Ontology type: schema:ScholarlyArticle
2012-12
AUTHORSA. I. Vas’kevich, N. M. Tsyzoryk, V. I. Staninets, E. B. Rusanov, M. V. Vovk
ABSTRACTN-Aryl-4-phenylbut-3-enamides reacted with arenesulfenyl chlorides in chloroform to give N,4-diaryl-3-arylsulfanyl-4-chlorobutanamides, whereas in acetic acid in the presence of lithium perchlorate N-[4-arylsulfanyl-5-phenyltetrahydrofuran-2-ylidene]arenaminium perchlorates were obtained. Reactions of arenesulfenyl chlorides with N,4-diarylbut-3-enamides having strong electron-donating groups in positions 3 and 4 of the N-aryl substituent afforded 5-aryl-4-arylsulfanyl-2,3,4,5-tetrahydro-1H-1-benzazepin-2-ones.
PAGES1536-1543
http://scigraph.springernature.com/pub.10.1134/s107042801212007x
DOIhttp://dx.doi.org/10.1134/s107042801212007x
DIMENSIONShttps://app.dimensions.ai/details/publication/pub.1015546484
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/2008/0202",
"inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/",
"name": "Atomic, Molecular, Nuclear, Particle and Plasma Physics",
"type": "DefinedTerm"
},
{
"id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/02",
"inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/",
"name": "Physical Sciences",
"type": "DefinedTerm"
}
],
"author": [
{
"affiliation": {
"alternateName": "Institute of Organic Chemistry",
"id": "https://www.grid.ac/institutes/grid.464621.3",
"name": [
"Institute of Organic Chemistry, National Academy of Sciences of Ukraine, ul. Murmanskaya 5, 02660, Kiev, Ukraine"
],
"type": "Organization"
},
"familyName": "Vas\u2019kevich",
"givenName": "A. I.",
"id": "sg:person.016422071357.41",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016422071357.41"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Institute of Organic Chemistry",
"id": "https://www.grid.ac/institutes/grid.464621.3",
"name": [
"Institute of Organic Chemistry, National Academy of Sciences of Ukraine, ul. Murmanskaya 5, 02660, Kiev, Ukraine"
],
"type": "Organization"
},
"familyName": "Tsyzoryk",
"givenName": "N. M.",
"id": "sg:person.012314525755.92",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012314525755.92"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Institute of Organic Chemistry",
"id": "https://www.grid.ac/institutes/grid.464621.3",
"name": [
"Institute of Organic Chemistry, National Academy of Sciences of Ukraine, ul. Murmanskaya 5, 02660, 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": "Institute of Organic Chemistry",
"id": "https://www.grid.ac/institutes/grid.464621.3",
"name": [
"Institute of Organic Chemistry, National Academy of Sciences of Ukraine, ul. Murmanskaya 5, 02660, Kiev, Ukraine"
],
"type": "Organization"
},
"familyName": "Rusanov",
"givenName": "E. B.",
"id": "sg:person.01247600537.28",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01247600537.28"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Institute of Organic Chemistry",
"id": "https://www.grid.ac/institutes/grid.464621.3",
"name": [
"Institute of Organic Chemistry, National Academy of Sciences of Ukraine, ul. Murmanskaya 5, 02660, Kiev, Ukraine"
],
"type": "Organization"
},
"familyName": "Vovk",
"givenName": "M. V.",
"id": "sg:person.013407403301.91",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013407403301.91"
],
"type": "Person"
}
],
"citation": [
{
"id": "sg:pub.10.1134/s1070428012020078",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1004271175",
"https://doi.org/10.1134/s1070428012020078"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1134/s1070428011080057",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1007170924",
"https://doi.org/10.1134/s1070428011080057"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1107/s0108767307043930",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1027786902"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1016/s0968-0896(01)00289-9",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1030820629"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1016/j.bmc.2006.05.070",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1032249808"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1016/s0040-4020(98)00698-x",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1032901493"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1016/s0968-0896(02)00616-8",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1038473903"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1016/s0968-0896(02)00616-8",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1038473903"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1177/107424840501000304",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1044886661"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1177/107424840501000304",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1044886661"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1021/jm000108p",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1055932437"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1021/jm000108p",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1055932437"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1021/jm00048a015",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1055933623"
],
"type": "CreativeWork"
}
],
"datePublished": "2012-12",
"datePublishedReg": "2012-12-01",
"description": "N-Aryl-4-phenylbut-3-enamides reacted with arenesulfenyl chlorides in chloroform to give N,4-diaryl-3-arylsulfanyl-4-chlorobutanamides, whereas in acetic acid in the presence of lithium perchlorate N-[4-arylsulfanyl-5-phenyltetrahydrofuran-2-ylidene]arenaminium perchlorates were obtained. Reactions of arenesulfenyl chlorides with N,4-diarylbut-3-enamides having strong electron-donating groups in positions 3 and 4 of the N-aryl substituent afforded 5-aryl-4-arylsulfanyl-2,3,4,5-tetrahydro-1H-1-benzazepin-2-ones.",
"genre": "research_article",
"id": "sg:pub.10.1134/s107042801212007x",
"inLanguage": [
"en"
],
"isAccessibleForFree": false,
"isPartOf": [
{
"id": "sg:journal.1136317",
"issn": [
"1070-4280",
"1608-3393"
],
"name": "Russian Journal of Organic Chemistry",
"type": "Periodical"
},
{
"issueNumber": "12",
"type": "PublicationIssue"
},
{
"type": "PublicationVolume",
"volumeNumber": "48"
}
],
"name": "Intramolecular electrophilic cyclization of functional derivatives of unsaturated compounds: III. Reaction of N,4-Diarylbut-3-enamides with arenesulfenyl chlorides. Synthesis of 5-aryl-4-arylsulfanyl-2,3,4,5-tetrahydro-1H-1-benzazepin-2-ones",
"pagination": "1536-1543",
"productId": [
{
"name": "readcube_id",
"type": "PropertyValue",
"value": [
"4a1222a48e1206c83717ca71bdb1a9606f5bfc5a6c4aecb3b488271d2e2102ff"
]
},
{
"name": "doi",
"type": "PropertyValue",
"value": [
"10.1134/s107042801212007x"
]
},
{
"name": "dimensions_id",
"type": "PropertyValue",
"value": [
"pub.1015546484"
]
}
],
"sameAs": [
"https://doi.org/10.1134/s107042801212007x",
"https://app.dimensions.ai/details/publication/pub.1015546484"
],
"sdDataset": "articles",
"sdDatePublished": "2019-04-10T23:22",
"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_8693_00000504.jsonl",
"type": "ScholarlyArticle",
"url": "http://link.springer.com/10.1134%2FS107042801212007X"
}
]
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.10.1134/s107042801212007x'
N-Triples is a line-based linked data format ideal for batch operations.
curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1134/s107042801212007x'
Turtle is a human-readable linked data format.
curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1134/s107042801212007x'
RDF/XML is a standard XML format for linked data.
curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1134/s107042801212007x'
This table displays all metadata directly associated to this object as RDF triples.
121 TRIPLES
21 PREDICATES
37 URIs
19 LITERALS
7 BLANK NODES