A new route for the synthesis of substituted 5-amino-4-cyanoimidazol-2-ones – precursors for the preparation of 3,6,7,9-tetrahydro-8H-purin-8-ones derivatives View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2011-06

AUTHORS

S. A. Chumachenko, O. V. Shablykin, A. P. Kozachenko, T. V. Osadchuk, V. S. Brovarets

ABSTRACT

5-Alkyl(aryl)amino-4-cyanoimidazol-2-ones were obtained on the basis of 2-alkoxycarbonylamino-3,3-dichloroacrylonitriles. They were then used for the synthesis of derivatives of 3,6,7,9-tetrahydro-8H-purin-8-ones.

PAGES

336

References to SciGraph publications

  • 2002-10. Furin at the cutting edge: From protein traffic to embryogenesis and disease in NATURE REVIEWS MOLECULAR CELL BIOLOGY
  • 2007-03. Nitration of 1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one derivatives in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1007/s10593-011-0762-8

    DOI

    http://dx.doi.org/10.1007/s10593-011-0762-8

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1010187537


    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", 
        "author": [
          {
            "affiliation": {
              "alternateName": "Institute of Bioorganic Chemistry and Petrochemistry", 
              "id": "https://www.grid.ac/institutes/grid.424920.9", 
              "name": [
                "Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 1 Murmanskaya St., 02660, Kyiv, Ukraine"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Chumachenko", 
            "givenName": "S. A.", 
            "id": "sg:person.01366561222.79", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01366561222.79"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Institute of Bioorganic Chemistry and Petrochemistry", 
              "id": "https://www.grid.ac/institutes/grid.424920.9", 
              "name": [
                "Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 1 Murmanskaya St., 02660, Kyiv, Ukraine"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Shablykin", 
            "givenName": "O. V.", 
            "id": "sg:person.01120365303.86", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01120365303.86"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Institute of Bioorganic Chemistry and Petrochemistry", 
              "id": "https://www.grid.ac/institutes/grid.424920.9", 
              "name": [
                "Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 1 Murmanskaya St., 02660, Kyiv, Ukraine"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Kozachenko", 
            "givenName": "A. P.", 
            "id": "sg:person.010162050171.14", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010162050171.14"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Institute of Bioorganic Chemistry and Petrochemistry", 
              "id": "https://www.grid.ac/institutes/grid.424920.9", 
              "name": [
                "Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 1 Murmanskaya St., 02660, Kyiv, Ukraine"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Osadchuk", 
            "givenName": "T. V.", 
            "id": "sg:person.01326277344.91", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01326277344.91"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Institute of Bioorganic Chemistry and Petrochemistry", 
              "id": "https://www.grid.ac/institutes/grid.424920.9", 
              "name": [
                "Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 1 Murmanskaya St., 02660, Kyiv, Ukraine"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Brovarets", 
            "givenName": "V. S.", 
            "id": "sg:person.010072133553.61", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010072133553.61"
            ], 
            "type": "Person"
          }
        ], 
        "citation": [
          {
