Heterocycles with a β-nitroenamine fragment View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1999-06

AUTHORS

V. P. Kislyi, V. N. Nesterov, V. V. Semenov

ABSTRACT

The reaction of 3-cyanopyridine-2(1H)-thiones with bromonitromethane in the presence of triethylamine results in 3-amino-2-nitrothieno[2,3-b]pyridines. The crystal and molecular structure of one of the reaction products was established by X-ray diffraction analysis.

PAGES

1139-1142

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf02496017

DOI

http://dx.doi.org/10.1007/bf02496017

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1007890871


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/2008/0303", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Macromolecular and Materials Chemistry", 
        "type": "DefinedTerm"
      }, 
      {
        "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"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 117913, Moscow, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.439283.7", 
          "name": [
            "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 117913, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Kislyi", 
        "givenName": "V. P.", 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813, Moscow, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.431939.5", 
          "name": [
            "A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Nesterov", 
        "givenName": "V. N.", 
        "id": "sg:person.0777374631.34", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0777374631.34"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 117913, Moscow, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.439283.7", 
          "name": [
            "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 117913, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Semenov", 
        "givenName": "V. V.", 
        "id": "sg:person.0716636167.19", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0716636167.19"
        ], 
        "type": "Person"
      }
    ], 
    "datePublished": "1999-06", 
    "datePublishedReg": "1999-06-01", 
    "description": "The reaction of 3-cyanopyridine-2(1H)-thiones with bromonitromethane in the presence of triethylamine results in 3-amino-2-nitrothieno[2,3-b]pyridines. The crystal and molecular structure of one of the reaction products was established by X-ray diffraction analysis.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/bf02496017", 
    "inLanguage": "en", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1022309", 
        "issn": [
          "1063-5211", 
          "1026-3500"
        ], 
        "name": "Russian Chemical Bulletin", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "6", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "48"
      }
    ], 
    "keywords": [
      "ray diffraction analysis", 
      "triethylamine results", 
      "molecular structure", 
      "diffraction analysis", 
      "reaction products", 
      "heterocycles", 
      "bromonitromethane", 
      "reaction", 
      "crystals", 
      "products", 
      "structure", 
      "presence", 
      "fragments", 
      "analysis", 
      "results", 
      "nitroenamine fragment"
    ], 
    "name": "Heterocycles with a \u03b2-nitroenamine fragment", 
    "pagination": "1139-1142", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1007890871"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/bf02496017"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/bf02496017", 
      "https://app.dimensions.ai/details/publication/pub.1007890871"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2021-11-01T18:04", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20211101/entities/gbq_results/article/article_319.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/bf02496017"
  }
]
 

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/bf02496017'

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/bf02496017'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf02496017'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf02496017'


 

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

94 TRIPLES      21 PREDICATES      43 URIs      34 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/bf02496017 schema:about anzsrc-for:03
2 anzsrc-for:0303
3 anzsrc-for:0306
4 schema:author N754ac93d9132416880ef6fb637d504c3
5 schema:datePublished 1999-06
6 schema:datePublishedReg 1999-06-01
7 schema:description The reaction of 3-cyanopyridine-2(1H)-thiones with bromonitromethane in the presence of triethylamine results in 3-amino-2-nitrothieno[2,3-b]pyridines. The crystal and molecular structure of one of the reaction products was established by X-ray diffraction analysis.
8 schema:genre article
9 schema:inLanguage en
10 schema:isAccessibleForFree false
11 schema:isPartOf Nd8b60ef810544a4da651790415058e80
12 Nf471234b956f4e47a7f710a074dc6dc1
13 sg:journal.1022309
14 schema:keywords analysis
15 bromonitromethane
16 crystals
17 diffraction analysis
18 fragments
19 heterocycles
20 molecular structure
21 nitroenamine fragment
22 presence
23 products
24 ray diffraction analysis
25 reaction
26 reaction products
27 results
28 structure
29 triethylamine results
30 schema:name Heterocycles with a β-nitroenamine fragment
31 schema:pagination 1139-1142
32 schema:productId N84659011b3d14a01962cebd8af62e48a
33 Nd5c453fc76fa4125b8210cdcd2c7683c
34 schema:sameAs https://app.dimensions.ai/details/publication/pub.1007890871
35 https://doi.org/10.1007/bf02496017
36 schema:sdDatePublished 2021-11-01T18:04
37 schema:sdLicense https://scigraph.springernature.com/explorer/license/
38 schema:sdPublisher Nf1249f0e1ee1443ca721443da82b0524
39 schema:url https://doi.org/10.1007/bf02496017
40 sgo:license sg:explorer/license/
41 sgo:sdDataset articles
42 rdf:type schema:ScholarlyArticle
43 N61d43d3995be4e15beca533eb4e39dfb schema:affiliation grid-institutes:grid.439283.7
44 schema:familyName Kislyi
45 schema:givenName V. P.
46 rdf:type schema:Person
47 N6513971c73fa4589b77f29614ba30b18 rdf:first sg:person.0716636167.19
48 rdf:rest rdf:nil
49 N754ac93d9132416880ef6fb637d504c3 rdf:first N61d43d3995be4e15beca533eb4e39dfb
50 rdf:rest Ne9322bbf4fd644d2ab9783572ee203ed
51 N84659011b3d14a01962cebd8af62e48a schema:name doi
52 schema:value 10.1007/bf02496017
53 rdf:type schema:PropertyValue
54 Nd5c453fc76fa4125b8210cdcd2c7683c schema:name dimensions_id
55 schema:value pub.1007890871
56 rdf:type schema:PropertyValue
57 Nd8b60ef810544a4da651790415058e80 schema:volumeNumber 48
58 rdf:type schema:PublicationVolume
59 Ne9322bbf4fd644d2ab9783572ee203ed rdf:first sg:person.0777374631.34
60 rdf:rest N6513971c73fa4589b77f29614ba30b18
61 Nf1249f0e1ee1443ca721443da82b0524 schema:name Springer Nature - SN SciGraph project
62 rdf:type schema:Organization
63 Nf471234b956f4e47a7f710a074dc6dc1 schema:issueNumber 6
64 rdf:type schema:PublicationIssue
65 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
66 schema:name Chemical Sciences
67 rdf:type schema:DefinedTerm
68 anzsrc-for:0303 schema:inDefinedTermSet anzsrc-for:
69 schema:name Macromolecular and Materials Chemistry
70 rdf:type schema:DefinedTerm
71 anzsrc-for:0306 schema:inDefinedTermSet anzsrc-for:
72 schema:name Physical Chemistry (incl. Structural)
73 rdf:type schema:DefinedTerm
74 sg:journal.1022309 schema:issn 1026-3500
75 1063-5211
76 schema:name Russian Chemical Bulletin
77 schema:publisher Springer Nature
78 rdf:type schema:Periodical
79 sg:person.0716636167.19 schema:affiliation grid-institutes:grid.439283.7
80 schema:familyName Semenov
81 schema:givenName V. V.
82 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0716636167.19
83 rdf:type schema:Person
84 sg:person.0777374631.34 schema:affiliation grid-institutes:grid.431939.5
85 schema:familyName Nesterov
86 schema:givenName V. N.
87 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0777374631.34
88 rdf:type schema:Person
89 grid-institutes:grid.431939.5 schema:alternateName A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813, Moscow, Russian Federation
90 schema:name A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813, Moscow, Russian Federation
91 rdf:type schema:Organization
92 grid-institutes:grid.439283.7 schema:alternateName N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 117913, Moscow, Russian Federation
93 schema:name N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 117913, Moscow, Russian Federation
94 rdf:type schema:Organization
 




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


...