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dc.contributor.author | Metlushka K. | |
dc.contributor.author | Sadkova D. | |
dc.contributor.author | Nikitina K. | |
dc.contributor.author | Lodochnikova O. | |
dc.contributor.author | Kataeva O. | |
dc.contributor.author | Alfonsov V. | |
dc.date.accessioned | 2018-04-05T07:09:39Z | |
dc.date.available | 2018-04-05T07:09:39Z | |
dc.date.issued | 2017 | |
dc.identifier.issn | 1070-3632 | |
dc.identifier.uri | http://dspace.kpfu.ru/xmlui/handle/net/129885 | |
dc.description.abstract | © 2017, Pleiades Publishing, Ltd. Phosphorylation of a naphthol hydroxy group of thiophosphorylated thiourea obtained by reaction of diethyl thiophosphoryl isothiocyanate with 1-(α-aminobenzyl)-2-naphthol (Betti base) afforded a number of chiral bisphosphorylated thioureas. Molecular structure of the obtained compounds was studied by single crystal X-ray diffraction. The capacity of the studied compounds for dimerization due to the intermolecular N–HS hydrogen bonding was revealed. | |
dc.relation.ispartofseries | Russian Journal of General Chemistry | |
dc.subject | Betti base | |
dc.subject | intra- and intermolecular interactions | |
dc.subject | O-phosphorylation | |
dc.subject | packing polymorphism | |
dc.subject | thiophosphorylated thioureas | |
dc.title | Betti base in the synthesis of chiral bisphosphorylated thioureas | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 9 | |
dc.relation.ispartofseries-volume | 87 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 1893 | |
dc.source.id | SCOPUS10703632-2017-87-9-SID85031938187 |