Five-Membered 2,3-Dioxo Heterocycles: LXXI.* Recyclization of 4,5-Diaroyl-1H-pyrrole-2,3-diones by the Action of Substituted Hydrazines. Crystalline and Molecular Structure of 2-(3-Benzoyl- 1-benzyl-5-phenyl-1H-pyrazol-4-yl)-N-(4-methoxyphenyl)- ... View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2010-10

AUTHORS

P. S. Silaichev, N. V. Kudrevatykh, Z. G. Aliev, A. N. Maslivets

ABSTRACT

1-Aryl-4,5-diaroyl-1H-pyrrole-2,3-diones reacted with benzyl- and phenylhydrazines to give N-aryl-2-(5-aryl-3-aroyl-1-benzyl(phenyl)-1H-pyrazol-4-yl)-2-oxoacetamides whose structure was proved by X-ray analysis.

PAGES

1546-1549

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070428010100180

DOI

http://dx.doi.org/10.1134/s1070428010100180

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1000922346


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/2008/0306", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Physical Chemistry (incl. Structural)", 
        "type": "DefinedTerm"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "Institute of Natural Sciences, Perm State University, ul., Genkelya 4, 614990, Perm, Russia", 
          "id": "http://www.grid.ac/institutes/grid.77611.36", 
          "name": [
            "Institute of Natural Sciences, Perm State University, ul., Genkelya 4, 614990, Perm, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Silaichev", 
        "givenName": "P. S.", 
        "id": "sg:person.015746074244.34", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015746074244.34"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Perm State University, ul., Bukireva 15, 614990, Perm, Russia", 
          "id": "http://www.grid.ac/institutes/grid.77611.36", 
          "name": [
            "Perm State University, ul., Bukireva 15, 614990, Perm, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Kudrevatykh", 
        "givenName": "N. V.", 
        "id": "sg:person.014020361713.92", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014020361713.92"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Chemical Physics Problems, Russian Academy of Sciences, Chernogolovka, Moscow oblast, Russia", 
          "id": "http://www.grid.ac/institutes/grid.418949.9", 
          "name": [
            "Institute of Chemical Physics Problems, Russian Academy of Sciences, Chernogolovka, Moscow oblast, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Aliev", 
        "givenName": "Z. G.", 
        "id": "sg:person.010574144735.96", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010574144735.96"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Perm State University, ul., Bukireva 15, 614990, Perm, Russia", 
          "id": "http://www.grid.ac/institutes/grid.77611.36", 
          "name": [
            "Institute of Natural Sciences, Perm State University, ul., Genkelya 4, 614990, Perm, Russia", 
            "Perm State University, ul., Bukireva 15, 614990, Perm, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Maslivets", 
        "givenName": "A. N.", 
        "id": "sg:person.0662414002.02", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0662414002.02"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "sg:pub.10.1134/s1070428010060278", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1022768081", 
          "https://doi.org/10.1134/s1070428010060278"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2010-10", 
    "datePublishedReg": "2010-10-01", 
    "description": "Abstract1-Aryl-4,5-diaroyl-1H-pyrrole-2,3-diones reacted with benzyl- and phenylhydrazines to give N-aryl-2-(5-aryl-3-aroyl-1-benzyl(phenyl)-1H-pyrazol-4-yl)-2-oxoacetamides whose structure was proved by X-ray analysis.", 
    "genre": "article", 
    "id": "sg:pub.10.1134/s1070428010100180", 
    "inLanguage": "en", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1136317", 
        "issn": [
          "0514-7492", 
          "1070-4280"
        ], 
        "name": "Russian Journal of Organic Chemistry", 
        "publisher": "Pleiades Publishing", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "10", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "46"
      }
    ], 
    "keywords": [
      "molecular structure", 
      "substituted hydrazines", 
      "Five-Membered", 
      "ray analysis", 
      "heterocycles", 
      "hydrazine", 
      "benzyl", 
      "structure", 
      "recyclization", 
      "phenylhydrazine", 
      "LXXI", 
      "analysis", 
      "action"
    ], 
    "name": "Five-Membered 2,3-Dioxo Heterocycles: LXXI.* Recyclization of 4,5-Diaroyl-1H-pyrrole-2,3-diones by the Action of Substituted Hydrazines. Crystalline and Molecular Structure of 2-(3-Benzoyl- 1-benzyl-5-phenyl-1H-pyrazol-4-yl)-N-(4-methoxyphenyl)- 2-oxoacetamide", 
    "pagination": "1546-1549", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1000922346"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1134/s1070428010100180"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1134/s1070428010100180", 
      "https://app.dimensions.ai/details/publication/pub.1000922346"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-01-01T18:22", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20220101/entities/gbq_results/article/article_506.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1134/s1070428010100180"
  }
]
 

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/s1070428010100180'

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/s1070428010100180'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1134/s1070428010100180'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1134/s1070428010100180'


 

