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dc.contributor.author | Kibardina L. | |
dc.contributor.author | Trifonov A. | |
dc.contributor.author | Bagautdinova R. | |
dc.contributor.author | Dobrynin A. | |
dc.contributor.author | Pudovik E. | |
dc.contributor.author | Burilov A. | |
dc.contributor.author | Pudovik M. | |
dc.date.accessioned | 2018-09-19T21:00:28Z | |
dc.date.available | 2018-09-19T21:00:28Z | |
dc.date.issued | 2016 | |
dc.identifier.issn | 1070-3632 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/143503 | |
dc.description.abstract | © 2016, Pleiades Publishing, Ltd.Interaction of pyridoxal (3-hydroxy-5-hydroxymethyl-2-methylisonicotinaldehyde) with amines, mono- and disubstituted diamines led to the formation of compounds having in their structure imine, imidazolidine, and pyrimidine moieties. Structure of the obtained compounds was proved by IR data, 1H NMR spectroscopy, mass spectrometry, and X-ray diffraction analysis. | |
dc.relation.ispartofseries | Russian Journal of General Chemistry | |
dc.subject | aliphatic diamines | |
dc.subject | amines | |
dc.subject | pyridoxal | |
dc.subject | pyridoxalimidazolidines | |
dc.subject | pyridoxalimines | |
dc.title | Pyridoxal reactions with amines and aliphatic diamines | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 3 | |
dc.relation.ispartofseries-volume | 86 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 607 | |
dc.source.id | SCOPUS10703632-2016-86-3-SID84969700110 |