Phosphorylation of some new acenaphthenequinone derivatives View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2009-08

AUTHORS

E. A. El-Sawi, T. B. Mostafa, H. A. Radwan

ABSTRACT

Acenaphthenequinone reacted with diazofluorene, diphenyldiazomethane, phenybenzoyldiazomethane, phenacyl chloride, o-nitrobenzyl chloride, and diazohydroindenedione to give new oxadiazole, ketoepoxide and dioxadiazepine derivatives. They reacted with triphenylphosphine and triethylphosphite to give new organophosphorus compounds containing a six-membered or four-membered phosphorane ring. The structures were elucidated using IR, UV, NMR, and mass spectra, and elemental analyses. More... »

PAGES

981

References to SciGraph publications

  • 1932-03. Synthesen mit Diazomethan VII Weiteres über die Umsetzung von Aldehyden und Ketonen in MONATSHEFTE FÜR CHEMIE - CHEMICAL MONTHLY
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1007/s10593-009-0363-y

    DOI

    http://dx.doi.org/10.1007/s10593-009-0363-y

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1047349493


    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": "Ain Shams University", 
              "id": "https://www.grid.ac/institutes/grid.7269.a", 
              "name": [
                "Chemistry Department, Faculty of Girls for Arts, Science and Education, Ain Shams University, Heliopolis, Cairo, Egypt"
              ], 
              "type": "Organization"
            }, 
            "familyName": "El-Sawi", 
            "givenName": "E. A.", 
            "id": "sg:person.01031345015.93", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01031345015.93"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Ain Shams University", 
              "id": "https://www.grid.ac/institutes/grid.7269.a", 
              "name": [
                "Chemistry Department, Faculty of Girls for Arts, Science and Education, Ain Shams University, Heliopolis, Cairo, Egypt"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Mostafa", 
            "givenName": "T. B.", 
            "id": "sg:person.014677334331.40", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014677334331.40"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Ain Shams University", 
              "id": "https://www.grid.ac/institutes/grid.7269.a", 
              "name": [
                "Chemistry Department, Faculty of Girls for Arts, Science and Education, Ain Shams University, Heliopolis, Cairo, Egypt"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Radwan", 
            "givenName": "H. A.", 
            "id": "sg:person.014670350075.81", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014670350075.81"
            ], 
            "type": "Person"
          }
        ], 
        "citation": [
          {
            "id": "sg:pub.10.1007/bf01638230", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1026675657", 
              "https://doi.org/10.1007/bf01638230"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1039/jr9460000746", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1027897145"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1021/ja01082a009", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1055766757"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1021/jo01103a609", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1056004435"
            ], 
            "type": "CreativeWork"
          }
        ], 
        "datePublished": "2009-08", 
        "datePublishedReg": "2009-08-01", 
        "description": "Acenaphthenequinone reacted with diazofluorene, diphenyldiazomethane, phenybenzoyldiazomethane, phenacyl chloride, o-nitrobenzyl chloride, and diazohydroindenedione to give new oxadiazole, ketoepoxide and dioxadiazepine derivatives. They reacted with triphenylphosphine and triethylphosphite to give new organophosphorus compounds containing a six-membered or four-membered phosphorane ring. The structures were elucidated using IR, UV, NMR, and mass spectra, and elemental analyses.", 
        "genre": "non_research_article", 
        "id": "sg:pub.10.1007/s10593-009-0363-y", 
        "inLanguage": [
          "en"
        ], 
        "isAccessibleForFree": false, 
        "isPartOf": [
          {
            "id": "sg:journal.1356886", 
            "issn": [
              "0009-3122", 
              "1573-8353"
            ], 
            "name": "Chemistry of Heterocyclic Compounds", 
            "type": "Periodical"
          }, 
          {
            "issueNumber": "8", 
            "type": "PublicationIssue"
          }, 
          {
            "type": "PublicationVolume", 
            "volumeNumber": "45"
          }
        ], 
        "name": "Phosphorylation of some new acenaphthenequinone derivatives", 
        "pagination": "981", 
        "productId": [
          {
            "name": "readcube_id", 
            "type": "PropertyValue", 
            "value": [
              "e18eea4ec586a969739459a396b07e0fbb404473a308b8188140bd500f738c8e"
            ]
          }, 
          {
            "name": "doi", 
            "type": "PropertyValue", 
            "value": [
              "10.1007/s10593-009-0363-y"
            ]
          }, 
          {
            "name": "dimensions_id", 
            "type": "PropertyValue", 
            "value": [
              "pub.1047349493"
            ]
          }
        ], 
        "sameAs": [
          "https://doi.org/10.1007/s10593-009-0363-y", 
          "https://app.dimensions.ai/details/publication/pub.1047349493"
        ], 
        "sdDataset": "articles", 
        "sdDatePublished": "2019-04-11T14:30", 
        "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/v90/0000000373_0000000373/records_13090_00000001.jsonl", 
        "type": "ScholarlyArticle", 
        "url": "http://link.springer.com/10.1007%2Fs10593-009-0363-y"
      }
    ]
     

    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/s10593-009-0363-y'

    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/s10593-009-0363-y'

    Turtle is a human-readable linked data format.

    curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s10593-009-0363-y'

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

    curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s10593-009-0363-y'


     