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

101 TRIPLES      22 PREDICATES      40 URIs      31 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1134/s1070428010100180 schema:about anzsrc-for:03
2 anzsrc-for:0306
3 schema:author N0440b10dfe4245be9c0f02ed3dd25297
4 schema:citation sg:pub.10.1134/s1070428010060278
5 schema:datePublished 2010-10
6 schema:datePublishedReg 2010-10-01
7 schema:description Abstract1-Aryl-4,5-diaroyl-1H-pyrrole-2,3-diones reacted with benzyl- and phenylhydrazines to give N-aryl-2-(5-aryl-3-aroyl-1-benzyl(phenyl)-1H-pyrazol-4-yl)-2-oxoacetamides whose structure was proved by X-ray analysis.
8 schema:genre article
9 schema:inLanguage en
10 schema:isAccessibleForFree false
11 schema:isPartOf N554816216eae4ec798217f9a2f74a2eb
12 N7e9ea46e125348398f4a99908da9cfa3
13 sg:journal.1136317
14 schema:keywords Five-Membered
15 LXXI
16 action
17 analysis
18 benzyl
19 heterocycles
20 hydrazine
21 molecular structure
22 phenylhydrazine
23 ray analysis
24 recyclization
25 structure
26 substituted hydrazines
27 schema:name Five-Membered 2,3-Dioxo Heterocycles: LXXI.* Recyclization of 4,5-Diaroyl-1H-pyrrole-2,3-diones by the Action of Substituted Hydrazines. Crystalline and Molecular Structure of 2-(3-Benzoyl- 1-benzyl-5-phenyl-1H-pyrazol-4-yl)-N-(4-methoxyphenyl)- 2-oxoacetamide
28 schema:pagination 1546-1549
29 schema:productId N8eed877aaf4d4b0691495b129c6d14c1
30 Ne9b414b9ff0b43249c553f4464dd12a7
31 schema:sameAs https://app.dimensions.ai/details/publication/pub.1000922346
32 https://doi.org/10.1134/s1070428010100180
33 schema:sdDatePublished 2022-01-01T18:22
34 schema:sdLicense https://scigraph.springernature.com/explorer/license/
35 schema:sdPublisher N340b41b3e3674bd19d2eabd367a14d40
36 schema:url https://doi.org/10.1134/s1070428010100180
37 sgo:license sg:explorer/license/
38 sgo:sdDataset articles
39 rdf:type schema:ScholarlyArticle
40 N0440b10dfe4245be9c0f02ed3dd25297 rdf:first sg:person.015746074244.34
41 rdf:rest N26d0045f4d334b688ac91da4c9d20399
42 N26d0045f4d334b688ac91da4c9d20399 rdf:first sg:person.014020361713.92
43 rdf:rest N47e01911f54240bf9a3ebef624192359
44 N340b41b3e3674bd19d2eabd367a14d40 schema:name Springer Nature - SN SciGraph project
45 rdf:type schema:Organization
46 N4389df05b5f444948fa459f68cd3b6e3 rdf:first sg:person.0662414002.02
47 rdf:rest rdf:nil
48 N47e01911f54240bf9a3ebef624192359 rdf:first sg:person.010574144735.96
49 rdf:rest N4389df05b5f444948fa459f68cd3b6e3
50 N554816216eae4ec798217f9a2f74a2eb schema:issueNumber 10
51 rdf:type schema:PublicationIssue
52 N7e9ea46e125348398f4a99908da9cfa3 schema:volumeNumber 46
53 rdf:type schema:PublicationVolume
54 N8eed877aaf4d4b0691495b129c6d14c1 schema:name dimensions_id
55 schema:value pub.1000922346
56 rdf:type schema:PropertyValue
57 Ne9b414b9ff0b43249c553f4464dd12a7 schema:name doi
58 schema:value 10.1134/s1070428010100180
59 rdf:type schema:PropertyValue
60 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
61 schema:name Chemical Sciences
62 rdf:type schema:DefinedTerm
63 anzsrc-for:0306 schema:inDefinedTermSet anzsrc-for:
64 schema:name Physical Chemistry (incl. Structural)
65 rdf:type schema:DefinedTerm
66 sg:journal.1136317 schema:issn 0514-7492
67 1070-4280
68 schema:name Russian Journal of Organic Chemistry
69 schema:publisher Pleiades Publishing
70 rdf:type schema:Periodical
71 sg:person.010574144735.96 schema:affiliation grid-institutes:grid.418949.9
72 schema:familyName Aliev
73 schema:givenName Z. G.
74 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010574144735.96
75 rdf:type schema:Person
76 sg:person.014020361713.92 schema:affiliation grid-institutes:grid.77611.36
77 schema:familyName Kudrevatykh
78 schema:givenName N. V.
79 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014020361713.92
80 rdf:type schema:Person
81 sg:person.015746074244.34 schema:affiliation grid-institutes:grid.77611.36
82 schema:familyName Silaichev
83 schema:givenName P. S.
84 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015746074244.34
85 rdf:type schema:Person
86 sg:person.0662414002.02 schema:affiliation grid-institutes:grid.77611.36
87 schema:familyName Maslivets
88 schema:givenName A. N.
89 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0662414002.02
90 rdf:type schema:Person
91 sg:pub.10.1134/s1070428010060278 schema:sameAs https://app.dimensions.ai/details/publication/pub.1022768081
92 https://doi.org/10.1134/s1070428010060278
93 rdf:type schema:CreativeWork
94 grid-institutes:grid.418949.9 schema:alternateName Institute of Chemical Physics Problems, Russian Academy of Sciences, Chernogolovka, Moscow oblast, Russia
95 schema:name Institute of Chemical Physics Problems, Russian Academy of Sciences, Chernogolovka, Moscow oblast, Russia
96 rdf:type schema:Organization
97 grid-institutes:grid.77611.36 schema:alternateName Institute of Natural Sciences, Perm State University, ul., Genkelya 4, 614990, Perm, Russia
98 Perm State University, ul., Bukireva 15, 614990, Perm, Russia
99 schema:name Institute of Natural Sciences, Perm State University, ul., Genkelya 4, 614990, Perm, Russia
100 Perm State University, ul., Bukireva 15, 614990, Perm, Russia
101 rdf:type schema:Organization
 




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


...