Synthesis of new quinoxaline derivatives View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2012-02

AUTHORS

O. B. Laskina, S. F. Mel’nikova, I. V. Tselinskii

ABSTRACT

Proceeding from 2-aminoquinoxaline-3-carbonitrile 1,4-dioxides new derivatives of quinoxaline and quinoxaline 1,4-dioxide were synthesized containing in the position 3 of the quinoxaline fragment 1,2,4-oxadiazole and tetrazole rings. The acylation of 2-amino-N′-hydroxyquinoxaline-3-carbox imidoamide 1,4-dioxide was investigated.

PAGES

278-283

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070428012020194

DOI

http://dx.doi.org/10.1134/s1070428012020194

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1047973259


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/2008/03", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Chemical Sciences", 
        "type": "DefinedTerm"
      }, 
      {
        "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"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "St. Petersburg State Technological Institute (Technical University), 190013, St. Petersburg, Russia", 
          "id": "http://www.grid.ac/institutes/grid.437869.7", 
          "name": [
            "St. Petersburg State Technological Institute (Technical University), 190013, St. Petersburg, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Laskina", 
        "givenName": "O. B.", 
        "id": "sg:person.014247101401.29", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014247101401.29"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "St. Petersburg State Technological Institute (Technical University), 190013, St. Petersburg, Russia", 
          "id": "http://www.grid.ac/institutes/grid.437869.7", 
          "name": [
            "St. Petersburg State Technological Institute (Technical University), 190013, St. Petersburg, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Mel\u2019nikova", 
        "givenName": "S. F.", 
        "id": "sg:person.07717041115.30", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07717041115.30"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "St. Petersburg State Technological Institute (Technical University), 190013, St. Petersburg, Russia", 
          "id": "http://www.grid.ac/institutes/grid.437869.7", 
          "name": [
            "St. Petersburg State Technological Institute (Technical University), 190013, St. Petersburg, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Tselinskii", 
        "givenName": "I. V.", 
        "id": "sg:person.015404525675.24", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015404525675.24"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "sg:pub.10.1007/7081_2007_066", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1000920991", 
          "https://doi.org/10.1007/7081_2007_066"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/978-3-662-04201-4", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1013278232", 
          "https://doi.org/10.1007/978-3-662-04201-4"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2012-02", 
    "datePublishedReg": "2012-02-01", 
    "description": "Proceeding from 2-aminoquinoxaline-3-carbonitrile 1,4-dioxides new derivatives of quinoxaline and quinoxaline 1,4-dioxide were synthesized containing in the position 3 of the quinoxaline fragment 1,2,4-oxadiazole and tetrazole rings. The acylation of 2-amino-N\u2032-hydroxyquinoxaline-3-carbox imidoamide 1,4-dioxide was investigated.", 
    "genre": "article", 
    "id": "sg:pub.10.1134/s1070428012020194", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1136317", 
        "issn": [
          "1070-4280", 
          "1608-3393"
        ], 
        "name": "Russian Journal of Organic Chemistry", 
        "publisher": "Pleiades Publishing", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "2", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "48"
      }
    ], 
    "keywords": [
      "new quinoxaline derivatives", 
      "tetrazole ring", 
      "quinoxaline derivatives", 
      "quinoxaline fragments", 
      "new derivatives", 
      "quinoxaline", 
      "position 3", 
      "derivatives", 
      "dioxide", 
      "oxadiazole", 
      "carbox", 
      "synthesis", 
      "acylation", 
      "ring", 
      "fragments"
    ], 
    "name": "Synthesis of new quinoxaline derivatives", 
    "pagination": "278-283", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1047973259"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1134/s1070428012020194"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1134/s1070428012020194", 
      "https://app.dimensions.ai/details/publication/pub.1047973259"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-12-01T06:29", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20221201/entities/gbq_results/article/article_556.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1134/s1070428012020194"
  }
]
 

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.10.1134/s1070428012020194'

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/s1070428012020194'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1134/s1070428012020194'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1134/s1070428012020194'


 

