Ontology type: schema:ScholarlyArticle
2003-05
AUTHORSV. V. Orysyk, Yu. L. Zborovskii, V. I. Staninets, A. A. Dobosh, S. M. Khripak
ABSTRACTInteraction of potassium salts of quinazolin-2-thiol-4-one with γ-substituted allyl halides gave thiazoloquinazolinones with linear or angular structures depending on the structure of the carbonyl radical. S-Allyl substituted quinazolin-2-thiol-4-one reacted with halogens to give iminium salts of thiazinoquinazolinone with an angular structure. The conversion of these salts to the corresponding bases and thiazoloquinazolinones has been studied. More... »
PAGES640-644
http://scigraph.springernature.com/pub.10.1023/a:1025154317771
DOIhttp://dx.doi.org/10.1023/a:1025154317771
DIMENSIONShttps://app.dimensions.ai/details/publication/pub.1012839845
JSON-LD is the canonical representation for SciGraph data.
TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT
[
{
"@context": "https://springernature.github.io/scigraph/jsonld/sgcontext.json",
"about": [
{
"id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/0306",
"inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/",
"name": "Physical Chemistry (incl. Structural)",
"type": "DefinedTerm"
},
{
"id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/03",
"inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/",
"name": "Chemical Sciences",
"type": "DefinedTerm"
}
],
"author": [
{
"affiliation": {
"alternateName": "Uzhhorod National University",
"id": "https://www.grid.ac/institutes/grid.77512.36",
"name": [
"Uzhgorod State University, 88000, Uzhgorod, Ukraine"
],
"type": "Organization"
},
"familyName": "Orysyk",
"givenName": "V. V.",
"id": "sg:person.015771447007.77",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015771447007.77"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Institute of Organic Chemistry",
"id": "https://www.grid.ac/institutes/grid.464621.3",
"name": [
"National Academy of Sciences of Ukraine, Institute of Organic Chemistry, 02094, Kiev, Ukraine"
],
"type": "Organization"
},
"familyName": "Zborovskii",
"givenName": "Yu. L.",
"id": "sg:person.010120771367.48",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010120771367.48"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Institute of Organic Chemistry",
"id": "https://www.grid.ac/institutes/grid.464621.3",
"name": [
"National Academy of Sciences of Ukraine, Institute of Organic Chemistry, 02094, Kiev, Ukraine"
],
"type": "Organization"
},
"familyName": "Staninets",
"givenName": "V. I.",
"id": "sg:person.016653667731.06",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016653667731.06"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Uzhhorod National University",
"id": "https://www.grid.ac/institutes/grid.77512.36",
"name": [
"Uzhgorod State University, 88000, Uzhgorod, Ukraine"
],
"type": "Organization"
},
"familyName": "Dobosh",
"givenName": "A. A.",
"id": "sg:person.013465126233.59",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013465126233.59"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Uzhhorod National University",
"id": "https://www.grid.ac/institutes/grid.77512.36",
"name": [
"Uzhgorod State University, 88000, Uzhgorod, Ukraine"
],
"type": "Organization"
},
"familyName": "Khripak",
"givenName": "S. M.",
"id": "sg:person.014073046243.68",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014073046243.68"
],
"type": "Person"
}
],
"citation": [
{
"id": "https://doi.org/10.1002/jhet.5570270552",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1002228538"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1002/jhet.5570270552",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1002228538"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1002/ardp.19833160617",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1017305955"
],
"type": "CreativeWork"
}
],
"datePublished": "2003-05",
"datePublishedReg": "2003-05-01",
"description": "Interaction of potassium salts of quinazolin-2-thiol-4-one with \u03b3-substituted allyl halides gave thiazoloquinazolinones with linear or angular structures depending on the structure of the carbonyl radical. S-Allyl substituted quinazolin-2-thiol-4-one reacted with halogens to give iminium salts of thiazinoquinazolinone with an angular structure. The conversion of these salts to the corresponding bases and thiazoloquinazolinones has been studied.",
"genre": "research_article",
"id": "sg:pub.10.1023/a:1025154317771",
"inLanguage": [
"en"
],
"isAccessibleForFree": false,
"isPartOf": [
{
"id": "sg:journal.1356886",
"issn": [
"0009-3122",
"1573-8353"
],
"name": "Chemistry of Heterocyclic Compounds",
"type": "Periodical"
},
{
"issueNumber": "5",
"type": "PublicationIssue"
},
{
"type": "PublicationVolume",
"volumeNumber": "39"
}
],
"name": "Synthesis of Thiazino- and Thiazoloquinazolinones by Cyclization of S-(2-Propenyl) Derivatives of 2-Thioxo-2,3-dihydro-4(1H)-quinazolinone",
"pagination": "640-644",
"productId": [
{
"name": "readcube_id",
"type": "PropertyValue",
"value": [
"3d2abfa191bae80dd9e688fdaae72e67a4ca913d260b62ad94f7c7331532089d"
]
},
{
"name": "doi",
"type": "PropertyValue",
"value": [
"10.1023/a:1025154317771"
]
},
{
"name": "dimensions_id",
"type": "PropertyValue",
"value": [
"pub.1012839845"
]
}
],
"sameAs": [
"https://doi.org/10.1023/a:1025154317771",
"https://app.dimensions.ai/details/publication/pub.1012839845"
],
"sdDataset": "articles",
"sdDatePublished": "2019-04-10T19:55",
"sdLicense": "https://scigraph.springernature.com/explorer/license/",
"sdPublisher": {
"name": "Springer Nature - SN SciGraph project",
"type": "Organization"
},
"sdSource": "s3://com-uberresearch-data-dimensions-target-20181106-alternative/cleanup/v134/2549eaecd7973599484d7c17b260dba0a4ecb94b/merge/v9/a6c9fde33151104705d4d7ff012ea9563521a3ce/jats-lookup/v90/0000000001_0000000264/records_8681_00000504.jsonl",
"type": "ScholarlyArticle",
"url": "http://link.springer.com/10.1023%2FA%3A1025154317771"
}
]Download the RDF metadata as: json-ld nt turtle xml License info
JSON-LD is a popular format for linked data which is fully compatible with JSON.
curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/pub.10.1023/a:1025154317771'
N-Triples is a line-based linked data format ideal for batch operations.
curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1023/a:1025154317771'
Turtle is a human-readable linked data format.
curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1023/a:1025154317771'
RDF/XML is a standard XML format for linked data.
curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1023/a:1025154317771'
This table displays all metadata directly associated to this object as RDF triples.
98 TRIPLES
21 PREDICATES
29 URIs
19 LITERALS
7 BLANK NODES