Bis(tetrazolyl)benzenes as ligands in the Suzuki reaction: Promoters or inhibitors? View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2006-01

AUTHORS

A. S. Burukin, A. A. Vasil’ev, N. L. Merkulova, M. I. Struchkova, S. G. Zlotin

ABSTRACT

The Suzuki cross-coupling with phenylboronic acid in the presence of the Pd(OAc)2/K3PO4/DMF catalytic system was successful for aryl bromides and somewhat poorer for aryl chlorides. Addition of 1,3-bis(tetrazol-1-yl)benzene or its analogs lowered the yields of biaryls.

PAGES

118-122

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-006-0224-0

DOI

http://dx.doi.org/10.1007/s11172-006-0224-0

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1018872829


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\u2019ev", 
        "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": "ChemBridge Corporation, 1 ul. Malaya Pirogovskaya, 119435, Moscow, Russian Federation", 
          "id": "http://www.grid.ac/institutes/None", 
          "name": [
            "ChemBridge Corporation, 1 ul. Malaya Pirogovskaya, 119435, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Merkulova", 
        "givenName": "N. L.", 
        "id": "sg:person.012025226546.28", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012025226546.28"
        ], 
        "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": "Zlotin", 
        "givenName": "S. G.", 
        "id": "sg:person.07641341153.91", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07641341153.91"
        ], 
        "type": "Person"
      }
    ], 
    "datePublished": "2006-01", 
    "datePublishedReg": "2006-01-01", 
    "description": "The Suzuki cross-coupling with phenylboronic acid in the presence of the Pd(OAc)2/K3PO4/DMF catalytic system was successful for aryl bromides and somewhat poorer for aryl chlorides. Addition of 1,3-bis(tetrazol-1-yl)benzene or its analogs lowered the yields of biaryls.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/s11172-006-0224-0", 
    "inLanguage": "en", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1022309", 
        "issn": [
          "1026-3500", 
          "1066-5285"
        ], 
        "name": "Russian Chemical Bulletin", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "1", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "55"
      }
    ], 
    "keywords": [
      "inhibitors", 
      "acid", 
      "presence", 
      "promoter", 
      "addition", 
      "analogues", 
      "ligands", 
      "reaction", 
      "chloride", 
      "system", 
      "bromide", 
      "phenylboronic acid", 
      "yield", 
      "Suzuki", 
      "biaryls", 
      "Suzuki reaction", 
      "aryl bromides", 
      "catalytic system", 
      "aryl chlorides", 
      "yields of biaryls"
    ], 
    "name": "Bis(tetrazolyl)benzenes as ligands in the Suzuki reaction: Promoters or inhibitors?", 
    "pagination": "118-122", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1018872829"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s11172-006-0224-0"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s11172-006-0224-0", 
      "https://app.dimensions.ai/details/publication/pub.1018872829"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-05-10T09:57", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20220509/entities/gbq_results/article/article_424.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/s11172-006-0224-0"
  }
]
 

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/s11172-006-0224-0'

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/s11172-006-0224-0'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s11172-006-0224-0'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s11172-006-0224-0'


 

