Synthesis of N-ferrocenylalkylated pyrazole derivatives View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2014-10

AUTHORS

E. Yu. Osipova, A. N. Rodionov, D. E. Arkhipov, M. M. Il’in, A. A. Simenel

ABSTRACT

Carbonyl derivatives of N-ferrocenyl alkyl pyrazoles were synthesized. The techniques of analytical separation of racemates of the synthesized compounds were developed. The structures of three compounds were determined by X-ray diffraction analysis.

PAGES

2285-2289

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-014-0736-y

DOI

http://dx.doi.org/10.1007/s11172-014-0736-y

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1043870335


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/2008/0301", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Analytical Chemistry", 
        "type": "DefinedTerm"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 119991, 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, 119991, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Osipova", 
        "givenName": "E. Yu.", 
        "id": "sg:person.014241577207.10", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014241577207.10"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 119991, 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, 119991, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Rodionov", 
        "givenName": "A. N.", 
        "id": "sg:person.016212142456.86", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016212142456.86"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "N. I. Pirogov Russian National Research Medical University, 1 ul. Ostrovityanova, 117997, Moscow, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.78028.35", 
          "name": [
            "A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 119991, Moscow, Russian Federation", 
            "N. I. Pirogov Russian National Research Medical University, 1 ul. Ostrovityanova, 117997, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Arkhipov", 
        "givenName": "D. E.", 
        "id": "sg:person.014441433661.39", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014441433661.39"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 119991, 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, 119991, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Il\u2019in", 
        "givenName": "M. M.", 
        "id": "sg:person.015661113163.01", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015661113163.01"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "National University of Science and Technology MISiS, 4 Leninskii prosp., 119991, Moscow, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.35043.31", 
          "name": [
            "A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 119991, Moscow, Russian Federation", 
            "National University of Science and Technology MISiS, 4 Leninskii prosp., 119991, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Simenel", 
        "givenName": "A. A.", 
        "id": "sg:person.014345475757.92", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014345475757.92"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "sg:pub.10.1007/s11172-014-0390-4", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1003271293", 
          "https://doi.org/10.1007/s11172-014-0390-4"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s11172-013-0298-4", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1052926095", 
          "https://doi.org/10.1007/s11172-013-0298-4"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s11172-010-0377-8", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1030181574", 
          "https://doi.org/10.1007/s11172-010-0377-8"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2014-10", 
    "datePublishedReg": "2014-10-01", 
    "description": "Carbonyl derivatives of N-ferrocenyl alkyl pyrazoles were synthesized. The techniques of analytical separation of racemates of the synthesized compounds were developed. The structures of three compounds were determined by X-ray diffraction analysis.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/s11172-014-0736-y", 
    "inLanguage": "en", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1022309", 
        "issn": [
          "1026-3500", 
          "1066-5285"
        ], 
        "name": "Russian Chemical Bulletin", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "10", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "63"
      }
    ], 
    "keywords": [
      "ray diffraction analysis", 
      "analytical separation", 
      "carbonyl derivatives", 
      "pyrazole derivatives", 
      "alkyl pyrazoles", 
      "diffraction analysis", 
      "compounds", 
      "derivatives", 
      "pyrazole", 
      "racemate", 
      "synthesis", 
      "separation", 
      "structure", 
      "technique", 
      "analysis"
    ], 
    "name": "Synthesis of N-ferrocenylalkylated pyrazole derivatives", 
    "pagination": "2285-2289", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1043870335"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s11172-014-0736-y"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s11172-014-0736-y", 
      "https://app.dimensions.ai/details/publication/pub.1043870335"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-06-01T22:13", 
    "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_637.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/s11172-014-0736-y"
  }
]
 

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/s11172-014-0736-y'

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/s11172-014-0736-y'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s11172-014-0736-y'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s11172-014-0736-y'


 

