Nitrogen-tellurium heterocycles View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1989-01

AUTHORS

I. D. Sadekov, G. M. Abakarov, A. A. Shneider, S. G. Kuren', A. G. Starikov, A. D. Garnovskii, V. I. Minkin

ABSTRACT

Several 2-substituted benzotellurazoles have been prepared by the reaction of N-allyl derivatives of o-methyltelluroaniline with POC13 or SOC12 followed by reduction of the σ-telluranes which are formed. The use of the zinc and sodium salts of o-aminotellurophenol and 2-chlorotellurenylazobenzene, in a procedure similar to that used to prepare benzothiazoles and benzoselenazoles, did not lead to the formation of benzotellurazoles. More... »

PAGES

103-108

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00472631

DOI

http://dx.doi.org/10.1007/bf00472631

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1029171943


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": "Scientific Research Institute for Physical and Organic Chemistry, M. A. Suslov State University, 344104, Rostov-on-Don", 
          "id": "http://www.grid.ac/institutes/None", 
          "name": [
            "Scientific Research Institute for Physical and Organic Chemistry, M. A. Suslov State University, 344104, Rostov-on-Don"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Sadekov", 
        "givenName": "I. D.", 
        "id": "sg:person.010755516305.74", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010755516305.74"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Scientific Research Institute for Physical and Organic Chemistry, M. A. Suslov State University, 344104, Rostov-on-Don", 
          "id": "http://www.grid.ac/institutes/None", 
          "name": [
            "Scientific Research Institute for Physical and Organic Chemistry, M. A. Suslov State University, 344104, Rostov-on-Don"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Abakarov", 
        "givenName": "G. M.", 
        "id": "sg:person.011750576150.12", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011750576150.12"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Scientific Research Institute for Physical and Organic Chemistry, M. A. Suslov State University, 344104, Rostov-on-Don", 
          "id": "http://www.grid.ac/institutes/None", 
          "name": [
            "Scientific Research Institute for Physical and Organic Chemistry, M. A. Suslov State University, 344104, Rostov-on-Don"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Shneider", 
        "givenName": "A. A.", 
        "id": "sg:person.07560763377.40", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07560763377.40"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Scientific Research Institute for Physical and Organic Chemistry, M. A. Suslov State University, 344104, Rostov-on-Don", 
          "id": "http://www.grid.ac/institutes/None", 
          "name": [
            "Scientific Research Institute for Physical and Organic Chemistry, M. A. Suslov State University, 344104, Rostov-on-Don"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Kuren'", 
        "givenName": "S. G.", 
        "id": "sg:person.011153724377.22", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011153724377.22"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Scientific Research Institute for Physical and Organic Chemistry, M. A. Suslov State University, 344104, Rostov-on-Don", 
          "id": "http://www.grid.ac/institutes/None", 
          "name": [
            "Scientific Research Institute for Physical and Organic Chemistry, M. A. Suslov State University, 344104, Rostov-on-Don"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Starikov", 
        "givenName": "A. G.", 
        "id": "sg:person.014454430517.25", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014454430517.25"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Scientific Research Institute for Physical and Organic Chemistry, M. A. Suslov State University, 344104, Rostov-on-Don", 
          "id": "http://www.grid.ac/institutes/None", 
          "name": [
            "Scientific Research Institute for Physical and Organic Chemistry, M. A. Suslov State University, 344104, Rostov-on-Don"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Garnovskii", 
        "givenName": "A. D.", 
        "id": "sg:person.014222624313.54", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014222624313.54"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Scientific Research Institute for Physical and Organic Chemistry, M. A. Suslov State University, 344104, Rostov-on-Don", 
          "id": "http://www.grid.ac/institutes/None", 
          "name": [
            "Scientific Research Institute for Physical and Organic Chemistry, M. A. Suslov State University, 344104, Rostov-on-Don"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Minkin", 
        "givenName": "V. I.", 
        "id": "sg:person.07535265367.87", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07535265367.87"
        ], 
        "type": "Person"
      }
    ], 
    "datePublished": "1989-01", 
    "datePublishedReg": "1989-01-01", 
    "description": "Several 2-substituted benzotellurazoles have been prepared by the reaction of N-allyl derivatives of o-methyltelluroaniline with POC13 or SOC12 followed by reduction of the \u03c3-telluranes which are formed. The use of the zinc and sodium salts of o-aminotellurophenol and 2-chlorotellurenylazobenzene, in a procedure similar to that used to prepare benzothiazoles and benzoselenazoles, did not lead to the formation of benzotellurazoles.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/bf00472631", 
    "inLanguage": "en", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1429545", 
        "issn": [
          "0132-6244", 
          "1573-8353"
        ], 
        "name": "Chemistry of Heterocyclic Compounds", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "1", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "25"
      }
    ], 
    "keywords": [
      "allyl derivatives", 
      "sodium salt", 
      "telluranes", 
      "benzoselenazoles", 
      "heterocycles", 
      "benzothiazole", 
      "salt", 
      "derivatives", 
      "reaction", 
      "POC13", 
      "SOC12", 
      "zinc", 
      "formation", 
      "reduction", 
      "procedure", 
      "use"
    ], 
    "name": "Nitrogen-tellurium heterocycles", 
    "pagination": "103-108", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1029171943"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/bf00472631"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/bf00472631", 
      "https://app.dimensions.ai/details/publication/pub.1029171943"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-05-20T07:18", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20220519/entities/gbq_results/article/article_201.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/bf00472631"
  }
]
 