            "id": "https://doi.org/10.1677/jme.0.0240001", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1005888313"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1042/bj3270625", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1008998395"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1042/bj3270625", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1008998395"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1016/s0960-894x(99)00108-0", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1010595501"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1016/s0040-4039(00)87300-1", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1014364058"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1248/cpb.51.608", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1018557265"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1038/nrm934", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1024352145", 
              "https://doi.org/10.1038/nrm934"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1038/nrm934", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1024352145", 
              "https://doi.org/10.1038/nrm934"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1248/cpb.45.75", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1029141075"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1248/cpb.38.2971", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1030833308"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1002/jhet.5570200537", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1046138549"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1070428007030153", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1053033950", 
              "https://doi.org/10.1134/s1070428007030153"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1021/jm00067a016", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1055934076"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1021/jm960132w", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1055957538"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1021/jm960132w", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1055957538"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://app.dimensions.ai/details/publication/pub.1076682862", 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://app.dimensions.ai/details/publication/pub.1077692368", 
            "type": "CreativeWork"
          }
        ], 
        "datePublished": "2011-06", 
        "datePublishedReg": "2011-06-01", 
        "description": "5-Alkyl(aryl)amino-4-cyanoimidazol-2-ones were obtained on the basis of 2-alkoxycarbonylamino-3,3-dichloroacrylonitriles. They were then used for the synthesis of derivatives of 3,6,7,9-tetrahydro-8H-purin-8-ones.", 
        "genre": "research_article", 
        "id": "sg:pub.10.1007/s10593-011-0762-8", 
        "inLanguage": [
          "en"
        ], 
        "isAccessibleForFree": false, 
        "isPartOf": [
          {
            "id": "sg:journal.1356886", 
            "issn": [
              "0009-3122", 
              "1573-8353"
            ], 
            "name": "Chemistry of Heterocyclic Compounds", 
            "type": "Periodical"
          }, 
          {
            "issueNumber": "3", 
            "type": "PublicationIssue"
          }, 
          {
            "type": "PublicationVolume", 
            "volumeNumber": "47"
          }
        ], 
        "name": "A new route for the synthesis of substituted 5-amino-4-cyanoimidazol-2-ones \u2013 precursors for the preparation of 3,6,7,9-tetrahydro-8H-purin-8-ones derivatives", 
        "pagination": "336", 
        "productId": [
          {
            "name": "readcube_id", 
            "type": "PropertyValue", 
            "value": [
              "3088ecf050d273742727ed3ba398885debdd18ea754cef7c67ee80915b154394"
            ]
          }, 
          {
            "name": "doi", 
            "type": "PropertyValue", 
            "value": [
              "10.1007/s10593-011-0762-8"
            ]
          }, 
          {
            "name": "dimensions_id", 
            "type": "PropertyValue", 
            "value": [
              "pub.1010187537"
            ]
          }
        ], 
        "sameAs": [
          "https://doi.org/10.1007/s10593-011-0762-8", 
          "https://app.dimensions.ai/details/publication/pub.1010187537"
        ], 
        "sdDataset": "articles", 
        "sdDatePublished": "2019-04-10T20:46", 
        "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/v90/0000000001_0000000264/records_8684_00000510.jsonl", 
        "type": "ScholarlyArticle", 
        "url": "http://link.springer.com/10.1007%2Fs10593-011-0762-8"
      }
    ]
     