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

121 TRIPLES      22 PREDICATES      44 URIs      33 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s11172-014-0736-y schema:about anzsrc-for:03
2 anzsrc-for:0301
3 schema:author Ncf1c2d497e604721a5fa324e46f8d1d1
4 schema:citation sg:pub.10.1007/s11172-010-0377-8
5 sg:pub.10.1007/s11172-013-0298-4
6 sg:pub.10.1007/s11172-014-0390-4
7 schema:datePublished 2014-10
8 schema:datePublishedReg 2014-10-01
9 schema:description Carbonyl derivatives of N-ferrocenyl alkyl pyrazoles were synthesized. The techniques of analytical separation of racemates of the synthesized compounds were developed. The structures of three compounds were determined by X-ray diffraction analysis.
10 schema:genre article
11 schema:inLanguage en
12 schema:isAccessibleForFree false
13 schema:isPartOf N256babf65c9c449ba8cf09c427741e48
14 N31b011a00c364495a75f51500f28edb3
15 sg:journal.1022309
16 schema:keywords alkyl pyrazoles
17 analysis
18 analytical separation
19 carbonyl derivatives
20 compounds
21 derivatives
22 diffraction analysis
23 pyrazole
24 pyrazole derivatives
25 racemate
26 ray diffraction analysis
27 separation
28 structure
29 synthesis
30 technique
31 schema:name Synthesis of N-ferrocenylalkylated pyrazole derivatives
32 schema:pagination 2285-2289
33 schema:productId N32a9053aefd24edea4017238dd7efec3
34 Ne9ead5e0c75d4330b9253ed24f5af572
35 schema:sameAs https://app.dimensions.ai/details/publication/pub.1043870335
36 https://doi.org/10.1007/s11172-014-0736-y
37 schema:sdDatePublished 2022-06-01T22:13
38 schema:sdLicense https://scigraph.springernature.com/explorer/license/
39 schema:sdPublisher Nedeb3faeae0e4a409ee40078db002984
40 schema:url https://doi.org/10.1007/s11172-014-0736-y
41 sgo:license sg:explorer/license/
42 sgo:sdDataset articles
43 rdf:type schema:ScholarlyArticle
44 N10d246f2fda24a9aab8092802c1e7e16 rdf:first sg:person.014345475757.92
45 rdf:rest rdf:nil
46 N256babf65c9c449ba8cf09c427741e48 schema:volumeNumber 63
47 rdf:type schema:PublicationVolume
48 N2ab9a984b9014844a69ac32ad691d9da rdf:first sg:person.016212142456.86
49 rdf:rest N5516cdeb6bdd4766ab8b2e4b04ee7c82
50 N31b011a00c364495a75f51500f28edb3 schema:issueNumber 10
51 rdf:type schema:PublicationIssue
52 N32a9053aefd24edea4017238dd7efec3 schema:name doi
53 schema:value 10.1007/s11172-014-0736-y
54 rdf:type schema:PropertyValue
55 N5516cdeb6bdd4766ab8b2e4b04ee7c82 rdf:first sg:person.014441433661.39
56 rdf:rest Nef631c0a75264589bd321635f59d4e43
57 Ncf1c2d497e604721a5fa324e46f8d1d1 rdf:first sg:person.014241577207.10
58 rdf:rest N2ab9a984b9014844a69ac32ad691d9da
59 Ne9ead5e0c75d4330b9253ed24f5af572 schema:name dimensions_id
60 schema:value pub.1043870335
61 rdf:type schema:PropertyValue
62 Nedeb3faeae0e4a409ee40078db002984 schema:name Springer Nature - SN SciGraph project
63 rdf:type schema:Organization
64 Nef631c0a75264589bd321635f59d4e43 rdf:first sg:person.015661113163.01
65 rdf:rest N10d246f2fda24a9aab8092802c1e7e16
66 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
67 schema:name Chemical Sciences
68 rdf:type schema:DefinedTerm
69 anzsrc-for:0301 schema:inDefinedTermSet anzsrc-for:
70 schema:name Analytical Chemistry
71 rdf:type schema:DefinedTerm
72 sg:journal.1022309 schema:issn 1026-3500
73 1066-5285
74 schema:name Russian Chemical Bulletin
75 schema:publisher Springer Nature
76 rdf:type schema:Periodical
77 sg:person.014241577207.10 schema:affiliation grid-institutes:grid.431939.5
78 schema:familyName Osipova
79 schema:givenName E. Yu.
80 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014241577207.10
81 rdf:type schema:Person
82 sg:person.014345475757.92 schema:affiliation grid-institutes:grid.35043.31
83 schema:familyName Simenel
84 schema:givenName A. A.
85 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014345475757.92
86 rdf:type schema:Person
87 sg:person.014441433661.39 schema:affiliation grid-institutes:grid.78028.35
88 schema:familyName Arkhipov
89 schema:givenName D. E.
90 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014441433661.39
91 rdf:type schema:Person
92 sg:person.015661113163.01 schema:affiliation grid-institutes:grid.431939.5
93 schema:familyName Il’in
94 schema:givenName M. M.
95 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015661113163.01
96 rdf:type schema:Person
97 sg:person.016212142456.86 schema:affiliation grid-institutes:grid.431939.5
98 schema:familyName Rodionov
99 schema:givenName A. N.
100 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016212142456.86
101 rdf:type schema:Person
102 sg:pub.10.1007/s11172-010-0377-8 schema:sameAs https://app.dimensions.ai/details/publication/pub.1030181574
103 https://doi.org/10.1007/s11172-010-0377-8
104 rdf:type schema:CreativeWork
105 sg:pub.10.1007/s11172-013-0298-4 schema:sameAs https://app.dimensions.ai/details/publication/pub.1052926095
106 https://doi.org/10.1007/s11172-013-0298-4
107 rdf:type schema:CreativeWork
108 sg:pub.10.1007/s11172-014-0390-4 schema:sameAs https://app.dimensions.ai/details/publication/pub.1003271293
109 https://doi.org/10.1007/s11172-014-0390-4
110 rdf:type schema:CreativeWork
111 grid-institutes:grid.35043.31 schema:alternateName National University of Science and Technology MISiS, 4 Leninskii prosp., 119991, Moscow, Russian Federation
112 schema:name A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 119991, Moscow, Russian Federation
113 National University of Science and Technology MISiS, 4 Leninskii prosp., 119991, Moscow, Russian Federation
114 rdf:type schema:Organization
115 grid-institutes:grid.431939.5 schema:alternateName A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 119991, Moscow, Russian Federation
116 schema:name A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 119991, Moscow, Russian Federation
117 rdf:type schema:Organization
118 grid-institutes:grid.78028.35 schema:alternateName N. I. Pirogov Russian National Research Medical University, 1 ul. Ostrovityanova, 117997, Moscow, Russian Federation
119 schema:name A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 119991, Moscow, Russian Federation
120 N. I. Pirogov Russian National Research Medical University, 1 ul. Ostrovityanova, 117997, Moscow, Russian Federation
121 rdf:type schema:Organization
 




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


...