Oxiranyl β-aminovinyl ketones. 5. Transformation of 2-methyl-2-(1-halogenoalkyl)-3(2h)-furanones into oxiranyl β-aminovinyl ketones View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1995-05

AUTHORS

D. Z. Stasevich, O. N. Bubel', M. V. Kudrevatykh, Ya. Musa

ABSTRACT

In reaction with amines 2-methyl-2-(1-halogenoalkyl)-3(2H) furanones form S-amino-1-halogeno-3-hydroxy-2-methyl-4 penten-3-ones and 6-amino-2-halogeno-3-hydroxy-3-methyl-5-hexen-3-ones, which are converted by the action of bases into the corresponding oxiranyl β-aminovinyl ketones.

PAGES

534-537

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf01166324

DOI

http://dx.doi.org/10.1007/bf01166324

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1025039984


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": "Stasevich", 
        "givenName": "D. Z.", 
        "type": "Person"
      }, 
      {
        "familyName": "Bubel'", 
        "givenName": "O. N.", 
        "id": "sg:person.012765005437.97", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012765005437.97"
        ], 
        "type": "Person"
      }, 
      {
        "familyName": "Kudrevatykh", 
        "givenName": "M. V.", 
        "id": "sg:person.011776572445.05", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011776572445.05"
        ], 
        "type": "Person"
      }, 
      {
        "familyName": "Musa", 
        "givenName": "Ya.", 
        "id": "sg:person.07746121752.33", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07746121752.33"
        ], 
        "type": "Person"
      }
    ], 
    "datePublished": "1995-05", 
    "datePublishedReg": "1995-05-01", 
    "description": "In reaction with amines 2-methyl-2-(1-halogenoalkyl)-3(2H) furanones form S-amino-1-halogeno-3-hydroxy-2-methyl-4 penten-3-ones and 6-amino-2-halogeno-3-hydroxy-3-methyl-5-hexen-3-ones, which are converted by the action of bases into the corresponding oxiranyl \u03b2-aminovinyl ketones.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/bf01166324", 
    "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": "5", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "31"
      }
    ], 
    "keywords": [
      "action", 
      "reaction", 
      "basis", 
      "amines", 
      "furanone", 
      "ketones", 
      "form S", 
      "transformation", 
      "aminovinyl ketones", 
      "action of bases"
    ], 
    "name": "Oxiranyl \u03b2-aminovinyl ketones. 5. Transformation of 2-methyl-2-(1-halogenoalkyl)-3(2h)-furanones into oxiranyl \u03b2-aminovinyl ketones", 
    "pagination": "534-537", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1025039984"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/bf01166324"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/bf01166324", 
      "https://app.dimensions.ai/details/publication/pub.1025039984"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-06-01T22:01", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20220601/entities/gbq_results/article/article_263.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/bf01166324"
  }
]
 

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/bf01166324'

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/bf01166324'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf01166324'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf01166324'


 

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

81 TRIPLES      21 PREDICATES      36 URIs      28 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/bf01166324 schema:about anzsrc-for:03
2 anzsrc-for:0305
3 schema:author N9e30b281bfe24e3cbaa0e240a076836f
4 schema:datePublished 1995-05
5 schema:datePublishedReg 1995-05-01
6 schema:description In reaction with amines 2-methyl-2-(1-halogenoalkyl)-3(2H) furanones form S-amino-1-halogeno-3-hydroxy-2-methyl-4 penten-3-ones and 6-amino-2-halogeno-3-hydroxy-3-methyl-5-hexen-3-ones, which are converted by the action of bases into the corresponding oxiranyl β-aminovinyl ketones.
7 schema:genre article
8 schema:inLanguage en
9 schema:isAccessibleForFree false
10 schema:isPartOf N0f79917241d54fd89eee781dea164ae0
11 N524423e393ee4b368e86bd54161d069e
12 sg:journal.1429545
13 schema:keywords action
14 action of bases
15 amines
16 aminovinyl ketones
17 basis
18 form S
19 furanone
20 ketones
21 reaction
22 transformation
23 schema:name Oxiranyl β-aminovinyl ketones. 5. Transformation of 2-methyl-2-(1-halogenoalkyl)-3(2h)-furanones into oxiranyl β-aminovinyl ketones
24 schema:pagination 534-537
25 schema:productId N5bd2d42e4c17434db0f3d74a806fa7e8
26 Nacadb960714b4c8185eebeb99de0b402
27 schema:sameAs https://app.dimensions.ai/details/publication/pub.1025039984
28 https://doi.org/10.1007/bf01166324
29 schema:sdDatePublished 2022-06-01T22:01
30 schema:sdLicense https://scigraph.springernature.com/explorer/license/
31 schema:sdPublisher N52c5ec2106c34b438a61419bd9526d1b
32 schema:url https://doi.org/10.1007/bf01166324
33 sgo:license sg:explorer/license/
34 sgo:sdDataset articles
35 rdf:type schema:ScholarlyArticle
36 N0f79917241d54fd89eee781dea164ae0 schema:volumeNumber 31
37 rdf:type schema:PublicationVolume
38 N524423e393ee4b368e86bd54161d069e schema:issueNumber 5
39 rdf:type schema:PublicationIssue
40 N52c5ec2106c34b438a61419bd9526d1b schema:name Springer Nature - SN SciGraph project
41 rdf:type schema:Organization
42 N5bd2d42e4c17434db0f3d74a806fa7e8 schema:name dimensions_id
43 schema:value pub.1025039984
44 rdf:type schema:PropertyValue
45 N9e30b281bfe24e3cbaa0e240a076836f rdf:first Nbe93e368f94549caaeae482d6f2ce4b5
46 rdf:rest Nffddde5385814a1d8830eecbcc1f5655
47 Nacadb960714b4c8185eebeb99de0b402 schema:name doi
48 schema:value 10.1007/bf01166324
49 rdf:type schema:PropertyValue
50 Nbe93e368f94549caaeae482d6f2ce4b5 schema:familyName Stasevich
51 schema:givenName D. Z.
52 rdf:type schema:Person
53 Nc01ae68297bf42aa92bde4cdee42d8f0 rdf:first sg:person.07746121752.33
54 rdf:rest rdf:nil
55 Ne9dbde0659304dad93c05daf6fa66f95 rdf:first sg:person.011776572445.05
56 rdf:rest Nc01ae68297bf42aa92bde4cdee42d8f0
57 Nffddde5385814a1d8830eecbcc1f5655 rdf:first sg:person.012765005437.97
58 rdf:rest Ne9dbde0659304dad93c05daf6fa66f95
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.011776572445.05 schema:familyName Kudrevatykh
71 schema:givenName M. V.
72 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011776572445.05
73 rdf:type schema:Person
74 sg:person.012765005437.97 schema:familyName Bubel'
75 schema:givenName O. N.
76 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012765005437.97
77 rdf:type schema:Person
78 sg:person.07746121752.33 schema:familyName Musa
79 schema:givenName Ya.
80 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07746121752.33
81 rdf:type schema:Person
 




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


...