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

    88 TRIPLES      21 PREDICATES      31 URIs      19 LITERALS      7 BLANK NODES

    Subject Predicate Object
    1 sg:pub.10.1007/s10593-009-0363-y schema:about anzsrc-for:06
    2 anzsrc-for:0601
    3 schema:author N2d94f8e74e1c48ad91b21bdcc291e75a
    4 schema:citation sg:pub.10.1007/bf01638230
    5 https://doi.org/10.1021/ja01082a009
    6 https://doi.org/10.1021/jo01103a609
    7 https://doi.org/10.1039/jr9460000746
    8 schema:datePublished 2009-08
    9 schema:datePublishedReg 2009-08-01
    10 schema:description Acenaphthenequinone reacted with diazofluorene, diphenyldiazomethane, phenybenzoyldiazomethane, phenacyl chloride, o-nitrobenzyl chloride, and diazohydroindenedione to give new oxadiazole, ketoepoxide and dioxadiazepine derivatives. They reacted with triphenylphosphine and triethylphosphite to give new organophosphorus compounds containing a six-membered or four-membered phosphorane ring. The structures were elucidated using IR, UV, NMR, and mass spectra, and elemental analyses.
    11 schema:genre non_research_article
    12 schema:inLanguage en
    13 schema:isAccessibleForFree false
    14 schema:isPartOf N8195578d47014ae18fe9aa78195cf41f
    15 Ne9cc21504794424681d9570633b6f3de
    16 sg:journal.1356886
    17 schema:name Phosphorylation of some new acenaphthenequinone derivatives
    18 schema:pagination 981
    19 schema:productId N4d5effa2e94a40d6a0707195171ecf10
    20 N711efa7af2d94ad2b688dfde790059ff
    21 Nc04e1a6faf764b83a4f1a85ee093699b
    22 schema:sameAs https://app.dimensions.ai/details/publication/pub.1047349493
    23 https://doi.org/10.1007/s10593-009-0363-y
    24 schema:sdDatePublished 2019-04-11T14:30
    25 schema:sdLicense https://scigraph.springernature.com/explorer/license/
    26 schema:sdPublisher Nbaead50ac85f46e4a5c856e459019b1e
    27 schema:url http://link.springer.com/10.1007%2Fs10593-009-0363-y
    28 sgo:license sg:explorer/license/
    29 sgo:sdDataset articles
    30 rdf:type schema:ScholarlyArticle
    31 N207c7013fe234d399987be35f55bcd1a rdf:first sg:person.014670350075.81
    32 rdf:rest rdf:nil
    33 N2d94f8e74e1c48ad91b21bdcc291e75a rdf:first sg:person.01031345015.93
    34 rdf:rest N42e7229c7d314ca99a8f4b5bd5f05776
    35 N42e7229c7d314ca99a8f4b5bd5f05776 rdf:first sg:person.014677334331.40
    36 rdf:rest N207c7013fe234d399987be35f55bcd1a
    37 N4d5effa2e94a40d6a0707195171ecf10 schema:name readcube_id
    38 schema:value e18eea4ec586a969739459a396b07e0fbb404473a308b8188140bd500f738c8e
    39 rdf:type schema:PropertyValue
    40 N711efa7af2d94ad2b688dfde790059ff schema:name doi
    41 schema:value 10.1007/s10593-009-0363-y
    42 rdf:type schema:PropertyValue
    43 N8195578d47014ae18fe9aa78195cf41f schema:volumeNumber 45
    44 rdf:type schema:PublicationVolume
    45 Nbaead50ac85f46e4a5c856e459019b1e schema:name Springer Nature - SN SciGraph project
    46 rdf:type schema:Organization
    47 Nc04e1a6faf764b83a4f1a85ee093699b schema:name dimensions_id
    48 schema:value pub.1047349493
    49 rdf:type schema:PropertyValue
    50 Ne9cc21504794424681d9570633b6f3de schema:issueNumber 8
    51 rdf:type schema:PublicationIssue
    52 anzsrc-for:06 schema:inDefinedTermSet anzsrc-for:
    53 schema:name Biological Sciences
    54 rdf:type schema:DefinedTerm
    55 anzsrc-for:0601 schema:inDefinedTermSet anzsrc-for:
    56 schema:name Biochemistry and Cell Biology
    57 rdf:type schema:DefinedTerm
    58 sg:journal.1356886 schema:issn 0009-3122
    59 1573-8353
    60 schema:name Chemistry of Heterocyclic Compounds
    61 rdf:type schema:Periodical
    62 sg:person.01031345015.93 schema:affiliation https://www.grid.ac/institutes/grid.7269.a
    63 schema:familyName El-Sawi
    64 schema:givenName E. A.
    65 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01031345015.93
    66 rdf:type schema:Person
    67 sg:person.014670350075.81 schema:affiliation https://www.grid.ac/institutes/grid.7269.a
    68 schema:familyName Radwan
    69 schema:givenName H. A.
    70 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014670350075.81
    71 rdf:type schema:Person
    72 sg:person.014677334331.40 schema:affiliation https://www.grid.ac/institutes/grid.7269.a
    73 schema:familyName Mostafa
    74 schema:givenName T. B.
    75 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014677334331.40
    76 rdf:type schema:Person
    77 sg:pub.10.1007/bf01638230 schema:sameAs https://app.dimensions.ai/details/publication/pub.1026675657
    78 https://doi.org/10.1007/bf01638230
    79 rdf:type schema:CreativeWork
    80 https://doi.org/10.1021/ja01082a009 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055766757
    81 rdf:type schema:CreativeWork
    82 https://doi.org/10.1021/jo01103a609 schema:sameAs https://app.dimensions.ai/details/publication/pub.1056004435
    83 rdf:type schema:CreativeWork
    84 https://doi.org/10.1039/jr9460000746 schema:sameAs https://app.dimensions.ai/details/publication/pub.1027897145
    85 rdf:type schema:CreativeWork
    86 https://www.grid.ac/institutes/grid.7269.a schema:alternateName Ain Shams University
    87 schema:name Chemistry Department, Faculty of Girls for Arts, Science and Education, Ain Shams University, Heliopolis, Cairo, Egypt
    88 rdf:type schema:Organization
     




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


    ...