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

105 TRIPLES      21 PREDICATES      45 URIs      38 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s11172-006-0224-0 schema:about anzsrc-for:03
2 schema:author N29a9062a5b86435ea9d2447aefa58ce2
3 schema:datePublished 2006-01
4 schema:datePublishedReg 2006-01-01
5 schema:description The Suzuki cross-coupling with phenylboronic acid in the presence of the Pd(OAc)2/K3PO4/DMF catalytic system was successful for aryl bromides and somewhat poorer for aryl chlorides. Addition of 1,3-bis(tetrazol-1-yl)benzene or its analogs lowered the yields of biaryls.
6 schema:genre article
7 schema:inLanguage en
8 schema:isAccessibleForFree false
9 schema:isPartOf N925df4ce06c445b4ae5c3bbb338659a7
10 Nf455b8009f8849ef951c71d7737eeb62
11 sg:journal.1022309
12 schema:keywords Suzuki
13 Suzuki reaction
14 acid
15 addition
16 analogues
17 aryl bromides
18 aryl chlorides
19 biaryls
20 bromide
21 catalytic system
22 chloride
23 inhibitors
24 ligands
25 phenylboronic acid
26 presence
27 promoter
28 reaction
29 system
30 yield
31 yields of biaryls
32 schema:name Bis(tetrazolyl)benzenes as ligands in the Suzuki reaction: Promoters or inhibitors?
33 schema:pagination 118-122
34 schema:productId N53663e5f94ee422397a6ef94d2a38bf0
35 N61b1f32a511044a9bcabbeca1af99a4a
36 schema:sameAs https://app.dimensions.ai/details/publication/pub.1018872829
37 https://doi.org/10.1007/s11172-006-0224-0
38 schema:sdDatePublished 2022-05-10T09:57
39 schema:sdLicense https://scigraph.springernature.com/explorer/license/
40 schema:sdPublisher Nf5fd289bc5fe4bbfbff9160b273c1be5
41 schema:url https://doi.org/10.1007/s11172-006-0224-0
42 sgo:license sg:explorer/license/
43 sgo:sdDataset articles
44 rdf:type schema:ScholarlyArticle
45 N29a9062a5b86435ea9d2447aefa58ce2 rdf:first sg:person.016176063647.02
46 rdf:rest N5d9fcc3b01a84df7b2c00f70d3fd25ee
47 N4f0e4ca2668140c0954f551df13d8b40 rdf:first sg:person.01342454222.91
48 rdf:rest Necc914b6044e4fa3a95ce960adfc2835
49 N53663e5f94ee422397a6ef94d2a38bf0 schema:name dimensions_id
50 schema:value pub.1018872829
51 rdf:type schema:PropertyValue
52 N5d9fcc3b01a84df7b2c00f70d3fd25ee rdf:first sg:person.011652651152.04
53 rdf:rest Nbcbd3fd2937346a687b68cbf0e7b6f34
54 N61b1f32a511044a9bcabbeca1af99a4a schema:name doi
55 schema:value 10.1007/s11172-006-0224-0
56 rdf:type schema:PropertyValue
57 N925df4ce06c445b4ae5c3bbb338659a7 schema:issueNumber 1
58 rdf:type schema:PublicationIssue
59 Nbcbd3fd2937346a687b68cbf0e7b6f34 rdf:first sg:person.012025226546.28
60 rdf:rest N4f0e4ca2668140c0954f551df13d8b40
61 Necc914b6044e4fa3a95ce960adfc2835 rdf:first sg:person.07641341153.91
62 rdf:rest rdf:nil
63 Nf455b8009f8849ef951c71d7737eeb62 schema:volumeNumber 55
64 rdf:type schema:PublicationVolume
65 Nf5fd289bc5fe4bbfbff9160b273c1be5 schema:name Springer Nature - SN SciGraph project
66 rdf:type schema:Organization
67 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
68 schema:name Chemical Sciences
69 rdf:type schema:DefinedTerm
70 sg:journal.1022309 schema:issn 1026-3500
71 1066-5285
72 schema:name Russian Chemical Bulletin
73 schema:publisher Springer Nature
74 rdf:type schema:Periodical
75 sg:person.011652651152.04 schema:affiliation grid-institutes:grid.439283.7
76 schema:familyName Vasil’ev
77 schema:givenName A. A.
78 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011652651152.04
79 rdf:type schema:Person
80 sg:person.012025226546.28 schema:affiliation grid-institutes:None
81 schema:familyName Merkulova
82 schema:givenName N. L.
83 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012025226546.28
84 rdf:type schema:Person
85 sg:person.01342454222.91 schema:affiliation grid-institutes:grid.439283.7
86 schema:familyName Struchkova
87 schema:givenName M. I.
88 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01342454222.91
89 rdf:type schema:Person
90 sg:person.016176063647.02 schema:affiliation grid-institutes:grid.439283.7
91 schema:familyName Burukin
92 schema:givenName A. S.
93 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016176063647.02
94 rdf:type schema:Person
95 sg:person.07641341153.91 schema:affiliation grid-institutes:grid.439283.7
96 schema:familyName Zlotin
97 schema:givenName S. G.
98 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07641341153.91
99 rdf:type schema:Person
100 grid-institutes:None schema:alternateName ChemBridge Corporation, 1 ul. Malaya Pirogovskaya, 119435, Moscow, Russian Federation
101 schema:name ChemBridge Corporation, 1 ul. Malaya Pirogovskaya, 119435, Moscow, Russian Federation
102 rdf:type schema:Organization
103 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
104 schema:name N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation
105 rdf:type schema:Organization
 




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


...