Formation of N&ndash;S Bonds in Reactions of 2-[2-Oxo-1-(tosyloxyimino)-2-phenylethyl]pyrimidin-4(3H)-one and Its 6-derivatives with Thiourea and Potassium Thiocyanate

Yavolovskii Arkadii; Ivanov Iu.; Grishchuk L.; Kravtsov Victor; Fonari Marina; Kamalov Gerbert

Conţinutul numărului revistei

Articolul precedent

Articolul urmator

679

SM ISO690:2012

YAVOLOVSKII, Arkadii, IVANOV, Iu., GRISHCHUK, L., KRAVTSOV, Victor, FONARI, Marina, KAMALOV, Gerbert. Formation of N–S Bonds in Reactions of 2-[2-Oxo-1-(tosyloxyimino)-2-phenylethyl]pyrimidin-4(3H)-one and Its 6-derivatives with Thiourea and Potassium Thiocyanate. In: Russian Journal of Organic Chemistry, 2018, nr. 8(54), pp. 1213-1217. ISSN 1070-4280. DOI: https://doi.org/10.1134/S1070428018080158

EXPORT metadate:
Google Scholar
Crossref
CERIF

DataCite
Dublin Core

Russian Journal of Organic Chemistry

Numărul 8(54) / 2018 / ISSN 1070-4280

Formation of N–S Bonds in Reactions of 2-[2-Oxo-1-(tosyloxyimino)-2-phenylethyl]pyrimidin-4(3H)-one and Its 6-derivatives with Thiourea and Potassium Thiocyanate

DOI:https://doi.org/10.1134/S1070428018080158

Pag. 1213-1217

Yavolovskii Arkadii¹, Ivanov Iu.¹, Grishchuk L.¹, Kravtsov Victor², Fonari Marina², Kamalov Gerbert¹

¹ A.V. Bogatsky Physico-Chemical Institute of the NAS of Ukraine,
² Institute of Applied Physics

Disponibil în IBN: 7 decembrie 2018

Rezumat

Reaction of potassium thiocyanate with 2-[2-oxo-1-(1-tosyloxyimino)-2-phenylethyl]pyrimidin-4-(3H)-one derivatives led to the formation of a new fused heterocyclic system with a common nitrogen atom, substituted 7H-[1,2,5]thiadiazolo[2,3-a]pyrimidin-7-one.

