Heterocyclizations of 1-(Benzothiazol-2-yl)-4-phenylthiosemicarbazide View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2008-03

AUTHORS

P. V. Savitskii, R. I. Vas’kevich, Yu. L. Zborovskii, V. I. Staninets, S. A. But, A. N. Chernega

ABSTRACT

1-(Benzothiazol-2-yl)-4-phenylthiosemicarbazide reacted with methyl iodide in the presence of sodium acetate in boiling ethanol to give 2,2′-dithiobis[N-(5-methylsulfanyl-4-phenyl-4H-1,2,4-triazol-3-yl)-benzenamine]. The reaction of the title compound with dimethyl acetylenedicarboxylate in dioxane led to the formation of methyl 3-(benzothiazol-2-yl)-2-(2-methoxy-2-oxoethyl)-2,3-dihydro-1,3,4-thiadiazole-2-carboxylate.

PAGES

402-406

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070428008030159

DOI

http://dx.doi.org/10.1134/s1070428008030159

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1033779113


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/2008/0601", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Biochemistry and Cell Biology", 
        "type": "DefinedTerm"
      }, 
      {
        "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/06", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Biological Sciences", 
        "type": "DefinedTerm"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "Institute of Organic Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.464621.3", 
          "name": [
            "Institute of Organic Chemistry, National Academy of Sciences of Ukraine, ul. Murmanskaya 5, 02660, Kiev, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Savitskii", 
        "givenName": "P. V.", 
        "id": "sg:person.015551724522.27", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015551724522.27"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Organic Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.464621.3", 
          "name": [
            "Institute of Organic Chemistry, National Academy of Sciences of Ukraine, ul. Murmanskaya 5, 02660, Kiev, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Vas\u2019kevich", 
        "givenName": "R. I.", 
        "id": "sg:person.013174754337.67", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013174754337.67"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Organic Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.464621.3", 
          "name": [
            "Institute of Organic Chemistry, National Academy of Sciences of Ukraine, ul. Murmanskaya 5, 02660, Kiev, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Zborovskii", 
        "givenName": "Yu. L.", 
        "id": "sg:person.010120771367.48", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010120771367.48"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Organic Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.464621.3", 
          "name": [
            "Institute of Organic Chemistry, National Academy of Sciences of Ukraine, ul. Murmanskaya 5, 02660, Kiev, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Staninets", 
        "givenName": "V. I.", 
        "id": "sg:person.016653667731.06", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016653667731.06"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Organic Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.464621.3", 
          "name": [
            "Institute of Organic Chemistry, National Academy of Sciences of Ukraine, ul. Murmanskaya 5, 02660, Kiev, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "But", 
        "givenName": "S. A.", 
        "id": "sg:person.010255165537.98", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010255165537.98"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Organic Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.464621.3", 
          "name": [
            "Institute of Organic Chemistry, National Academy of Sciences of Ukraine, ul. Murmanskaya 5, 02660, Kiev, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Chernega", 
        "givenName": "A. N.", 
        "id": "sg:person.013701677755.94", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013701677755.94"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "https://doi.org/10.1107/s0567740876009989", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1004032002"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1107/s0567739468000707", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1006361149"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1134/s1070428006090272", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1017125269", 
          "https://doi.org/10.1134/s1070428006090272"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1107/s0567739479001613", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1023477475"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1023/b:rujo.0000045202.20807.f8", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1045266273", 
          "https://doi.org/10.1023/b:rujo.0000045202.20807.f8"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1107/s0567740881005943", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1047682328"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1134/s1070428006090260", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1050379983", 
          "https://doi.org/10.1134/s1070428006090260"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2008-03", 
    "datePublishedReg": "2008-03-01", 
    "description": "1-(Benzothiazol-2-yl)-4-phenylthiosemicarbazide reacted with methyl iodide in the presence of sodium acetate in boiling ethanol to give 2,2\u2032-dithiobis[N-(5-methylsulfanyl-4-phenyl-4H-1,2,4-triazol-3-yl)-benzenamine]. The reaction of the title compound with dimethyl acetylenedicarboxylate in dioxane led to the formation of methyl 3-(benzothiazol-2-yl)-2-(2-methoxy-2-oxoethyl)-2,3-dihydro-1,3,4-thiadiazole-2-carboxylate.", 
    "genre": "research_article", 
    "id": "sg:pub.10.1134/s1070428008030159", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1136317", 
        "issn": [
          "1070-4280", 
          "1608-3393"
        ], 
        "name": "Russian Journal of Organic Chemistry", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "3", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "44"
      }
    ], 
    "name": "Heterocyclizations of 1-(Benzothiazol-2-yl)-4-phenylthiosemicarbazide", 
    "pagination": "402-406", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "a0e966a69b5f373abe8acbff809718a49c464af6b769a038c5c592d15445f2ee"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1134/s1070428008030159"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1033779113"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1134/s1070428008030159", 
      "https://app.dimensions.ai/details/publication/pub.1033779113"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-10T20:45", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-uberresearch-data-dimensions-target-20181106-alternative/cleanup/v134/2549eaecd7973599484d7c17b260dba0a4ecb94b/merge/v9/a6c9fde33151104705d4d7ff012ea9563521a3ce/jats-lookup/v90/0000000001_0000000264/records_8684_00000506.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "http://link.springer.com/10.1134%2FS1070428008030159"
  }
]
 