    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/s10593-011-0762-8'

    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/s10593-011-0762-8'

    Turtle is a human-readable linked data format.

    curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s10593-011-0762-8'

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

    curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s10593-011-0762-8'


     

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

    123 TRIPLES      20 PREDICATES      39 URIs      19 LITERALS      7 BLANK NODES

    Subject Predicate Object
    1 sg:pub.10.1007/s10593-011-0762-8 schema:author N8f5868b7d1834f3b876abf0f43fca1cd
    2 schema:citation sg:pub.10.1038/nrm934
    3 sg:pub.10.1134/s1070428007030153
    4 https://app.dimensions.ai/details/publication/pub.1076682862
    5 https://app.dimensions.ai/details/publication/pub.1077692368
    6 https://doi.org/10.1002/jhet.5570200537
    7 https://doi.org/10.1016/s0040-4039(00)87300-1
    8 https://doi.org/10.1016/s0960-894x(99)00108-0
    9 https://doi.org/10.1021/jm00067a016
    10 https://doi.org/10.1021/jm960132w
    11 https://doi.org/10.1042/bj3270625
    12 https://doi.org/10.1248/cpb.38.2971
    13 https://doi.org/10.1248/cpb.45.75
    14 https://doi.org/10.1248/cpb.51.608
    15 https://doi.org/10.1677/jme.0.0240001
    16 schema:datePublished 2011-06
    17 schema:datePublishedReg 2011-06-01
    18 schema:description 5-Alkyl(aryl)amino-4-cyanoimidazol-2-ones were obtained on the basis of 2-alkoxycarbonylamino-3,3-dichloroacrylonitriles. They were then used for the synthesis of derivatives of 3,6,7,9-tetrahydro-8H-purin-8-ones.
    19 schema:genre research_article
    20 schema:inLanguage en
    21 schema:isAccessibleForFree false
    22 schema:isPartOf N257784d082e2434daac4f380bb701535
    23 N993b763a12c44553a634239d80a561d1
    24 sg:journal.1356886
    25 schema:name A new route for the synthesis of substituted 5-amino-4-cyanoimidazol-2-ones – precursors for the preparation of 3,6,7,9-tetrahydro-8H-purin-8-ones derivatives
    26 schema:pagination 336
    27 schema:productId N30cce58e9f64499ebb1f214ee20c1eef
    28 Ncbedd838cf4b42fb8c3aa665c597cdf8
    29 Nfbfc0eb18957437c948a5eb4f33d2024
    30 schema:sameAs https://app.dimensions.ai/details/publication/pub.1010187537
    31 https://doi.org/10.1007/s10593-011-0762-8
    32 schema:sdDatePublished 2019-04-10T20:46
    33 schema:sdLicense https://scigraph.springernature.com/explorer/license/
    34 schema:sdPublisher N33a262cc9dfc4cbab52cbf886282def9
    35 schema:url http://link.springer.com/10.1007%2Fs10593-011-0762-8
    36 sgo:license sg:explorer/license/
    37 sgo:sdDataset articles
    38 rdf:type schema:ScholarlyArticle
    39 N1b3df7e7d51c47c4aa31bbca308800c1 rdf:first sg:person.010072133553.61
    40 rdf:rest rdf:nil
    41 N257784d082e2434daac4f380bb701535 schema:volumeNumber 47
    42 rdf:type schema:PublicationVolume
    43 N2cd66f2a47af446b9ca3bea006df57b6 rdf:first sg:person.01120365303.86
    44 rdf:rest N907ad91831c94216ae39a6b59e912c12
    45 N30cce58e9f64499ebb1f214ee20c1eef schema:name doi
    46 schema:value 10.1007/s10593-011-0762-8
    47 rdf:type schema:PropertyValue
    48 N33a262cc9dfc4cbab52cbf886282def9 schema:name Springer Nature - SN SciGraph project
    49 rdf:type schema:Organization
    50 N53ca6e4a3d32411ead27e50eb519a41d rdf:first sg:person.01326277344.91
    51 rdf:rest N1b3df7e7d51c47c4aa31bbca308800c1
    52 N8f5868b7d1834f3b876abf0f43fca1cd rdf:first sg:person.01366561222.79
    53 rdf:rest N2cd66f2a47af446b9ca3bea006df57b6
    54 N907ad91831c94216ae39a6b59e912c12 rdf:first sg:person.010162050171.14
    55 rdf:rest N53ca6e4a3d32411ead27e50eb519a41d
    56 N993b763a12c44553a634239d80a561d1 schema:issueNumber 3
    57 rdf:type schema:PublicationIssue
    58 Ncbedd838cf4b42fb8c3aa665c597cdf8 schema:name readcube_id
    59 schema:value 3088ecf050d273742727ed3ba398885debdd18ea754cef7c67ee80915b154394
    60 rdf:type schema:PropertyValue
    61 Nfbfc0eb18957437c948a5eb4f33d2024 schema:name dimensions_id
