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dc.contributor.author | Dyachenko, V. D. | |
dc.contributor.author | Karpov, E. N. | |
dc.date.accessioned | 2018-03-06T06:24:01Z | |
dc.date.accessioned | 2018-08-16T10:30:59Z | |
dc.date.available | 2018-03-06T06:24:01Z | |
dc.date.available | 2018-08-16T10:30:59Z | |
dc.date.issued | 2013-10-07 | |
dc.identifier.uri | http://dspace.ltsu.org//handle/123456789/1633 | |
dc.description.abstract | 4-Alkyl-6-amino-4-N3,N5-diaryl-2-thioxo-1,2,3,4-tetrahydropyridine-3,5-dicarboxamides were obtained via tandem synthesis involving the Knoevenagel reaction, Michael reaction and intramolecular condensation. Alkylation of the obtained dicarboxamides proceeds regioselectively at the S atom to form the corresponding thioethers. Structure of 6-allylsulfanyl-2-amino-4-isobutyl-N3,N5-di-m-tolyl-3,4-dihydropyridine-3,5-dicarboxamide was uniquely determined by XRD analysis. | ru_RU |
dc.language.iso | other | ru_RU |
dc.title | 4-Alkyl-6-amino-4-N3,N5-diaryl-2-thioxo-1,2,3,4- tetrahydropyridine-3,5-dicarboxamides: I. Tandem Synthesis and Alkylation. Molecular and Crystal Structure of 6-Allylsulfanyl-2-amino-4-isobutyl-N3,N5-di-m-tolyl-3,4- dihydropyridine-3,5-dicarboxamide. | ru_RU |
dc.type | Article | ru_RU |