Reactions of polychlorophenyllithium compounds with electrophiles View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2005-04

AUTHORS

A. S. Burukin, A. A. Vasil'ev, M. I. Struchkova, V. V. Kachala, S. G. Zlotin

ABSTRACT

Polychloroaromatic compounds lithiated by BunLi in THF react with several electrophilic agents of which aldehydes and epoxides seem to be the most promising from the preparative point of view.

PAGES

964-969

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-005-0341-1

DOI

http://dx.doi.org/10.1007/s11172-005-0341-1

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1019500692


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"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.439283.7", 
          "name": [
            "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Burukin", 
        "givenName": "A. S.", 
        "id": "sg:person.016176063647.02", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016176063647.02"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.439283.7", 
          "name": [
            "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Vasil'ev", 
        "givenName": "A. A.", 
        "id": "sg:person.011652651152.04", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011652651152.04"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.439283.7", 
          "name": [
            "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Struchkova", 
        "givenName": "M. I.", 
        "id": "sg:person.01342454222.91", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01342454222.91"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.439283.7", 
          "name": [
            "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Kachala", 
        "givenName": "V. V.", 
        "id": "sg:person.0702615023.01", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0702615023.01"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.439283.7", 
          "name": [
            "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Zlotin", 
        "givenName": "S. G.", 
        "id": "sg:person.011575424313.47", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011575424313.47"
        ], 
        "type": "Person"
      }
    ], 
    "datePublished": "2005-04", 
    "datePublishedReg": "2005-04-01", 
    "description": "Polychloroaromatic compounds lithiated by BunLi in THF react with several electrophilic agents of which aldehydes and epoxides seem to be the most promising from the preparative point of view.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/s11172-005-0341-1", 
    "inLanguage": "en", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1022309", 
        "issn": [
          "1026-3500", 
          "1066-5285"
        ], 
        "name": "Russian Chemical Bulletin", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "4", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "54"
      }
    ], 
    "keywords": [
      "preparative point", 
      "THF reacts", 
      "polychloroaromatic compounds", 
      "electrophilic agents", 
      "compounds", 
      "BunLi", 
      "electrophiles", 
      "aldehydes", 
      "epoxides", 
      "reacts", 
      "reaction", 
      "agents", 
      "point", 
      "view"
    ], 
    "name": "Reactions of polychlorophenyllithium compounds with electrophiles", 
    "pagination": "964-969", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1019500692"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s11172-005-0341-1"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s11172-005-0341-1", 
      "https://app.dimensions.ai/details/publication/pub.1019500692"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-06-01T22:03", 
    "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_403.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/s11172-005-0341-1"
  }
]
 

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/s11172-005-0341-1'

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/s11172-005-0341-1'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s11172-005-0341-1'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s11172-005-0341-1'


 

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

96 TRIPLES      21 PREDICATES      39 URIs      32 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s11172-005-0341-1 schema:about anzsrc-for:03
2 schema:author N05d55a1bc9824d52b886b779e53c2f72
3 schema:datePublished 2005-04
4 schema:datePublishedReg 2005-04-01
5 schema:description Polychloroaromatic compounds lithiated by BunLi in THF react with several electrophilic agents of which aldehydes and epoxides seem to be the most promising from the preparative point of view.
6 schema:genre article
7 schema:inLanguage en
8 schema:isAccessibleForFree false
9 schema:isPartOf N9da095d574394675a7188dc6b7b94727
10 Nd34dc07b978145c991a2312d20de9dce
11 sg:journal.1022309
12 schema:keywords BunLi
13 THF reacts
14 agents
15 aldehydes
16 compounds
17 electrophiles
18 electrophilic agents
19 epoxides
20 point
21 polychloroaromatic compounds
22 preparative point
23 reaction
24 reacts
25 view
26 schema:name Reactions of polychlorophenyllithium compounds with electrophiles
27 schema:pagination 964-969
28 schema:productId N767e5e97253249ecad297d9c57faf700
29 Ned54b82c0a77430a8e86fde2a6c8a2f5
30 schema:sameAs https://app.dimensions.ai/details/publication/pub.1019500692
31 https://doi.org/10.1007/s11172-005-0341-1
32 schema:sdDatePublished 2022-06-01T22:03
33 schema:sdLicense https://scigraph.springernature.com/explorer/license/
34 schema:sdPublisher N130bc52553974f119650ff7452c3fbd0
35 schema:url https://doi.org/10.1007/s11172-005-0341-1
36 sgo:license sg:explorer/license/
37 sgo:sdDataset articles
38 rdf:type schema:ScholarlyArticle
39 N05d55a1bc9824d52b886b779e53c2f72 rdf:first sg:person.016176063647.02
40 rdf:rest N6c4733148dce409987820446521c3271
41 N0671f309cfaf43dd8f114b0103c4cefe rdf:first sg:person.01342454222.91
42 rdf:rest N49d7947dfee747b1824eb5bf3726d6b2
43 N130bc52553974f119650ff7452c3fbd0 schema:name Springer Nature - SN SciGraph project
44 rdf:type schema:Organization
45 N49d7947dfee747b1824eb5bf3726d6b2 rdf:first sg:person.0702615023.01
46 rdf:rest Ne1bd3645933649759f1881af046dd828
47 N6c4733148dce409987820446521c3271 rdf:first sg:person.011652651152.04
48 rdf:rest N0671f309cfaf43dd8f114b0103c4cefe
49 N767e5e97253249ecad297d9c57faf700 schema:name dimensions_id
50 schema:value pub.1019500692
51 rdf:type schema:PropertyValue
52 N9da095d574394675a7188dc6b7b94727 schema:volumeNumber 54
53 rdf:type schema:PublicationVolume
54 Nd34dc07b978145c991a2312d20de9dce schema:issueNumber 4
55 rdf:type schema:PublicationIssue
56 Ne1bd3645933649759f1881af046dd828 rdf:first sg:person.011575424313.47
57 rdf:rest rdf:nil
58 Ned54b82c0a77430a8e86fde2a6c8a2f5 schema:name doi
59 schema:value 10.1007/s11172-005-0341-1
60 rdf:type schema:PropertyValue
61 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
62 schema:name Chemical Sciences
63 rdf:type schema:DefinedTerm
64 sg:journal.1022309 schema:issn 1026-3500
65 1066-5285
66 schema:name Russian Chemical Bulletin
67 schema:publisher Springer Nature
68 rdf:type schema:Periodical
69 sg:person.011575424313.47 schema:affiliation grid-institutes:grid.439283.7
70 schema:familyName Zlotin
71 schema:givenName S. G.
72 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011575424313.47
73 rdf:type schema:Person
74 sg:person.011652651152.04 schema:affiliation grid-institutes:grid.439283.7
75 schema:familyName Vasil'ev
76 schema:givenName A. A.
77 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011652651152.04
78 rdf:type schema:Person
79 sg:person.01342454222.91 schema:affiliation grid-institutes:grid.439283.7
80 schema:familyName Struchkova
81 schema:givenName M. I.
82 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01342454222.91
83 rdf:type schema:Person
84 sg:person.016176063647.02 schema:affiliation grid-institutes:grid.439283.7
85 schema:familyName Burukin
86 schema:givenName A. S.
87 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016176063647.02
88 rdf:type schema:Person
89 sg:person.0702615023.01 schema:affiliation grid-institutes:grid.439283.7
90 schema:familyName Kachala
91 schema:givenName V. V.
92 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0702615023.01
93 rdf:type schema:Person
94 grid-institutes:grid.439283.7 schema:alternateName N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation
95 schema:name N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation
96 rdf:type schema:Organization
 




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


...