Synthesis of 1,3-thioxoketones from salicylaldehyde View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2013-04

AUTHORS

I. S. Semenova, V. N. Yarovenko, K. S. Levchenko, M. M. Krayushkin

ABSTRACT

A method for the synthesis of monothiodibenzoylmethanes was developed. The method involves a reaction of potassium thioacetate with 1-(2-hydroxyphenyl)-3-phenylpropynone prepared from salicylaldehyde.

PAGES

1022-1025

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-013-0135-9

DOI

http://dx.doi.org/10.1007/s11172-013-0135-9

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1016982706


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": "Semenova", 
        "givenName": "I. S.", 
        "id": "sg:person.010312476135.08", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010312476135.08"
        ], 
        "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": "Yarovenko", 
        "givenName": "V. N.", 
        "id": "sg:person.013442641550.93", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013442641550.93"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Central Research Technological Institute \u201cTekhnomash\u201d, 4 ul. Ivana Franko, 121108, Moscow, Russian Federation", 
          "id": "http://www.grid.ac/institutes/None", 
          "name": [
            "Central Research Technological Institute \u201cTekhnomash\u201d, 4 ul. Ivana Franko, 121108, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Levchenko", 
        "givenName": "K. S.", 
        "id": "sg:person.014302146365.38", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014302146365.38"
        ], 
        "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": "Krayushkin", 
        "givenName": "M. M.", 
        "id": "sg:person.07647613217.16", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07647613217.16"
        ], 
        "type": "Person"
      }
    ], 
    "datePublished": "2013-04", 
    "datePublishedReg": "2013-04-01", 
    "description": "A method for the synthesis of monothiodibenzoylmethanes was developed. The method involves a reaction of potassium thioacetate with 1-(2-hydroxyphenyl)-3-phenylpropynone prepared from salicylaldehyde.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/s11172-013-0135-9", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1022309", 
        "issn": [
          "1066-5285", 
          "1573-9171"
        ], 
        "name": "Russian Chemical Bulletin", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "4", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "62"
      }
    ], 
    "keywords": [
      "potassium thioacetate", 
      "salicylaldehyde", 
      "synthesis", 
      "monothiodibenzoylmethane", 
      "thioacetate", 
      "reaction", 
      "method"
    ], 
    "name": "Synthesis of 1,3-thioxoketones from salicylaldehyde", 
    "pagination": "1022-1025", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1016982706"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s11172-013-0135-9"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s11172-013-0135-9", 
      "https://app.dimensions.ai/details/publication/pub.1016982706"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-11-24T20:56", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20221124/entities/gbq_results/article/article_582.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/s11172-013-0135-9"
  }
]
 

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/s11172-013-0135-9'

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/s11172-013-0135-9'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s11172-013-0135-9'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s11172-013-0135-9'


 

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

84 TRIPLES      20 PREDICATES      31 URIs      24 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s11172-013-0135-9 schema:about anzsrc-for:03
2 schema:author N621f7ba0d4ff4ed1927313df7e53e15e
3 schema:datePublished 2013-04
4 schema:datePublishedReg 2013-04-01
5 schema:description A method for the synthesis of monothiodibenzoylmethanes was developed. The method involves a reaction of potassium thioacetate with 1-(2-hydroxyphenyl)-3-phenylpropynone prepared from salicylaldehyde.
6 schema:genre article
7 schema:isAccessibleForFree false
8 schema:isPartOf N6eb524c0426a45328150a17e490158a3
9 Nbe073c411ffe47b39974ee573cbc3cda
10 sg:journal.1022309
11 schema:keywords method
12 monothiodibenzoylmethane
13 potassium thioacetate
14 reaction
15 salicylaldehyde
16 synthesis
17 thioacetate
18 schema:name Synthesis of 1,3-thioxoketones from salicylaldehyde
19 schema:pagination 1022-1025
20 schema:productId N3227ca9e73504aeaa34aad773de9e71e
21 N38e8fdab4f0e4c4699fc1dfc51436a8f
22 schema:sameAs https://app.dimensions.ai/details/publication/pub.1016982706
23 https://doi.org/10.1007/s11172-013-0135-9
24 schema:sdDatePublished 2022-11-24T20:56
25 schema:sdLicense https://scigraph.springernature.com/explorer/license/
26 schema:sdPublisher Ne570d563a0e74c6695795a38426ad75c
27 schema:url https://doi.org/10.1007/s11172-013-0135-9
28 sgo:license sg:explorer/license/
29 sgo:sdDataset articles
30 rdf:type schema:ScholarlyArticle
31 N3227ca9e73504aeaa34aad773de9e71e schema:name dimensions_id
32 schema:value pub.1016982706
33 rdf:type schema:PropertyValue
34 N3502814a17a14fbfb82e4a0a26c28e26 rdf:first sg:person.07647613217.16
35 rdf:rest rdf:nil
36 N36ede29399824530ac1af094aa950535 rdf:first sg:person.014302146365.38
37 rdf:rest N3502814a17a14fbfb82e4a0a26c28e26
38 N38e8fdab4f0e4c4699fc1dfc51436a8f schema:name doi
39 schema:value 10.1007/s11172-013-0135-9
40 rdf:type schema:PropertyValue
41 N621f7ba0d4ff4ed1927313df7e53e15e rdf:first sg:person.010312476135.08
42 rdf:rest N8c41b3296b134dc4afa092672e2194a5
43 N6eb524c0426a45328150a17e490158a3 schema:volumeNumber 62
44 rdf:type schema:PublicationVolume
45 N8c41b3296b134dc4afa092672e2194a5 rdf:first sg:person.013442641550.93
46 rdf:rest N36ede29399824530ac1af094aa950535
47 Nbe073c411ffe47b39974ee573cbc3cda schema:issueNumber 4
48 rdf:type schema:PublicationIssue
49 Ne570d563a0e74c6695795a38426ad75c schema:name Springer Nature - SN SciGraph project
50 rdf:type schema:Organization
51 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
52 schema:name Chemical Sciences
53 rdf:type schema:DefinedTerm
54 sg:journal.1022309 schema:issn 1066-5285
55 1573-9171
56 schema:name Russian Chemical Bulletin
57 schema:publisher Springer Nature
58 rdf:type schema:Periodical
59 sg:person.010312476135.08 schema:affiliation grid-institutes:grid.439283.7
60 schema:familyName Semenova
61 schema:givenName I. S.
62 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010312476135.08
63 rdf:type schema:Person
64 sg:person.013442641550.93 schema:affiliation grid-institutes:grid.439283.7
65 schema:familyName Yarovenko
66 schema:givenName V. N.
67 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013442641550.93
68 rdf:type schema:Person
69 sg:person.014302146365.38 schema:affiliation grid-institutes:None
70 schema:familyName Levchenko
71 schema:givenName K. S.
72 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014302146365.38
73 rdf:type schema:Person
74 sg:person.07647613217.16 schema:affiliation grid-institutes:grid.439283.7
75 schema:familyName Krayushkin
76 schema:givenName M. M.
77 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07647613217.16
78 rdf:type schema:Person
79 grid-institutes:None schema:alternateName Central Research Technological Institute “Tekhnomash”, 4 ul. Ivana Franko, 121108, Moscow, Russian Federation
80 schema:name Central Research Technological Institute “Tekhnomash”, 4 ul. Ivana Franko, 121108, Moscow, Russian Federation
81 rdf:type schema:Organization
82 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
83 schema:name N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation
84 rdf:type schema:Organization
 




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


...