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/bf00472631'

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/bf00472631'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf00472631'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf00472631'


 

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

116 TRIPLES      21 PREDICATES      42 URIs      34 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/bf00472631 schema:about anzsrc-for:03
2 anzsrc-for:0305
3 schema:author N26da3b24e5be4d90a7ecdc8b98900e5c
4 schema:datePublished 1989-01
5 schema:datePublishedReg 1989-01-01
6 schema:description Several 2-substituted benzotellurazoles have been prepared by the reaction of N-allyl derivatives of o-methyltelluroaniline with POC13 or SOC12 followed by reduction of the σ-telluranes which are formed. The use of the zinc and sodium salts of o-aminotellurophenol and 2-chlorotellurenylazobenzene, in a procedure similar to that used to prepare benzothiazoles and benzoselenazoles, did not lead to the formation of benzotellurazoles.
7 schema:genre article
8 schema:inLanguage en
9 schema:isAccessibleForFree false
10 schema:isPartOf N7adbce98a16241ca920ff117e6a2d107
11 Nc659da168eac4eafa849ae1b3d5c04ce
12 sg:journal.1429545
13 schema:keywords POC13
14 SOC12
15 allyl derivatives
16 benzoselenazoles
17 benzothiazole
18 derivatives
19 formation
20 heterocycles
21 procedure
22 reaction
23 reduction
24 salt
25 sodium salt
26 telluranes
27 use
28 zinc
29 schema:name Nitrogen-tellurium heterocycles
30 schema:pagination 103-108
31 schema:productId N9fb407458c7e499cafbde323930a7ea4
32 Nd69b0468954c43a1963c2541815a7bc7
33 schema:sameAs https://app.dimensions.ai/details/publication/pub.1029171943
34 https://doi.org/10.1007/bf00472631
35 schema:sdDatePublished 2022-05-20T07:18
36 schema:sdLicense https://scigraph.springernature.com/explorer/license/
37 schema:sdPublisher N4cec36859fe341408c6fa9afbf986606
38 schema:url https://doi.org/10.1007/bf00472631
39 sgo:license sg:explorer/license/
40 sgo:sdDataset articles
41 rdf:type schema:ScholarlyArticle
42 N26da3b24e5be4d90a7ecdc8b98900e5c rdf:first sg:person.010755516305.74
43 rdf:rest N78d828155c4142de86258f508f11d06a
44 N4cec36859fe341408c6fa9afbf986606 schema:name Springer Nature - SN SciGraph project
45 rdf:type schema:Organization
46 N4de503ff48224a66b253470c4a5de6d6 rdf:first sg:person.011153724377.22
47 rdf:rest N57a4f28dfbf54afb95361a7076f6e6c8
48 N53c538a11ec4451c903ae607b22ee865 rdf:first sg:person.014222624313.54
49 rdf:rest Na60f50b391b4439cb433c1d7d1e6d8b7
50 N57a4f28dfbf54afb95361a7076f6e6c8 rdf:first sg:person.014454430517.25
51 rdf:rest N53c538a11ec4451c903ae607b22ee865
52 N659bc85c67f7433c8a3492eb1d8e231c rdf:first sg:person.07560763377.40
53 rdf:rest N4de503ff48224a66b253470c4a5de6d6
54 N78d828155c4142de86258f508f11d06a rdf:first sg:person.011750576150.12
55 rdf:rest N659bc85c67f7433c8a3492eb1d8e231c
