5-Aryl-1,3,4-oxadiazoline-2(3H)-thiones in reactions with alkyl haloacetates View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2012-06

AUTHORS

A. A. Ziyaev, I. F. Tozhiev, Kh. M. Shakhidoyatov

ABSTRACT

The reaction of 5-aryl-1,3,4-oxadiazoline-2(3H)-thiones with alkyl haloacetates has been studied. It was shown that the reaction proceeds to give S-substituted products. The effect of the nature of the substituents in the molecules of both the thiones and the haloacetates on the reaction route and yields has been examined.

PAGES

488-491

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-012-1020-4

DOI

http://dx.doi.org/10.1007/s10593-012-1020-4

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1043257140


Indexing Status Check whether this publication has been indexed by Scopus and Web Of Science using the SN Indexing Status Tool
Incoming Citations Browse incoming citations for this publication using opencitations.net

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/2008/0305", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Organic Chemistry", 
        "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": "Academy of Sciences Republic of Uzbekistan", 
          "id": "https://www.grid.ac/institutes/grid.419209.7", 
          "name": [
            "S. Yu. Yunusov Institute for the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, 77 Mirzo Ulugbek Ave., 100170, Tashkent, Uzbekistan"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Ziyaev", 
        "givenName": "A. A.", 
        "id": "sg:person.01340367264.28", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01340367264.28"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Academy of Sciences Republic of Uzbekistan", 
          "id": "https://www.grid.ac/institutes/grid.419209.7", 
          "name": [
            "S. Yu. Yunusov Institute for the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, 77 Mirzo Ulugbek Ave., 100170, Tashkent, Uzbekistan"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Tozhiev", 
        "givenName": "I. F.", 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Academy of Sciences Republic of Uzbekistan", 
          "id": "https://www.grid.ac/institutes/grid.419209.7", 
          "name": [
            "S. Yu. Yunusov Institute for the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, 77 Mirzo Ulugbek Ave., 100170, Tashkent, Uzbekistan"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Shakhidoyatov", 
        "givenName": "Kh. M.", 
        "id": "sg:person.015706066705.62", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015706066705.62"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "https://doi.org/10.1002/jhet.5570210141", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1013174332"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570210141", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1013174332"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2012-06", 
    "datePublishedReg": "2012-06-01", 
    "description": "The reaction of 5-aryl-1,3,4-oxadiazoline-2(3H)-thiones with alkyl haloacetates has been studied. It was shown that the reaction proceeds to give S-substituted products. The effect of the nature of the substituents in the molecules of both the thiones and the haloacetates on the reaction route and yields has been examined.", 
    "genre": "research_article", 
    "id": "sg:pub.10.1007/s10593-012-1020-4", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1356886", 
        "issn": [
          "0009-3122", 
          "1573-8353"
        ], 
        "name": "Chemistry of Heterocyclic Compounds", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "3", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "48"
      }
    ], 
    "name": "5-Aryl-1,3,4-oxadiazoline-2(3H)-thiones in reactions with alkyl haloacetates", 
    "pagination": "488-491", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "ce0c5aa0912a9ecb02796183f71568a59064033978f9e96c6f1ce5c34b2a2b31"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s10593-012-1020-4"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1043257140"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s10593-012-1020-4", 
      "https://app.dimensions.ai/details/publication/pub.1043257140"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-10T18:21", 
    "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_8675_00000515.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "http://link.springer.com/10.1007%2Fs10593-012-1020-4"
  }
]
 

Download the RDF metadata as:  json-ld nt turtle xml License info

HOW TO GET THIS DATA PROGRAMMATICALLY:

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.10.1007/s10593-012-1020-4'

N-Triples is a line-based linked data format ideal for batch operations.

curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1007/s10593-012-1020-4'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s10593-012-1020-4'

RDF/XML is a standard XML format for linked data.

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s10593-012-1020-4'


 

This table displays all metadata directly associated to this object as RDF triples.

