Synthesis of fluorine-containing analogs of ellipticine and other heterocycles from 2-Nitro-and 2-amino-4,5-difluoroanilines View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2007-09

AUTHORS

V. N. Yarovenko, A. V. Polushina, K. S. Levchenko, I. V. Zavarzin, M. M. Krayushkin, S. K. Kotovskaya, V. N. Charushin

ABSTRACT

2-Nitro- and 2-amino-4,5-difluoroanilines were used as starting materials to synthesize fluorine-containing imidazole, oxazole, and indoloquinoxaline derivatives. The latter may be regarded as ellipticine analogs.

PAGES

1387-1392

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070428007090217

DOI

http://dx.doi.org/10.1134/s1070428007090217

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1031359394


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": "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia", 
          "id": "http://www.grid.ac/institutes/grid.4886.2", 
          "name": [
            "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Yarovenko", 
        "givenName": "V. N.", 
        "id": "sg:person.013442641550.93", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013442641550.93"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia", 
          "id": "http://www.grid.ac/institutes/grid.4886.2", 
          "name": [
            "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Polushina", 
        "givenName": "A. V.", 
        "id": "sg:person.013137106004.40", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013137106004.40"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia", 
          "id": "http://www.grid.ac/institutes/grid.4886.2", 
          "name": [
            "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Levchenko", 
        "givenName": "K. S.", 
        "id": "sg:person.014302146365.38", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014302146365.38"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia", 
          "id": "http://www.grid.ac/institutes/grid.4886.2", 
          "name": [
            "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Zavarzin", 
        "givenName": "I. V.", 
        "id": "sg:person.011151201037.74", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011151201037.74"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia", 
          "id": "http://www.grid.ac/institutes/grid.4886.2", 
          "name": [
            "Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Krayushkin", 
        "givenName": "M. M.", 
        "id": "sg:person.015607156041.14", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015607156041.14"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Ural State Technical University, Yekaterinburg, Russia", 
          "id": "http://www.grid.ac/institutes/grid.412761.7", 
          "name": [
            "Ural State Technical University, Yekaterinburg, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Kotovskaya", 
        "givenName": "S. K.", 
        "id": "sg:person.0713503500.63", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0713503500.63"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Postovskii Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, ul. S. Kovalevskoi 20, 620219, Yekaterinburg, Russia", 
          "id": "http://www.grid.ac/institutes/grid.426536.0", 
          "name": [
            "Postovskii Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, ul. S. Kovalevskoi 20, 620219, Yekaterinburg, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Charushin", 
        "givenName": "V. N.", 
        "id": "sg:person.011223315622.12", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011223315622.12"
        ], 
        "type": "Person"
      }
    ], 
    "datePublished": "2007-09", 
    "datePublishedReg": "2007-09-01", 
    "description": "Abstract2-Nitro- and 2-amino-4,5-difluoroanilines were used as starting materials to synthesize fluorine-containing imidazole, oxazole, and indoloquinoxaline derivatives. The latter may be regarded as ellipticine analogs.", 
    "genre": "article", 
    "id": "sg:pub.10.1134/s1070428007090217", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1136317", 
        "issn": [
          "1070-4280", 
          "1608-3393"
        ], 
        "name": "Russian Journal of Organic Chemistry", 
        "publisher": "Pleiades Publishing", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "9", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "43"
      }
    ], 
    "keywords": [
      "fluorine-containing analogues", 
      "indoloquinoxaline derivatives", 
      "ellipticine analogues", 
      "difluoroaniline", 
      "heterocycles", 
      "oxazoles", 
      "imidazole", 
      "analogues", 
      "synthesis", 
      "derivatives", 
      "materials", 
      "latter"
    ], 
    "name": "Synthesis of fluorine-containing analogs of ellipticine and other heterocycles from 2-Nitro-and 2-amino-4,5-difluoroanilines", 
    "pagination": "1387-1392", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1031359394"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1134/s1070428007090217"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1134/s1070428007090217", 
      "https://app.dimensions.ai/details/publication/pub.1031359394"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-12-01T06:26", 
    "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_444.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1134/s1070428007090217"
  }
]
 

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/s1070428007090217'

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/s1070428007090217'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1134/s1070428007090217'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1134/s1070428007090217'


 