56 N7adbce98a16241ca920ff117e6a2d107 schema:issueNumber 1
57 rdf:type schema:PublicationIssue
58 N9fb407458c7e499cafbde323930a7ea4 schema:name dimensions_id
59 schema:value pub.1029171943
60 rdf:type schema:PropertyValue
61 Na60f50b391b4439cb433c1d7d1e6d8b7 rdf:first sg:person.07535265367.87
62 rdf:rest rdf:nil
63 Nc659da168eac4eafa849ae1b3d5c04ce schema:volumeNumber 25
64 rdf:type schema:PublicationVolume
65 Nd69b0468954c43a1963c2541815a7bc7 schema:name doi
66 schema:value 10.1007/bf00472631
67 rdf:type schema:PropertyValue
68 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
69 schema:name Chemical Sciences
70 rdf:type schema:DefinedTerm
71 anzsrc-for:0305 schema:inDefinedTermSet anzsrc-for:
72 schema:name Organic Chemistry
73 rdf:type schema:DefinedTerm
74 sg:journal.1429545 schema:issn 0132-6244
75 1573-8353
76 schema:name Chemistry of Heterocyclic Compounds
77 schema:publisher Springer Nature
78 rdf:type schema:Periodical
79 sg:person.010755516305.74 schema:affiliation grid-institutes:None
80 schema:familyName Sadekov
81 schema:givenName I. D.
82 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010755516305.74
83 rdf:type schema:Person
84 sg:person.011153724377.22 schema:affiliation grid-institutes:None
85 schema:familyName Kuren'
86 schema:givenName S. G.
87 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011153724377.22
88 rdf:type schema:Person
89 sg:person.011750576150.12 schema:affiliation grid-institutes:None
90 schema:familyName Abakarov
91 schema:givenName G. M.
92 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011750576150.12
93 rdf:type schema:Person
94 sg:person.014222624313.54 schema:affiliation grid-institutes:None
95 schema:familyName Garnovskii
96 schema:givenName A. D.
97 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014222624313.54
98 rdf:type schema:Person
99 sg:person.014454430517.25 schema:affiliation grid-institutes:None
100 schema:familyName Starikov
101 schema:givenName A. G.
102 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014454430517.25
103 rdf:type schema:Person
104 sg:person.07535265367.87 schema:affiliation grid-institutes:None
105 schema:familyName Minkin
106 schema:givenName V. I.
107 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07535265367.87
108 rdf:type schema:Person
109 sg:person.07560763377.40 schema:affiliation grid-institutes:None
110 schema:familyName Shneider
111 schema:givenName A. A.
112 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07560763377.40
113 rdf:type schema:Person
114 grid-institutes:None schema:alternateName Scientific Research Institute for Physical and Organic Chemistry, M. A. Suslov State University, 344104, Rostov-on-Don
115 schema:name Scientific Research Institute for Physical and Organic Chemistry, M. A. Suslov State University, 344104, Rostov-on-Don
116 rdf:type schema:Organization
 




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


...