    62 schema:value pub.1010187537
    63 rdf:type schema:PropertyValue
    64 sg:journal.1356886 schema:issn 0009-3122
    65 1573-8353
    66 schema:name Chemistry of Heterocyclic Compounds
    67 rdf:type schema:Periodical
    68 sg:person.010072133553.61 schema:affiliation https://www.grid.ac/institutes/grid.424920.9
    69 schema:familyName Brovarets
    70 schema:givenName V. S.
    71 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010072133553.61
    72 rdf:type schema:Person
    73 sg:person.010162050171.14 schema:affiliation https://www.grid.ac/institutes/grid.424920.9
    74 schema:familyName Kozachenko
    75 schema:givenName A. P.
    76 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010162050171.14
    77 rdf:type schema:Person
    78 sg:person.01120365303.86 schema:affiliation https://www.grid.ac/institutes/grid.424920.9
    79 schema:familyName Shablykin
    80 schema:givenName O. V.
    81 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01120365303.86
    82 rdf:type schema:Person
    83 sg:person.01326277344.91 schema:affiliation https://www.grid.ac/institutes/grid.424920.9
    84 schema:familyName Osadchuk
    85 schema:givenName T. V.
    86 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01326277344.91
    87 rdf:type schema:Person
    88 sg:person.01366561222.79 schema:affiliation https://www.grid.ac/institutes/grid.424920.9
    89 schema:familyName Chumachenko
    90 schema:givenName S. A.
    91 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01366561222.79
    92 rdf:type schema:Person
    93 sg:pub.10.1038/nrm934 schema:sameAs https://app.dimensions.ai/details/publication/pub.1024352145
    94 https://doi.org/10.1038/nrm934
    95 rdf:type schema:CreativeWork
    96 sg:pub.10.1134/s1070428007030153 schema:sameAs https://app.dimensions.ai/details/publication/pub.1053033950
    97 https://doi.org/10.1134/s1070428007030153
    98 rdf:type schema:CreativeWork
    99 https://app.dimensions.ai/details/publication/pub.1076682862 schema:CreativeWork
    100 https://app.dimensions.ai/details/publication/pub.1077692368 schema:CreativeWork
    101 https://doi.org/10.1002/jhet.5570200537 schema:sameAs https://app.dimensions.ai/details/publication/pub.1046138549
    102 rdf:type schema:CreativeWork
    103 https://doi.org/10.1016/s0040-4039(00)87300-1 schema:sameAs https://app.dimensions.ai/details/publication/pub.1014364058
    104 rdf:type schema:CreativeWork
    105 https://doi.org/10.1016/s0960-894x(99)00108-0 schema:sameAs https://app.dimensions.ai/details/publication/pub.1010595501
    106 rdf:type schema:CreativeWork
    107 https://doi.org/10.1021/jm00067a016 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055934076
    108 rdf:type schema:CreativeWork
    109 https://doi.org/10.1021/jm960132w schema:sameAs https://app.dimensions.ai/details/publication/pub.1055957538
    110 rdf:type schema:CreativeWork
    111 https://doi.org/10.1042/bj3270625 schema:sameAs https://app.dimensions.ai/details/publication/pub.1008998395
    112 rdf:type schema:CreativeWork
    113 https://doi.org/10.1248/cpb.38.2971 schema:sameAs https://app.dimensions.ai/details/publication/pub.1030833308
    114 rdf:type schema:CreativeWork
    115 https://doi.org/10.1248/cpb.45.75 schema:sameAs https://app.dimensions.ai/details/publication/pub.1029141075
    116 rdf:type schema:CreativeWork
    117 https://doi.org/10.1248/cpb.51.608 schema:sameAs https://app.dimensions.ai/details/publication/pub.1018557265
    118 rdf:type schema:CreativeWork
    119 https://doi.org/10.1677/jme.0.0240001 schema:sameAs https://app.dimensions.ai/details/publication/pub.1005888313
    120 rdf:type schema:CreativeWork
    121 https://www.grid.ac/institutes/grid.424920.9 schema:alternateName Institute of Bioorganic Chemistry and Petrochemistry
    122 schema:name Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 1 Murmanskaya St., 02660, Kyiv, Ukraine
    123 rdf:type schema:Organization
     




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


    ...