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/s1070428008030159'

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/s1070428008030159'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1134/s1070428008030159'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1134/s1070428008030159'


 

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

120 TRIPLES      21 PREDICATES      34 URIs      19 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1134/s1070428008030159 schema:about anzsrc-for:06
2 anzsrc-for:0601
3 schema:author N082d7d32b9c94ca9a554362b963a8078
4 schema:citation sg:pub.10.1023/b:rujo.0000045202.20807.f8
5 sg:pub.10.1134/s1070428006090260
6 sg:pub.10.1134/s1070428006090272
7 https://doi.org/10.1107/s0567739468000707
8 https://doi.org/10.1107/s0567739479001613
9 https://doi.org/10.1107/s0567740876009989
10 https://doi.org/10.1107/s0567740881005943
11 schema:datePublished 2008-03
12 schema:datePublishedReg 2008-03-01
13 schema:description 1-(Benzothiazol-2-yl)-4-phenylthiosemicarbazide reacted with methyl iodide in the presence of sodium acetate in boiling ethanol to give 2,2′-dithiobis[N-(5-methylsulfanyl-4-phenyl-4H-1,2,4-triazol-3-yl)-benzenamine]. The reaction of the title compound with dimethyl acetylenedicarboxylate in dioxane led to the formation of methyl 3-(benzothiazol-2-yl)-2-(2-methoxy-2-oxoethyl)-2,3-dihydro-1,3,4-thiadiazole-2-carboxylate.
14 schema:genre research_article
15 schema:inLanguage en
16 schema:isAccessibleForFree false
17 schema:isPartOf N00950e3a76b144aabc940c3d7e5103fe
18 N61ecc0e0abcf4a35862a29eb456e0c93
19 sg:journal.1136317
20 schema:name Heterocyclizations of 1-(Benzothiazol-2-yl)-4-phenylthiosemicarbazide
21 schema:pagination 402-406
22 schema:productId N2ee2112e401b4e88bad52ae89f1179fa
23 N6aff2533fff943b1a70f72048c3be1c4
24 Nee99838aad1e4a9bb989285ffc4525c8
25 schema:sameAs https://app.dimensions.ai/details/publication/pub.1033779113
26 https://doi.org/10.1134/s1070428008030159
27 schema:sdDatePublished 2019-04-10T20:45
28 schema:sdLicense https://scigraph.springernature.com/explorer/license/
29 schema:sdPublisher N13411308601542d7a1ec10aafdbc859d
30 schema:url http://link.springer.com/10.1134%2FS1070428008030159
31 sgo:license sg:explorer/license/
32 sgo:sdDataset articles
33 rdf:type schema:ScholarlyArticle
34 N00950e3a76b144aabc940c3d7e5103fe schema:issueNumber 3
35 rdf:type schema:PublicationIssue
36 N01a29ca69c384a3d8009cf60ecf54d11 rdf:first sg:person.010255165537.98
37 rdf:rest Nc601e7ba80934dc2892ab126fcb87598
38 N082d7d32b9c94ca9a554362b963a8078 rdf:first sg:person.015551724522.27
39 rdf:rest Ndf1a9af9cab04ff78276896c40f493a2
40 N13411308601542d7a1ec10aafdbc859d schema:name Springer Nature - SN SciGraph project
41 rdf:type schema:Organization
42 N2ee2112e401b4e88bad52ae89f1179fa schema:name dimensions_id
43 schema:value pub.1033779113
44 rdf:type schema:PropertyValue
45 N333442b102ee411eabc6a6580fe72cb8 rdf:first sg:person.016653667731.06
46 rdf:rest N01a29ca69c384a3d8009cf60ecf54d11
47 N61ecc0e0abcf4a35862a29eb456e0c93 schema:volumeNumber 44
48 rdf:type schema:PublicationVolume
49 N6aff2533fff943b1a70f72048c3be1c4 schema:name readcube_id
50 schema:value a0e966a69b5f373abe8acbff809718a49c464af6b769a038c5c592d15445f2ee
51 rdf:type schema:PropertyValue
52 N91e4a8b9d2314544af541cb04f18a7f1 rdf:first sg:person.010120771367.48
53 rdf:rest N333442b102ee411eabc6a6580fe72cb8
54 Nc601e7ba80934dc2892ab126fcb87598 rdf:first sg:person.013701677755.94
55 rdf:rest rdf:nil
56 Ndf1a9af9cab04ff78276896c40f493a2 rdf:first sg:person.013174754337.67