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

117 TRIPLES      20 PREDICATES      37 URIs      29 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1134/s1070428007090217 schema:about anzsrc-for:03
2 anzsrc-for:0305
3 schema:author Nefada115011c4c7ba206dc0f059fec61
4 schema:datePublished 2007-09
5 schema:datePublishedReg 2007-09-01
6 schema:description Abstract2-Nitro- and 2-amino-4,5-difluoroanilines were used as starting materials to synthesize fluorine-containing imidazole, oxazole, and indoloquinoxaline derivatives. The latter may be regarded as ellipticine analogs.
7 schema:genre article
8 schema:isAccessibleForFree false
9 schema:isPartOf N5f49b9fa82584ae689db19117e2add70
10 Nb0f85f692bc94435ac7a77b5972d3c14
11 sg:journal.1136317
12 schema:keywords analogues
13 derivatives
14 difluoroaniline
15 ellipticine analogues
16 fluorine-containing analogues
17 heterocycles
18 imidazole
19 indoloquinoxaline derivatives
20 latter
21 materials
22 oxazoles
23 synthesis
24 schema:name Synthesis of fluorine-containing analogs of ellipticine and other heterocycles from 2-Nitro-and 2-amino-4,5-difluoroanilines
25 schema:pagination 1387-1392
26 schema:productId N97d4e3d0c4fa48b8a9fbab8a8a98c2b1
27 Na637cd1dcf864bc1972d1f4e68309266
28 schema:sameAs https://app.dimensions.ai/details/publication/pub.1031359394
29 https://doi.org/10.1134/s1070428007090217
30 schema:sdDatePublished 2022-12-01T06:26
31 schema:sdLicense https://scigraph.springernature.com/explorer/license/
32 schema:sdPublisher N37b1822ced4943bf9beead2db0aa4684
33 schema:url https://doi.org/10.1134/s1070428007090217
34 sgo:license sg:explorer/license/
35 sgo:sdDataset articles
36 rdf:type schema:ScholarlyArticle
37 N049bd5d30a66453a82f600e6375d687e rdf:first sg:person.015607156041.14
38 rdf:rest N10d7f39f07974b7abe2ab48e70efed92
39 N10d7f39f07974b7abe2ab48e70efed92 rdf:first sg:person.0713503500.63
40 rdf:rest N214dcaf9b4c847ec95f3b1bb0c3aa979
41 N214dcaf9b4c847ec95f3b1bb0c3aa979 rdf:first sg:person.011223315622.12
42 rdf:rest rdf:nil
43 N2964438105be4cdea14ec65f3565bee1 rdf:first sg:person.014302146365.38
44 rdf:rest N59a9ced554cf4cfead539dfe78b6248f
45 N37b1822ced4943bf9beead2db0aa4684 schema:name Springer Nature - SN SciGraph project
46 rdf:type schema:Organization
47 N59a9ced554cf4cfead539dfe78b6248f rdf:first sg:person.011151201037.74
48 rdf:rest N049bd5d30a66453a82f600e6375d687e
49 N5f49b9fa82584ae689db19117e2add70 schema:volumeNumber 43
50 rdf:type schema:PublicationVolume
51 N97d4e3d0c4fa48b8a9fbab8a8a98c2b1 schema:name dimensions_id
52 schema:value pub.1031359394
53 rdf:type schema:PropertyValue
54 Na637cd1dcf864bc1972d1f4e68309266 schema:name doi
55 schema:value 10.1134/s1070428007090217
56 rdf:type schema:PropertyValue
57 Nb0f85f692bc94435ac7a77b5972d3c14 schema:issueNumber 9
58 rdf:type schema:PublicationIssue
59 Nefada115011c4c7ba206dc0f059fec61 rdf:first sg:person.013442641550.93
60 rdf:rest Nf1161affcfe54758aaee743274481750
61 Nf1161affcfe54758aaee743274481750 rdf:first sg:person.013137106004.40
62 rdf:rest N2964438105be4cdea14ec65f3565bee1
63 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
64 schema:name Chemical Sciences
65 rdf:type schema:DefinedTerm
66 anzsrc-for:0305 schema:inDefinedTermSet anzsrc-for:
67 schema:name Organic Chemistry
68 rdf:type schema:DefinedTerm
69 sg:journal.1136317 schema:issn 1070-4280
70 1608-3393
71 schema:name Russian Journal of Organic Chemistry
72 schema:publisher Pleiades Publishing
73 rdf:type schema:Periodical
74 sg:person.011151201037.74 schema:affiliation grid-institutes:grid.4886.2
75 schema:familyName Zavarzin
76 schema:givenName I. V.
77 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011151201037.74
78 rdf:type schema:Person
79 sg:person.011223315622.12 schema:affiliation grid-institutes:grid.426536.0
80 schema:familyName Charushin
81 schema:givenName V. N.
82 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011223315622.12
83 rdf:type schema:Person
84 sg:person.013137106004.40 schema:affiliation grid-institutes:grid.4886.2
85 schema:familyName Polushina
86 schema:givenName A. V.
87 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013137106004.40
88 rdf:type schema:Person
89 sg:person.013442641550.93 schema:affiliation grid-institutes:grid.4886.2
90 schema:familyName Yarovenko
91 schema:givenName V. N.
92 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013442641550.93
93 rdf:type schema:Person
94 sg:person.014302146365.38 schema:affiliation grid-institutes:grid.4886.2
95 schema:familyName Levchenko
96 schema:givenName K. S.
97 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014302146365.38
98 rdf:type schema:Person
99 sg:person.015607156041.14 schema:affiliation grid-institutes:grid.4886.2
100 schema:familyName Krayushkin
101 schema:givenName M. M.
102 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015607156041.14
103 rdf:type schema:Person
104 sg:person.0713503500.63 schema:affiliation grid-institutes:grid.412761.7
105 schema:familyName Kotovskaya
106 schema:givenName S. K.
107 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0713503500.63
108 rdf:type schema:Person
109 grid-institutes:grid.412761.7 schema:alternateName Ural State Technical University, Yekaterinburg, Russia
110 schema:name Ural State Technical University, Yekaterinburg, Russia
111 rdf:type schema:Organization
112 grid-institutes:grid.426536.0 schema:alternateName Postovskii Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, ul. S. Kovalevskoi 20, 620219, Yekaterinburg, Russia
113 schema:name Postovskii Institute of Organic Synthesis, Ural Division, Russian Academy of Sciences, ul. S. Kovalevskoi 20, 620219, Yekaterinburg, Russia
114 rdf:type schema:Organization
115 grid-institutes:grid.4886.2 schema:alternateName Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia
116 schema:name Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Leninskii pr. 47, 119991, Moscow, Russia
117 rdf:type schema:Organization
 




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


...