Simple synthesis of 2-[5-substituted-4-(trichloroacetyl)-1H-pyrazole-3-carbonyloxy]benzoic acids View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2019-03

AUTHORS

N. Yu. Lisovenko, E. R. Nasibullina, M. V. Dmitriev

ABSTRACT

A simple method for the synthesis of 2-(5-substituted-4-(trichloroacetyl)-1H-pyrazole-3-carbonyloxy)benzoic acids was suggested based on a tandem reaction of 5-substituted 4-trichloroacetylfuran-2,3-diones and salicylic acid hydrazide.

PAGES

578-582

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-019-2457-8

DOI

http://dx.doi.org/10.1007/s11172-019-2457-8

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1113834124


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": "Perm State National Research University, 15 ul. Bukireva, 614990, Perm, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.77611.36", 
          "name": [
            "Perm State National Research University, 15 ul. Bukireva, 614990, Perm, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Lisovenko", 
        "givenName": "N. Yu.", 
        "id": "sg:person.013246751157.06", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013246751157.06"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Perm State National Research University, 15 ul. Bukireva, 614990, Perm, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.77611.36", 
          "name": [
            "Perm State National Research University, 15 ul. Bukireva, 614990, Perm, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Nasibullina", 
        "givenName": "E. R.", 
        "id": "sg:person.07542410014.89", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07542410014.89"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Perm State National Research University, 15 ul. Bukireva, 614990, Perm, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.77611.36", 
          "name": [
            "Perm State National Research University, 15 ul. Bukireva, 614990, Perm, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Dmitriev", 
        "givenName": "M. V.", 
        "id": "sg:person.015741240313.37", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015741240313.37"
        ], 
        "type": "Person"
      }
    ], 
    "datePublished": "2019-03", 
    "datePublishedReg": "2019-03-01", 
    "description": "A simple method for the synthesis of 2-(5-substituted-4-(trichloroacetyl)-1H-pyrazole-3-carbonyloxy)benzoic acids was suggested based on a tandem reaction of 5-substituted 4-trichloroacetylfuran-2,3-diones and salicylic acid hydrazide.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/s11172-019-2457-8", 
    "inLanguage": "en", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1022309", 
        "issn": [
          "1026-3500", 
          "1066-5285"
        ], 
        "name": "Russian Chemical Bulletin", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "3", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "68"
      }
    ], 
    "keywords": [
      "pyrazole-3", 
      "salicylic acid hydrazide", 
      "simple synthesis", 
      "tandem reaction", 
      "acid hydrazide", 
      "synthesis", 
      "simple method", 
      "acid", 
      "hydrazide", 
      "dione", 
      "reaction", 
      "method"
    ], 
    "name": "Simple synthesis of 2-[5-substituted-4-(trichloroacetyl)-1H-pyrazole-3-carbonyloxy]benzoic acids", 
    "pagination": "578-582", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1113834124"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s11172-019-2457-8"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s11172-019-2457-8", 
      "https://app.dimensions.ai/details/publication/pub.1113834124"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-06-01T22:19", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20220601/entities/gbq_results/article/article_804.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/s11172-019-2457-8"
  }
]
 

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/s11172-019-2457-8'

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/s11172-019-2457-8'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s11172-019-2457-8'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s11172-019-2457-8'


 

