Synthesis of the amides and acid halides of 1,2,4-oxadiazole-3-carbohydroxamic acid View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1994-04

AUTHORS

V. G. Andrianov, V. G. Semenikhina, A. V. Eremeev

ABSTRACT

The reaction of diaminoglyoxime with carboxylic acid derivatives gave the amidoximes of 1,2,4-oxadiazole-3 carboxylic acid. It has been found that in the nitrozation of the obtained amidoximes in a solution of hydrochloric or hydrobromic acid the corresponding halooximes are formed.

PAGES

475-477

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf01169946

DOI

http://dx.doi.org/10.1007/bf01169946

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1028974442


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": [
      {
        "familyName": "Andrianov", 
        "givenName": "V. G.", 
        "id": "sg:person.016164060371.30", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016164060371.30"
        ], 
        "type": "Person"
      }, 
      {
        "familyName": "Semenikhina", 
        "givenName": "V. G.", 
        "id": "sg:person.07461007171.11", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07461007171.11"
        ], 
        "type": "Person"
      }, 
      {
        "familyName": "Eremeev", 
        "givenName": "A. V.", 
        "id": "sg:person.014471236413.16", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014471236413.16"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "sg:pub.10.1007/978-3-642-99991-8", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1019732887", 
          "https://doi.org/10.1007/978-3-642-99991-8"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "1994-04", 
    "datePublishedReg": "1994-04-01", 
    "description": "The reaction of diaminoglyoxime with carboxylic acid derivatives gave the amidoximes of 1,2,4-oxadiazole-3 carboxylic acid. It has been found that in the nitrozation of the obtained amidoximes in a solution of hydrochloric or hydrobromic acid the corresponding halooximes are formed.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/bf01169946", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1429545", 
        "issn": [
          "0132-6244", 
          "1573-8353"
        ], 
        "name": "Chemistry of Heterocyclic Compounds", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "4", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "30"
      }
    ], 
    "keywords": [
      "reaction of diaminoglyoxime", 
      "diaminoglyoxime", 
      "carboxylic acids", 
      "synthesis", 
      "acid", 
      "carboxylic acid derivatives", 
      "acid halides", 
      "hydrobromic acid", 
      "acid derivatives", 
      "solution", 
      "amidoximes", 
      "reaction", 
      "halides", 
      "amides", 
      "derivatives"
    ], 
    "name": "Synthesis of the amides and acid halides of 1,2,4-oxadiazole-3-carbohydroxamic acid", 
    "pagination": "475-477", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1028974442"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/bf01169946"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/bf01169946", 
      "https://app.dimensions.ai/details/publication/pub.1028974442"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-11-24T20:46", 
    "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_222.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/bf01169946"
  }
]
 

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/bf01169946'

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/bf01169946'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf01169946'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf01169946'


 

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

84 TRIPLES      21 PREDICATES      41 URIs      32 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/bf01169946 schema:about anzsrc-for:03
2 anzsrc-for:0305
3 schema:author N9bd81b0680fc4a2c83fe71d55261b69a
4 schema:citation sg:pub.10.1007/978-3-642-99991-8
5 schema:datePublished 1994-04
6 schema:datePublishedReg 1994-04-01
7 schema:description The reaction of diaminoglyoxime with carboxylic acid derivatives gave the amidoximes of 1,2,4-oxadiazole-3 carboxylic acid. It has been found that in the nitrozation of the obtained amidoximes in a solution of hydrochloric or hydrobromic acid the corresponding halooximes are formed.
8 schema:genre article
9 schema:isAccessibleForFree false
10 schema:isPartOf N03326478b3e84a028e513381ffcab2e2
11 N9b23919d8afc44a1a1f76224ddc0686d
12 sg:journal.1429545
13 schema:keywords acid
14 acid derivatives
15 acid halides
16 amides
17 amidoximes
18 carboxylic acid derivatives
19 carboxylic acids
20 derivatives
21 diaminoglyoxime
22 halides
23 hydrobromic acid
24 reaction
25 reaction of diaminoglyoxime
26 solution
27 synthesis
28 schema:name Synthesis of the amides and acid halides of 1,2,4-oxadiazole-3-carbohydroxamic acid
29 schema:pagination 475-477
30 schema:productId N0eed30fde5384185ae0af08cbf5d7a52
31 N25201a8efa134f1cb4e748f964f7165e
32 schema:sameAs https://app.dimensions.ai/details/publication/pub.1028974442
33 https://doi.org/10.1007/bf01169946
34 schema:sdDatePublished 2022-11-24T20:46
35 schema:sdLicense https://scigraph.springernature.com/explorer/license/
36 schema:sdPublisher N2b851cc3e32b4220a75152f0316107b6
37 schema:url https://doi.org/10.1007/bf01169946
38 sgo:license sg:explorer/license/
39 sgo:sdDataset articles
40 rdf:type schema:ScholarlyArticle
41 N03326478b3e84a028e513381ffcab2e2 schema:volumeNumber 30
42 rdf:type schema:PublicationVolume
43 N0eed30fde5384185ae0af08cbf5d7a52 schema:name doi
44 schema:value 10.1007/bf01169946
45 rdf:type schema:PropertyValue
46 N25201a8efa134f1cb4e748f964f7165e schema:name dimensions_id
47 schema:value pub.1028974442
48 rdf:type schema:PropertyValue
49 N2b851cc3e32b4220a75152f0316107b6 schema:name Springer Nature - SN SciGraph project
50 rdf:type schema:Organization
51 N674184af40d846618253114203f076ce rdf:first sg:person.014471236413.16
52 rdf:rest rdf:nil
53 N9b23919d8afc44a1a1f76224ddc0686d schema:issueNumber 4
54 rdf:type schema:PublicationIssue
55 N9bd81b0680fc4a2c83fe71d55261b69a rdf:first sg:person.016164060371.30
56 rdf:rest Nbf335e03644b4e14afda8be1b4f5c930
57 Nbf335e03644b4e14afda8be1b4f5c930 rdf:first sg:person.07461007171.11
58 rdf:rest N674184af40d846618253114203f076ce
59 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
60 schema:name Chemical Sciences
61 rdf:type schema:DefinedTerm
62 anzsrc-for:0305 schema:inDefinedTermSet anzsrc-for:
63 schema:name Organic Chemistry
64 rdf:type schema:DefinedTerm
65 sg:journal.1429545 schema:issn 0132-6244
66 1573-8353
67 schema:name Chemistry of Heterocyclic Compounds
68 schema:publisher Springer Nature
69 rdf:type schema:Periodical
70 sg:person.014471236413.16 schema:familyName Eremeev
71 schema:givenName A. V.
72 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014471236413.16
73 rdf:type schema:Person
74 sg:person.016164060371.30 schema:familyName Andrianov
75 schema:givenName V. G.
76 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016164060371.30
77 rdf:type schema:Person
78 sg:person.07461007171.11 schema:familyName Semenikhina
79 schema:givenName V. G.
80 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07461007171.11
81 rdf:type schema:Person
82 sg:pub.10.1007/978-3-642-99991-8 schema:sameAs https://app.dimensions.ai/details/publication/pub.1019732887
83 https://doi.org/10.1007/978-3-642-99991-8
84 rdf:type schema:CreativeWork
 




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


...