-31G(d,p) method a quantum-chemical investigation was performed of thermally induced formation of pyrrole and/or 2,3-dihydropyridine structures from methyl N-methyl-2-methoxy- and 2-(methylsulfanyl)buta-2,3-dienimidothioates (1-aza-1,3,4-trienes). According to calculations the pyrrole and dihydropyridine cyclization of a methoxy-substituted 1-aza-1,3,4-triene is both kinetically and thermodynamically virtually equally probable with a little prevalence of the first pathway. The main direction of the structural reorganization of methylsulfanyl-substituted 1-aza-1,3,4-triene is the kinetically controlled formation of the dihydropyridine ring. |
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