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

84 TRIPLES      21 PREDICATES      38 URIs      30 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s11172-019-2457-8 schema:about anzsrc-for:03
2 anzsrc-for:0305
3 schema:author N11e3249053d34a1fa331cea7578d4b74
4 schema:datePublished 2019-03
5 schema:datePublishedReg 2019-03-01
6 schema:description A simple method for the synthesis of 2-(5-substituted-4-(trichloroacetyl)-1H-pyrazole-3-carbonyloxy)benzoic acids was suggested based on a tandem reaction of 5-substituted 4-trichloroacetylfuran-2,3-diones and salicylic acid hydrazide.
7 schema:genre article
8 schema:inLanguage en
9 schema:isAccessibleForFree false
10 schema:isPartOf Nc92a64811943499aa41cb58a87520567
11 Ndb58399b0d6e40aa9b211ef2f8fb985e
12 sg:journal.1022309
13 schema:keywords acid
14 acid hydrazide
15 dione
16 hydrazide
17 method
18 pyrazole-3
19 reaction
20 salicylic acid hydrazide
21 simple method
22 simple synthesis
23 synthesis
24 tandem reaction
25 schema:name Simple synthesis of 2-[5-substituted-4-(trichloroacetyl)-1H-pyrazole-3-carbonyloxy]benzoic acids
26 schema:pagination 578-582
27 schema:productId Nd32a856b40904f00b63953c41d814bed
28 Nf7028d9f591e4a828c041578f09b0513
29 schema:sameAs https://app.dimensions.ai/details/publication/pub.1113834124
30 https://doi.org/10.1007/s11172-019-2457-8
31 schema:sdDatePublished 2022-06-01T22:19
32 schema:sdLicense https://scigraph.springernature.com/explorer/license/
33 schema:sdPublisher N0ecdaa8146bc43f5938682014c421bfd
34 schema:url https://doi.org/10.1007/s11172-019-2457-8
35 sgo:license sg:explorer/license/
36 sgo:sdDataset articles
37 rdf:type schema:ScholarlyArticle
38 N0ecdaa8146bc43f5938682014c421bfd schema:name Springer Nature - SN SciGraph project
39 rdf:type schema:Organization
40 N11e3249053d34a1fa331cea7578d4b74 rdf:first sg:person.013246751157.06
41 rdf:rest Nf5afa7cc0250469c8404670dfdf5db17
42 Nb5e84ccd58184b0cad0d1e6f03a26d40 rdf:first sg:person.015741240313.37
43 rdf:rest rdf:nil
44 Nc92a64811943499aa41cb58a87520567 schema:volumeNumber 68
45 rdf:type schema:PublicationVolume
46 Nd32a856b40904f00b63953c41d814bed schema:name doi
47 schema:value 10.1007/s11172-019-2457-8
48 rdf:type schema:PropertyValue
49 Ndb58399b0d6e40aa9b211ef2f8fb985e schema:issueNumber 3
50 rdf:type schema:PublicationIssue
51 Nf5afa7cc0250469c8404670dfdf5db17 rdf:first sg:person.07542410014.89
52 rdf:rest Nb5e84ccd58184b0cad0d1e6f03a26d40
53 Nf7028d9f591e4a828c041578f09b0513 schema:name dimensions_id
54 schema:value pub.1113834124
55 rdf:type schema:PropertyValue
56 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
57 schema:name Chemical Sciences
58 rdf:type schema:DefinedTerm
59 anzsrc-for:0305 schema:inDefinedTermSet anzsrc-for:
60 schema:name Organic Chemistry
61 rdf:type schema:DefinedTerm
62 sg:journal.1022309 schema:issn 1026-3500
63 1066-5285
64 schema:name Russian Chemical Bulletin
65 schema:publisher Springer Nature
66 rdf:type schema:Periodical
67 sg:person.013246751157.06 schema:affiliation grid-institutes:grid.77611.36
68 schema:familyName Lisovenko
69 schema:givenName N. Yu.
70 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013246751157.06
71 rdf:type schema:Person
72 sg:person.015741240313.37 schema:affiliation grid-institutes:grid.77611.36
73 schema:familyName Dmitriev
74 schema:givenName M. V.
75 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015741240313.37
76 rdf:type schema:Person
77 sg:person.07542410014.89 schema:affiliation grid-institutes:grid.77611.36
78 schema:familyName Nasibullina
79 schema:givenName E. R.
80 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07542410014.89
81 rdf:type schema:Person
82 grid-institutes:grid.77611.36 schema:alternateName Perm State National Research University, 15 ul. Bukireva, 614990, Perm, Russian Federation
83 schema:name Perm State National Research University, 15 ul. Bukireva, 614990, Perm, Russian Federation
84 rdf:type schema:Organization
 




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


...