77 TRIPLES      21 PREDICATES      28 URIs      19 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s10593-012-1020-4 schema:about anzsrc-for:03
2 anzsrc-for:0305
3 schema:author Nc00dd81e2c894915b8f621993fd8317d
4 schema:citation https://doi.org/10.1002/jhet.5570210141
5 schema:datePublished 2012-06
6 schema:datePublishedReg 2012-06-01
7 schema:description The reaction of 5-aryl-1,3,4-oxadiazoline-2(3H)-thiones with alkyl haloacetates has been studied. It was shown that the reaction proceeds to give S-substituted products. The effect of the nature of the substituents in the molecules of both the thiones and the haloacetates on the reaction route and yields has been examined.
8 schema:genre research_article
9 schema:inLanguage en
10 schema:isAccessibleForFree false
11 schema:isPartOf N2694c6d9b67a4f44a7618d6913b080d2
12 N71f1c666632f41d6a0db48c30d57b4df
13 sg:journal.1356886
14 schema:name 5-Aryl-1,3,4-oxadiazoline-2(3H)-thiones in reactions with alkyl haloacetates
15 schema:pagination 488-491
16 schema:productId N16e3fc1208034bae86f127c2b764ac42
17 N53f8447af20e4911aadd402b1703efc2
18 Nfefc60965cfa42ad9031f25e165e0481
19 schema:sameAs https://app.dimensions.ai/details/publication/pub.1043257140
20 https://doi.org/10.1007/s10593-012-1020-4
21 schema:sdDatePublished 2019-04-10T18:21
22 schema:sdLicense https://scigraph.springernature.com/explorer/license/
23 schema:sdPublisher Nd476f66a7cc846a1a16fddf3d197ccf4
24 schema:url http://link.springer.com/10.1007%2Fs10593-012-1020-4
25 sgo:license sg:explorer/license/
26 sgo:sdDataset articles
27 rdf:type schema:ScholarlyArticle
28 N16e3fc1208034bae86f127c2b764ac42 schema:name readcube_id
29 schema:value ce0c5aa0912a9ecb02796183f71568a59064033978f9e96c6f1ce5c34b2a2b31
30 rdf:type schema:PropertyValue
31 N2694c6d9b67a4f44a7618d6913b080d2 schema:issueNumber 3
32 rdf:type schema:PublicationIssue
33 N53f8447af20e4911aadd402b1703efc2 schema:name dimensions_id
34 schema:value pub.1043257140
35 rdf:type schema:PropertyValue
36 N64dccb362a7841b8b1d1c9d0f946fcd7 schema:affiliation https://www.grid.ac/institutes/grid.419209.7
37 schema:familyName Tozhiev
38 schema:givenName I. F.
39 rdf:type schema:Person
40 N71f1c666632f41d6a0db48c30d57b4df schema:volumeNumber 48
41 rdf:type schema:PublicationVolume
42 N9a98964942da4640a99b073f5fe90897 rdf:first sg:person.015706066705.62
43 rdf:rest rdf:nil
44 Nc00dd81e2c894915b8f621993fd8317d rdf:first sg:person.01340367264.28
45 rdf:rest Ndecf38b6ed0b4f238fabb272c1b18a1f
46 Nd476f66a7cc846a1a16fddf3d197ccf4 schema:name Springer Nature - SN SciGraph project
47 rdf:type schema:Organization
48 Ndecf38b6ed0b4f238fabb272c1b18a1f rdf:first N64dccb362a7841b8b1d1c9d0f946fcd7
49 rdf:rest N9a98964942da4640a99b073f5fe90897
50 Nfefc60965cfa42ad9031f25e165e0481 schema:name doi
51 schema:value 10.1007/s10593-012-1020-4
52 rdf:type schema:PropertyValue
53 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
54 schema:name Chemical Sciences
55 rdf:type schema:DefinedTerm
56 anzsrc-for:0305 schema:inDefinedTermSet anzsrc-for:
57 schema:name Organic Chemistry
58 rdf:type schema:DefinedTerm
59 sg:journal.1356886 schema:issn 0009-3122
60 1573-8353
61 schema:name Chemistry of Heterocyclic Compounds
62 rdf:type schema:Periodical
63 sg:person.01340367264.28 schema:affiliation https://www.grid.ac/institutes/grid.419209.7
64 schema:familyName Ziyaev
65 schema:givenName A. A.
66 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01340367264.28
67 rdf:type schema:Person
68 sg:person.015706066705.62 schema:affiliation https://www.grid.ac/institutes/grid.419209.7
69 schema:familyName Shakhidoyatov
70 schema:givenName Kh. M.
71 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015706066705.62
72 rdf:type schema:Person
73 https://doi.org/10.1002/jhet.5570210141 schema:sameAs https://app.dimensions.ai/details/publication/pub.1013174332
74 rdf:type schema:CreativeWork
75 https://www.grid.ac/institutes/grid.419209.7 schema:alternateName Academy of Sciences Republic of Uzbekistan
76 schema:name S. Yu. Yunusov Institute for the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, 77 Mirzo Ulugbek Ave., 100170, Tashkent, Uzbekistan
77 rdf:type schema:Organization
 




Preview window. Press ESC to close (or click here)


...