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

94 TRIPLES      21 PREDICATES      42 URIs      32 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1134/s1070428012020194 schema:about anzsrc-for:03
2 anzsrc-for:0305
3 schema:author Nd79e2d3a83764c27ba2740d657f55750
4 schema:citation sg:pub.10.1007/7081_2007_066
5 sg:pub.10.1007/978-3-662-04201-4
6 schema:datePublished 2012-02
7 schema:datePublishedReg 2012-02-01
8 schema:description Proceeding from 2-aminoquinoxaline-3-carbonitrile 1,4-dioxides new derivatives of quinoxaline and quinoxaline 1,4-dioxide were synthesized containing in the position 3 of the quinoxaline fragment 1,2,4-oxadiazole and tetrazole rings. The acylation of 2-amino-N′-hydroxyquinoxaline-3-carbox imidoamide 1,4-dioxide was investigated.
9 schema:genre article
10 schema:isAccessibleForFree false
11 schema:isPartOf N617f7ec8251a4a2a8c6253211765fbb8
12 N65c55f139b2148d2a232f5c6e5f27cef
13 sg:journal.1136317
14 schema:keywords acylation
15 carbox
16 derivatives
17 dioxide
18 fragments
19 new derivatives
20 new quinoxaline derivatives
21 oxadiazole
22 position 3
23 quinoxaline
24 quinoxaline derivatives
25 quinoxaline fragments
26 ring
27 synthesis
28 tetrazole ring
29 schema:name Synthesis of new quinoxaline derivatives
30 schema:pagination 278-283
31 schema:productId N4ec4a8966f864ec4b718614aa70406aa
32 Na1894ed2b0ba46c0bcfa6fc1fd300bdf
33 schema:sameAs https://app.dimensions.ai/details/publication/pub.1047973259
34 https://doi.org/10.1134/s1070428012020194
35 schema:sdDatePublished 2022-12-01T06:29
36 schema:sdLicense https://scigraph.springernature.com/explorer/license/
37 schema:sdPublisher N64ee559d277345b587a21812b76247b7
38 schema:url https://doi.org/10.1134/s1070428012020194
39 sgo:license sg:explorer/license/
40 sgo:sdDataset articles
41 rdf:type schema:ScholarlyArticle
42 N4ec4a8966f864ec4b718614aa70406aa schema:name doi
43 schema:value 10.1134/s1070428012020194
44 rdf:type schema:PropertyValue
45 N617f7ec8251a4a2a8c6253211765fbb8 schema:volumeNumber 48
46 rdf:type schema:PublicationVolume
47 N64ee559d277345b587a21812b76247b7 schema:name Springer Nature - SN SciGraph project
48 rdf:type schema:Organization
49 N65c55f139b2148d2a232f5c6e5f27cef schema:issueNumber 2
50 rdf:type schema:PublicationIssue
51 N7cbcfe6afecb4067bb136178d412df12 rdf:first sg:person.07717041115.30
52 rdf:rest Nfba76c0b9fcf4947a5c93ac93cfa5363
53 Na1894ed2b0ba46c0bcfa6fc1fd300bdf schema:name dimensions_id
54 schema:value pub.1047973259
55 rdf:type schema:PropertyValue
56 Nd79e2d3a83764c27ba2740d657f55750 rdf:first sg:person.014247101401.29
57 rdf:rest N7cbcfe6afecb4067bb136178d412df12
58 Nfba76c0b9fcf4947a5c93ac93cfa5363 rdf:first sg:person.015404525675.24
59 rdf:rest rdf:nil
60 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
61 schema:name Chemical Sciences
62 rdf:type schema:DefinedTerm
63 anzsrc-for:0305 schema:inDefinedTermSet anzsrc-for:
64 schema:name Organic Chemistry
65 rdf:type schema:DefinedTerm
66 sg:journal.1136317 schema:issn 1070-4280
67 1608-3393
68 schema:name Russian Journal of Organic Chemistry
69 schema:publisher Pleiades Publishing
70 rdf:type schema:Periodical
71 sg:person.014247101401.29 schema:affiliation grid-institutes:grid.437869.7
72 schema:familyName Laskina
73 schema:givenName O. B.
74 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014247101401.29
75 rdf:type schema:Person
76 sg:person.015404525675.24 schema:affiliation grid-institutes:grid.437869.7
77 schema:familyName Tselinskii
78 schema:givenName I. V.
79 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015404525675.24
80 rdf:type schema:Person
81 sg:person.07717041115.30 schema:affiliation grid-institutes:grid.437869.7
82 schema:familyName Mel’nikova
83 schema:givenName S. F.
84 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07717041115.30
85 rdf:type schema:Person
86 sg:pub.10.1007/7081_2007_066 schema:sameAs https://app.dimensions.ai/details/publication/pub.1000920991
87 https://doi.org/10.1007/7081_2007_066
88 rdf:type schema:CreativeWork
89 sg:pub.10.1007/978-3-662-04201-4 schema:sameAs https://app.dimensions.ai/details/publication/pub.1013278232
90 https://doi.org/10.1007/978-3-662-04201-4
91 rdf:type schema:CreativeWork
92 grid-institutes:grid.437869.7 schema:alternateName St. Petersburg State Technological Institute (Technical University), 190013, St. Petersburg, Russia
93 schema:name St. Petersburg State Technological Institute (Technical University), 190013, St. Petersburg, Russia
94 rdf:type schema:Organization
 




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


...