57 rdf:rest N91e4a8b9d2314544af541cb04f18a7f1
58 Nee99838aad1e4a9bb989285ffc4525c8 schema:name doi
59 schema:value 10.1134/s1070428008030159
60 rdf:type schema:PropertyValue
61 anzsrc-for:06 schema:inDefinedTermSet anzsrc-for:
62 schema:name Biological Sciences
63 rdf:type schema:DefinedTerm
64 anzsrc-for:0601 schema:inDefinedTermSet anzsrc-for:
65 schema:name Biochemistry and Cell Biology
66 rdf:type schema:DefinedTerm
67 sg:journal.1136317 schema:issn 1070-4280
68 1608-3393
69 schema:name Russian Journal of Organic Chemistry
70 rdf:type schema:Periodical
71 sg:person.010120771367.48 schema:affiliation https://www.grid.ac/institutes/grid.464621.3
72 schema:familyName Zborovskii
73 schema:givenName Yu. L.
74 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010120771367.48
75 rdf:type schema:Person
76 sg:person.010255165537.98 schema:affiliation https://www.grid.ac/institutes/grid.464621.3
77 schema:familyName But
78 schema:givenName S. A.
79 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010255165537.98
80 rdf:type schema:Person
81 sg:person.013174754337.67 schema:affiliation https://www.grid.ac/institutes/grid.464621.3
82 schema:familyName Vas’kevich
83 schema:givenName R. I.
84 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013174754337.67
85 rdf:type schema:Person
86 sg:person.013701677755.94 schema:affiliation https://www.grid.ac/institutes/grid.464621.3
87 schema:familyName Chernega
88 schema:givenName A. N.
89 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013701677755.94
90 rdf:type schema:Person
91 sg:person.015551724522.27 schema:affiliation https://www.grid.ac/institutes/grid.464621.3
92 schema:familyName Savitskii
93 schema:givenName P. V.
94 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015551724522.27
95 rdf:type schema:Person
96 sg:person.016653667731.06 schema:affiliation https://www.grid.ac/institutes/grid.464621.3
97 schema:familyName Staninets
98 schema:givenName V. I.
99 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016653667731.06
100 rdf:type schema:Person
101 sg:pub.10.1023/b:rujo.0000045202.20807.f8 schema:sameAs https://app.dimensions.ai/details/publication/pub.1045266273
102 https://doi.org/10.1023/b:rujo.0000045202.20807.f8
103 rdf:type schema:CreativeWork
104 sg:pub.10.1134/s1070428006090260 schema:sameAs https://app.dimensions.ai/details/publication/pub.1050379983
105 https://doi.org/10.1134/s1070428006090260
106 rdf:type schema:CreativeWork
107 sg:pub.10.1134/s1070428006090272 schema:sameAs https://app.dimensions.ai/details/publication/pub.1017125269
108 https://doi.org/10.1134/s1070428006090272
109 rdf:type schema:CreativeWork
110 https://doi.org/10.1107/s0567739468000707 schema:sameAs https://app.dimensions.ai/details/publication/pub.1006361149
111 rdf:type schema:CreativeWork
112 https://doi.org/10.1107/s0567739479001613 schema:sameAs https://app.dimensions.ai/details/publication/pub.1023477475
113 rdf:type schema:CreativeWork
114 https://doi.org/10.1107/s0567740876009989 schema:sameAs https://app.dimensions.ai/details/publication/pub.1004032002
115 rdf:type schema:CreativeWork
116 https://doi.org/10.1107/s0567740881005943 schema:sameAs https://app.dimensions.ai/details/publication/pub.1047682328
117 rdf:type schema:CreativeWork
118 https://www.grid.ac/institutes/grid.464621.3 schema:alternateName Institute of Organic Chemistry
119 schema:name Institute of Organic Chemistry, National Academy of Sciences of Ukraine, ul. Murmanskaya 5, 02660, Kiev, Ukraine
120 rdf:type schema:Organization
 




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


...