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 |
|