Some derivatives of 5-eicosenoic acid View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1966-10

AUTHORS

Sara P. Fore, Gene Sumrell

ABSTRACT

cis-5-Eicosenoic acid and its methyl ester have been epoxidized. Preparation of an hydroxylactone through lactonizaton of both the 5,6-epoxy acid and the 5,6-dihydroxy acid has been investigated. 5-Eicosenoic acid has also been converted to γ-lactone through use of perchloric orp-toluenesulfonic acid. The preparation of several other related new compounds is described. More... »

PAGES

581-584

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf02641192

DOI

http://dx.doi.org/10.1007/bf02641192

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1017119067


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/2008/09", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Engineering", 
        "type": "DefinedTerm"
      }, 
      {
        "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/0904", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Chemical Engineering", 
        "type": "DefinedTerm"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "Southern Regional Research Laboratory, New Orlenas, Louisiana", 
          "id": "http://www.grid.ac/institutes/grid.507314.4", 
          "name": [
            "Southern Regional Research Laboratory, New Orlenas, Louisiana"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Fore", 
        "givenName": "Sara P.", 
        "id": "sg:person.07443054053.51", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07443054053.51"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Southern Regional Research Laboratory, New Orlenas, Louisiana", 
          "id": "http://www.grid.ac/institutes/grid.507314.4", 
          "name": [
            "Southern Regional Research Laboratory, New Orlenas, Louisiana"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Sumrell", 
        "givenName": "Gene", 
        "id": "sg:person.053045073.19", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.053045073.19"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "sg:pub.10.1007/bf02971182", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1018790519", 
          "https://doi.org/10.1007/bf02971182"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "1966-10", 
    "datePublishedReg": "1966-10-01", 
    "description": "Abstractcis-5-Eicosenoic acid and its methyl ester have been epoxidized. Preparation of an hydroxylactone through lactonizaton of both the 5,6-epoxy acid and the 5,6-dihydroxy acid has been investigated. 5-Eicosenoic acid has also been converted to \u03b3-lactone through use of perchloric orp-toluenesulfonic acid. The preparation of several other related new compounds is described.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/bf02641192", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1082739", 
        "issn": [
          "0003-021X", 
          "1558-9331"
        ], 
        "name": "Journal of the American Oil Chemists' Society", 
        "publisher": "Wiley", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "10", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "43"
      }
    ], 
    "keywords": [
      "related new compounds", 
      "new compounds", 
      "\u03b3-lactones", 
      "dihydroxy acids", 
      "epoxy acids", 
      "methyl ester", 
      "acid", 
      "preparation", 
      "compounds", 
      "derivatives", 
      "esters", 
      "hydroxylactones", 
      "use"
    ], 
    "name": "Some derivatives of 5-eicosenoic acid", 
    "pagination": "581-584", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1017119067"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/bf02641192"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/bf02641192", 
      "https://app.dimensions.ai/details/publication/pub.1017119067"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-08-04T17:12", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20220804/entities/gbq_results/article/article_99.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/bf02641192"
  }
]
 

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/bf02641192'

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/bf02641192'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf02641192'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf02641192'


 

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

81 TRIPLES      21 PREDICATES      39 URIs      30 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/bf02641192 schema:about anzsrc-for:09
2 anzsrc-for:0904
3 schema:author Nca83362a139b4e1f99fb3970e4a0c253
4 schema:citation sg:pub.10.1007/bf02971182
5 schema:datePublished 1966-10
6 schema:datePublishedReg 1966-10-01
7 schema:description Abstractcis-5-Eicosenoic acid and its methyl ester have been epoxidized. Preparation of an hydroxylactone through lactonizaton of both the 5,6-epoxy acid and the 5,6-dihydroxy acid has been investigated. 5-Eicosenoic acid has also been converted to γ-lactone through use of perchloric orp-toluenesulfonic acid. The preparation of several other related new compounds is described.
8 schema:genre article
9 schema:isAccessibleForFree false
10 schema:isPartOf N1a6e322e52734b199b88d127bb3e5089
11 N9ae3083b1c3c47fcbb76972573badf1d
12 sg:journal.1082739
13 schema:keywords acid
14 compounds
15 derivatives
16 dihydroxy acids
17 epoxy acids
18 esters
19 hydroxylactones
20 methyl ester
21 new compounds
22 preparation
23 related new compounds
24 use
25 γ-lactones
26 schema:name Some derivatives of 5-eicosenoic acid
27 schema:pagination 581-584
28 schema:productId Nca75e729fde44c3fa5eb9243e762bfbc
29 Ncece24c8dca542718d7dbd7cb1afa707
30 schema:sameAs https://app.dimensions.ai/details/publication/pub.1017119067
31 https://doi.org/10.1007/bf02641192
32 schema:sdDatePublished 2022-08-04T17:12
33 schema:sdLicense https://scigraph.springernature.com/explorer/license/
34 schema:sdPublisher Nad0464a8dfe04dcf90b11de6096c6b56
35 schema:url https://doi.org/10.1007/bf02641192
36 sgo:license sg:explorer/license/
37 sgo:sdDataset articles
38 rdf:type schema:ScholarlyArticle
39 N1a6e322e52734b199b88d127bb3e5089 schema:issueNumber 10
40 rdf:type schema:PublicationIssue
41 N9ae3083b1c3c47fcbb76972573badf1d schema:volumeNumber 43
42 rdf:type schema:PublicationVolume
43 Nad0464a8dfe04dcf90b11de6096c6b56 schema:name Springer Nature - SN SciGraph project
44 rdf:type schema:Organization
45 Nca75e729fde44c3fa5eb9243e762bfbc schema:name dimensions_id
46 schema:value pub.1017119067
47 rdf:type schema:PropertyValue
48 Nca83362a139b4e1f99fb3970e4a0c253 rdf:first sg:person.07443054053.51
49 rdf:rest Nea565fcdd97249e68f8618131dfe49f2
50 Ncece24c8dca542718d7dbd7cb1afa707 schema:name doi
51 schema:value 10.1007/bf02641192
52 rdf:type schema:PropertyValue
53 Nea565fcdd97249e68f8618131dfe49f2 rdf:first sg:person.053045073.19
54 rdf:rest rdf:nil
55 anzsrc-for:09 schema:inDefinedTermSet anzsrc-for:
56 schema:name Engineering
57 rdf:type schema:DefinedTerm
58 anzsrc-for:0904 schema:inDefinedTermSet anzsrc-for:
59 schema:name Chemical Engineering
60 rdf:type schema:DefinedTerm
61 sg:journal.1082739 schema:issn 0003-021X
62 1558-9331
63 schema:name Journal of the American Oil Chemists' Society
64 schema:publisher Wiley
65 rdf:type schema:Periodical
66 sg:person.053045073.19 schema:affiliation grid-institutes:grid.507314.4
67 schema:familyName Sumrell
68 schema:givenName Gene
69 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.053045073.19
70 rdf:type schema:Person
71 sg:person.07443054053.51 schema:affiliation grid-institutes:grid.507314.4
72 schema:familyName Fore
73 schema:givenName Sara P.
74 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07443054053.51
75 rdf:type schema:Person
76 sg:pub.10.1007/bf02971182 schema:sameAs https://app.dimensions.ai/details/publication/pub.1018790519
77 https://doi.org/10.1007/bf02971182
78 rdf:type schema:CreativeWork
79 grid-institutes:grid.507314.4 schema:alternateName Southern Regional Research Laboratory, New Orlenas, Louisiana
80 schema:name Southern Regional Research Laboratory, New Orlenas, Louisiana
81 rdf:type schema:Organization
 




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


...