Reaction of imidazole and its 2-alkyl derivatives with γ-butyrolactone View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1992-11

AUTHORS

O. K. Shevchenko, A. T. Ayupova, G. G. Galust'yan

ABSTRACT

Reaction of imidazole with γ-butyrolactone gives N-alkylation and N-acylation products depending upon the reaction conditions.

PAGES

1274-1276

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00532076

DOI

http://dx.doi.org/10.1007/bf00532076

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1008294832


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": "Institute for the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, 700170, Tashkent", 
          "id": "http://www.grid.ac/institutes/grid.419209.7", 
          "name": [
            "Institute for the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, 700170, Tashkent"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Shevchenko", 
        "givenName": "O. K.", 
        "id": "sg:person.012433102130.12", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012433102130.12"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute for the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, 700170, Tashkent", 
          "id": "http://www.grid.ac/institutes/grid.419209.7", 
          "name": [
            "Institute for the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, 700170, Tashkent"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Ayupova", 
        "givenName": "A. T.", 
        "id": "sg:person.010476772135.01", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010476772135.01"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute for the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, 700170, Tashkent", 
          "id": "http://www.grid.ac/institutes/grid.419209.7", 
          "name": [
            "Institute for the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, 700170, Tashkent"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Galust'yan", 
        "givenName": "G. G.", 
        "id": "sg:person.010647660001.34", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010647660001.34"
        ], 
        "type": "Person"
      }
    ], 
    "datePublished": "1992-11", 
    "datePublishedReg": "1992-11-01", 
    "description": "Reaction of imidazole with \u03b3-butyrolactone gives N-alkylation and N-acylation products depending upon the reaction conditions.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/bf00532076", 
    "inLanguage": "en", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1358699", 
        "issn": [
          "0132-6244", 
          "1573-8353"
        ], 
        "name": "Chemistry of Heterocyclic Compounds", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "11", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "28"
      }
    ], 
    "keywords": [
      "reaction", 
      "conditions", 
      "reaction of imidazole", 
      "derivatives", 
      "imidazole", 
      "products", 
      "reaction conditions", 
      "acylation products", 
      "butyrolactone", 
      "alkylation"
    ], 
    "name": "Reaction of imidazole and its 2-alkyl derivatives with \u03b3-butyrolactone", 
    "pagination": "1274-1276", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1008294832"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/bf00532076"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/bf00532076", 
      "https://app.dimensions.ai/details/publication/pub.1008294832"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2021-12-01T19:07", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20211201/entities/gbq_results/article/article_221.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/bf00532076"
  }
]
 

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/bf00532076'

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/bf00532076'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf00532076'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf00532076'


 

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

82 TRIPLES      21 PREDICATES      36 URIs      28 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/bf00532076 schema:about anzsrc-for:03
2 anzsrc-for:0305
3 schema:author N12480890a23641f6a3037e4612f83937
4 schema:datePublished 1992-11
5 schema:datePublishedReg 1992-11-01
6 schema:description Reaction of imidazole with γ-butyrolactone gives N-alkylation and N-acylation products depending upon the reaction conditions.
7 schema:genre article
8 schema:inLanguage en
9 schema:isAccessibleForFree false
10 schema:isPartOf N03e934b6ee6246cf8596777674d6ff2d
11 N6790fb73be29411f966fb182cbedf1d6
12 sg:journal.1358699
13 schema:keywords acylation products
14 alkylation
15 butyrolactone
16 conditions
17 derivatives
18 imidazole
19 products
20 reaction
21 reaction conditions
22 reaction of imidazole
23 schema:name Reaction of imidazole and its 2-alkyl derivatives with γ-butyrolactone
24 schema:pagination 1274-1276
25 schema:productId N6af1645b03454a0fa4a773a75638198a
26 Na7a5e9830ce54fe395cf2fc5e2085ff3
27 schema:sameAs https://app.dimensions.ai/details/publication/pub.1008294832
28 https://doi.org/10.1007/bf00532076
29 schema:sdDatePublished 2021-12-01T19:07
30 schema:sdLicense https://scigraph.springernature.com/explorer/license/
31 schema:sdPublisher N2987b27ac7c64122a18e271b4102fc1a
32 schema:url https://doi.org/10.1007/bf00532076
33 sgo:license sg:explorer/license/
34 sgo:sdDataset articles
35 rdf:type schema:ScholarlyArticle
36 N03e934b6ee6246cf8596777674d6ff2d schema:volumeNumber 28
37 rdf:type schema:PublicationVolume
38 N12480890a23641f6a3037e4612f83937 rdf:first sg:person.012433102130.12
39 rdf:rest Nf88373aec8b440d68b5b5d8d1d0bac52
40 N2987b27ac7c64122a18e271b4102fc1a schema:name Springer Nature - SN SciGraph project
41 rdf:type schema:Organization
42 N5851d02d948f4cd3b2111f5ae9174ed6 rdf:first sg:person.010647660001.34
43 rdf:rest rdf:nil
44 N6790fb73be29411f966fb182cbedf1d6 schema:issueNumber 11
45 rdf:type schema:PublicationIssue
46 N6af1645b03454a0fa4a773a75638198a schema:name dimensions_id
47 schema:value pub.1008294832
48 rdf:type schema:PropertyValue
49 Na7a5e9830ce54fe395cf2fc5e2085ff3 schema:name doi
50 schema:value 10.1007/bf00532076
51 rdf:type schema:PropertyValue
52 Nf88373aec8b440d68b5b5d8d1d0bac52 rdf:first sg:person.010476772135.01
53 rdf:rest N5851d02d948f4cd3b2111f5ae9174ed6
54 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
55 schema:name Chemical Sciences
56 rdf:type schema:DefinedTerm
57 anzsrc-for:0305 schema:inDefinedTermSet anzsrc-for:
58 schema:name Organic Chemistry
59 rdf:type schema:DefinedTerm
60 sg:journal.1358699 schema:issn 0132-6244
61 1573-8353
62 schema:name Chemistry of Heterocyclic Compounds
63 schema:publisher Springer Nature
64 rdf:type schema:Periodical
65 sg:person.010476772135.01 schema:affiliation grid-institutes:grid.419209.7
66 schema:familyName Ayupova
67 schema:givenName A. T.
68 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010476772135.01
69 rdf:type schema:Person
70 sg:person.010647660001.34 schema:affiliation grid-institutes:grid.419209.7
71 schema:familyName Galust'yan
72 schema:givenName G. G.
73 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010647660001.34
74 rdf:type schema:Person
75 sg:person.012433102130.12 schema:affiliation grid-institutes:grid.419209.7
76 schema:familyName Shevchenko
77 schema:givenName O. K.
78 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012433102130.12
79 rdf:type schema:Person
80 grid-institutes:grid.419209.7 schema:alternateName Institute for the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, 700170, Tashkent
81 schema:name Institute for the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, 700170, Tashkent
82 rdf:type schema:Organization
 




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


...