Chemistry of furazano[3,4-b]pyrazine. 4. 5,6-Dichlorofurazano[3,4-b]pyrazine in cyclization reactions View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1997-11

AUTHORS

I. B. Starchenkov, V. G. Andrianov

ABSTRACT

A method was developed for the production of polycyclic compounds containing the furazano[3,4-b]pyrazine fragment by the reaction of difunctional nucleophiles with 5,6-dichlorofurazano[3,4-b]pyrazine. It was shown that the reaction is affected by the hydrogen chloride acceptor (triethylamine).

PAGES

1352-1354

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf02320341

DOI

http://dx.doi.org/10.1007/bf02320341

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1053085520


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"
      }, 
      {
        "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": [
      {
        "familyName": "Starchenkov", 
        "givenName": "I. B.", 
        "id": "sg:person.014640002305.16", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014640002305.16"
        ], 
        "type": "Person"
      }, 
      {
        "familyName": "Andrianov", 
        "givenName": "V. G.", 
        "id": "sg:person.016164060371.30", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016164060371.30"
        ], 
        "type": "Person"
      }
    ], 
    "datePublished": "1997-11", 
    "datePublishedReg": "1997-11-01", 
    "description": "A method was developed for the production of polycyclic compounds containing the furazano[3,4-b]pyrazine fragment by the reaction of difunctional nucleophiles with 5,6-dichlorofurazano[3,4-b]pyrazine. It was shown that the reaction is affected by the hydrogen chloride acceptor (triethylamine).", 
    "genre": "article", 
    "id": "sg:pub.10.1007/bf02320341", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1429545", 
        "issn": [
          "0132-6244", 
          "1573-8353"
        ], 
        "name": "Chemistry of Heterocyclic Compounds", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "11", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "33"
      }
    ], 
    "keywords": [
      "hydrogen chloride acceptor", 
      "chloride acceptor", 
      "polycyclic compounds", 
      "difunctional nucleophiles", 
      "cyclization reaction", 
      "reaction", 
      "chemistry", 
      "nucleophiles", 
      "acceptor", 
      "compounds", 
      "fragments", 
      "method", 
      "production"
    ], 
    "name": "Chemistry of furazano[3,4-b]pyrazine. 4. 5,6-Dichlorofurazano[3,4-b]pyrazine in cyclization reactions", 
    "pagination": "1352-1354", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1053085520"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/bf02320341"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/bf02320341", 
      "https://app.dimensions.ai/details/publication/pub.1053085520"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-12-01T06:21", 
    "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_259.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/bf02320341"
  }
]
 

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/bf02320341'

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/bf02320341'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf02320341'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf02320341'


 

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

76 TRIPLES      20 PREDICATES      39 URIs      30 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/bf02320341 schema:about anzsrc-for:03
2 anzsrc-for:0305
3 anzsrc-for:0306
4 schema:author Nb44719d96bc84822a022fa4b03f385e0
5 schema:datePublished 1997-11
6 schema:datePublishedReg 1997-11-01
7 schema:description A method was developed for the production of polycyclic compounds containing the furazano[3,4-b]pyrazine fragment by the reaction of difunctional nucleophiles with 5,6-dichlorofurazano[3,4-b]pyrazine. It was shown that the reaction is affected by the hydrogen chloride acceptor (triethylamine).
8 schema:genre article
9 schema:isAccessibleForFree false
10 schema:isPartOf N10933d73fe8544d28c3fd6c5f3294c04
11 Naa5b6d828e564ebfbd04db087aff76f7
12 sg:journal.1429545
13 schema:keywords acceptor
14 chemistry
15 chloride acceptor
16 compounds
17 cyclization reaction
18 difunctional nucleophiles
19 fragments
20 hydrogen chloride acceptor
21 method
22 nucleophiles
23 polycyclic compounds
24 production
25 reaction
26 schema:name Chemistry of furazano[3,4-b]pyrazine. 4. 5,6-Dichlorofurazano[3,4-b]pyrazine in cyclization reactions
27 schema:pagination 1352-1354
28 schema:productId N33a8f73d32c14d899902871ad6c5d345
29 Na4a543228a67476abeffb299bd6dbde9
30 schema:sameAs https://app.dimensions.ai/details/publication/pub.1053085520
31 https://doi.org/10.1007/bf02320341
32 schema:sdDatePublished 2022-12-01T06:21
33 schema:sdLicense https://scigraph.springernature.com/explorer/license/
34 schema:sdPublisher Nbe56456f2da0421aa4748f9107c87f13
35 schema:url https://doi.org/10.1007/bf02320341
36 sgo:license sg:explorer/license/
37 sgo:sdDataset articles
38 rdf:type schema:ScholarlyArticle
39 N10933d73fe8544d28c3fd6c5f3294c04 schema:issueNumber 11
40 rdf:type schema:PublicationIssue
41 N2ab28c90d72b4fdcad95b22c5e7100ba rdf:first sg:person.016164060371.30
42 rdf:rest rdf:nil
43 N33a8f73d32c14d899902871ad6c5d345 schema:name dimensions_id
44 schema:value pub.1053085520
45 rdf:type schema:PropertyValue
46 Na4a543228a67476abeffb299bd6dbde9 schema:name doi
47 schema:value 10.1007/bf02320341
48 rdf:type schema:PropertyValue
49 Naa5b6d828e564ebfbd04db087aff76f7 schema:volumeNumber 33
50 rdf:type schema:PublicationVolume
51 Nb44719d96bc84822a022fa4b03f385e0 rdf:first sg:person.014640002305.16
52 rdf:rest N2ab28c90d72b4fdcad95b22c5e7100ba
53 Nbe56456f2da0421aa4748f9107c87f13 schema:name Springer Nature - SN SciGraph project
54 rdf:type schema:Organization
55 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
56 schema:name Chemical Sciences
57 rdf:type schema:DefinedTerm
58 anzsrc-for:0305 schema:inDefinedTermSet anzsrc-for:
59 schema:name Organic Chemistry
60 rdf:type schema:DefinedTerm
61 anzsrc-for:0306 schema:inDefinedTermSet anzsrc-for:
62 schema:name Physical Chemistry (incl. Structural)
63 rdf:type schema:DefinedTerm
64 sg:journal.1429545 schema:issn 0132-6244
65 1573-8353
66 schema:name Chemistry of Heterocyclic Compounds
67 schema:publisher Springer Nature
68 rdf:type schema:Periodical
69 sg:person.014640002305.16 schema:familyName Starchenkov
70 schema:givenName I. B.
71 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014640002305.16
72 rdf:type schema:Person
73 sg:person.016164060371.30 schema:familyName Andrianov
74 schema:givenName V. G.
75 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016164060371.30
76 rdf:type schema:Person
 




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


...