Cerif XML Export

<?xml version='1.0' encoding='utf-8'?>
<CERIF xmlns='urn:xmlns:org:eurocris:cerif-1.5-1' xsi:schemaLocation='urn:xmlns:org:eurocris:cerif-1.5-1 http://www.eurocris.org/Uploads/Web%20pages/CERIF-1.5/CERIF_1.5_1.xsd' xmlns:xsi='http://www.w3.org/2001/XMLSchema-instance' release='1.5' date='2012-10-07' sourceDatabase='Output Profile'>
<cfResPubl>
<cfResPublId>ibn-ResPubl-68910</cfResPublId>
<cfResPublDate>2018-08-01</cfResPublDate>
<cfVol>54</cfVol>
<cfIssue>8</cfIssue>
<cfStartPage>1213</cfStartPage>
<cfISSN>1070-4280</cfISSN>
<cfURI>https://ibn.idsi.md/ro/vizualizare_articol/68910</cfURI>
<cfTitle cfLangCode='EN' cfTrans='o'>Formation of N&ndash;S Bonds in Reactions of 2-[2-Oxo-1-(tosyloxyimino)-2-phenylethyl]pyrimidin-4(3H)-one and Its 6-derivatives with Thiourea and Potassium Thiocyanate</cfTitle>
<cfAbstr cfLangCode='EN' cfTrans='o'><p>Reaction of potassium thiocyanate with 2-[2-oxo-1-(1-tosyloxyimino)-2-phenylethyl]pyrimidin-4-(3H)-one derivatives led to the formation of a new fused heterocyclic system with a common nitrogen atom, substituted 7H-[1,2,5]thiadiazolo[2,3-a]pyrimidin-7-one.</p></cfAbstr>
<cfResPubl_Class>
<cfClassId>eda2d9e9-34c5-11e1-b86c-0800200c9a66</cfClassId>
<cfClassSchemeId>759af938-34ae-11e1-b86c-0800200c9a66</cfClassSchemeId>
<cfStartDate>2018-08-01T24:00:00</cfStartDate>
</cfResPubl_Class>
<cfResPubl_Class>
<cfClassId>e601872f-4b7e-4d88-929f-7df027b226c9</cfClassId>
<cfClassSchemeId>40e90e2f-446d-460a-98e5-5dce57550c48</cfClassSchemeId>
<cfStartDate>2018-08-01T24:00:00</cfStartDate>
</cfResPubl_Class>
<cfPers_ResPubl>
<cfPersId>ibn-person-22084</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2018-08-01T24:00:00</cfStartDate>
</cfPers_ResPubl>
<cfPers_ResPubl>
<cfPersId>ibn-person-21990</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2018-08-01T24:00:00</cfStartDate>
</cfPers_ResPubl>
<cfPers_ResPubl>
<cfPersId>ibn-person-63382</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2018-08-01T24:00:00</cfStartDate>
</cfPers_ResPubl>
<cfPers_ResPubl>
<cfPersId>ibn-person-1035</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2018-08-01T24:00:00</cfStartDate>
</cfPers_ResPubl>
<cfPers_ResPubl>
<cfPersId>ibn-person-1018</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2018-08-01T24:00:00</cfStartDate>
</cfPers_ResPubl>
<cfPers_ResPubl>
<cfPersId>ibn-person-15980</cfPersId>
<cfClassId>49815870-1cfe-11e1-8bc2-0800200c9a66</cfClassId>
<cfClassSchemeId>b7135ad0-1d00-11e1-8bc2-0800200c9a66</cfClassSchemeId>
<cfStartDate>2018-08-01T24:00:00</cfStartDate>
</cfPers_ResPubl>
<cfFedId>
<cfFedIdId>ibn-doi-68910</cfFedIdId>
<cfFedId>10.1134/S1070428018080158</cfFedId>
<cfStartDate>2018-08-01T24:00:00</cfStartDate>
<cfFedId_Class>
<cfClassId>31d222b4-11e0-434b-b5ae-088119c51189</cfClassId>
<cfClassSchemeId>bccb3266-689d-4740-a039-c96594b4d916</cfClassSchemeId>
</cfFedId_Class>
<cfFedId_Srv>
<cfSrvId>5123451</cfSrvId>
<cfClassId>eda2b2e2-34c5-11e1-b86c-0800200c9a66</cfClassId>
<cfClassSchemeId>5a270628-f593-4ff4-a44a-95660c76e182</cfClassSchemeId>
</cfFedId_Srv>
</cfFedId>
</cfResPubl>
<cfPers>
<cfPersId>ibn-Pers-22084</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-22084-3</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2018-08-01T24:00:00</cfStartDate>
<cfFamilyNames>Yavolovskii</cfFamilyNames>
<cfFirstNames>Arkadii</cfFirstNames>
</cfPersName_Pers>
</cfPers>
<cfPers>
<cfPersId>ibn-Pers-21990</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-21990-3</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2018-08-01T24:00:00</cfStartDate>
<cfFamilyNames>Иванов </cfFamilyNames>
<cfFirstNames>И.</cfFirstNames>
</cfPersName_Pers>
</cfPers>
<cfPers>
<cfPersId>ibn-Pers-63382</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-63382-3</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2018-08-01T24:00:00</cfStartDate>
<cfFamilyNames>Grishchuk</cfFamilyNames>
<cfFirstNames>L.</cfFirstNames>
</cfPersName_Pers>
</cfPers>
<cfPers>
<cfPersId>ibn-Pers-1035</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-1035-3</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2018-08-01T24:00:00</cfStartDate>
<cfFamilyNames>Kravtsov</cfFamilyNames>
<cfFirstNames>Victor</cfFirstNames>
<cfFamilyNames>Кравцов</cfFamilyNames>
<cfFirstNames>Виктор</cfFirstNames>
</cfPersName_Pers>
</cfPers>
<cfPers>
<cfPersId>ibn-Pers-1018</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-1018-3</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2018-08-01T24:00:00</cfStartDate>
<cfFamilyNames>Fonari</cfFamilyNames>
<cfFirstNames>Marina</cfFirstNames>
</cfPersName_Pers>
</cfPers>
<cfPers>
<cfPersId>ibn-Pers-15980</cfPersId>
<cfPersName_Pers>
<cfPersNameId>ibn-PersName-15980-3</cfPersNameId>
<cfClassId>55f90543-d631-42eb-8d47-d8d9266cbb26</cfClassId>
<cfClassSchemeId>7375609d-cfa6-45ce-a803-75de69abe21f</cfClassSchemeId>
<cfStartDate>2018-08-01T24:00:00</cfStartDate>
<cfFamilyNames>Kamalov</cfFamilyNames>
<cfFirstNames>Gerbert</cfFirstNames>
<cfFamilyNames>Камалов</cfFamilyNames>
<cfFirstNames>Герберт</cfFirstNames>
<cfFamilyNames>Камалов</cfFamilyNames>
<cfFirstNames>Герберт</cfFirstNames>
</cfPersName_Pers>
</cfPers>
<cfSrv>
<cfSrvId>5123451</cfSrvId>
<cfName cfLangCode='en' cfTrans='o'>CrossRef DOI prefix service</cfName>
<cfDescr cfLangCode='en' cfTrans='o'>The service of issuing DOI prefixes to publishers</cfDescr>
<cfKeyw cfLangCode='en' cfTrans='o'>persistent identifier; Digital Object Identifier</cfKeyw>
</cfSrv>
</CERIF>