Quantum chemical studies of pyrimidin-4-ones 3. 2-Oxo(thioxo, selenoxo)pyrimidin-4-ones and 5,6-dimethyl-2-oxo(thioxo)thieno[2,3-d]pyrimidin-4-ones View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2014-02

AUTHORS

M. Kh. Mamarakhmonov, L. I. Belen’kii, N. D. Chuvylkin, M. A. Ashirmatov, Kh. M. Shakhidoyatov

ABSTRACT

Quantum chemical calculations for 2-oxo-, 2-thioxo-, and 2-selenoxopyrimidin-4-ones, as well as for 5,6-dimethyl-2-oxo- and 5,6-dimethyl-2-thioxothieno[2,3-d]pyrimidin-4-ones, were carried out at the HF and DFT levels. An analysis of the relative energies shows that the 2-oxo form or the related thioxo or selenoxo forms are energetically more favorable in tautomeric interconversions of all the compounds under study both in the gas phase and in solutions in ethanol, acetonitrile, and DMSO. More... »

PAGES

350-354

References to SciGraph publications

  • 2011-02. Thieno[2,3-d]pyrimidin-4-ones 1. Condensation of 2,3-dimethyl- and 2,3-tri-, 2,3-tetra-, and 2,3-pentamethylene-7,8-dihydro-pyrrolo[1,2-a]thieno[2,3-d]pyriminidin-4(6H)-ones with aromatic aldehydes and furfural in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2001-02. Quantum-chemical estimates of geometric parameters of free radicals in RUSSIAN CHEMICAL BULLETIN
  • 2003-10. Quantum-chemical Studies of Pyrimidin-4-ones. 2. Stability in the Gas Phase of Tautomers of Pyrimidin-2,4-dione, 2-Thioxo-, 2-Selenoxo-, 2-Amino-, and 2-Acetylaminopyrimidin-4-ones, and Their 6-Methyl- and 6-Phenyl Derivatives in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2001-11. Electrophilic aromatic trichloromethylation: intermediates and products in RUSSIAN CHEMICAL BULLETIN
  • 1996-11. Relationships and features of electrophilic substitution reactions in the azole series in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2007-08. The sulfonation of pyrrole: Choice of relevant computational procedure for quantum chemical analysis of positional orientation in RUSSIAN CHEMICAL BULLETIN
  • 2011-11. Electronic structure and reactivity of 3-acetyl-2-methylbenzo[b]thiophene: a quantum chemical study in RUSSIAN CHEMICAL BULLETIN
  • 2005-04. Substrate and positional selectivity in electrophilic substitution reactions in pyrrole, furan, thiophene, and selenophene derivatives and related benzoannelated systems in RUSSIAN CHEMICAL BULLETIN
  • 2001-08. Quantum-chemical Investigations of Pyrimidinones-4. 1. Tautomerism of 2-Oxopyrimidinones-4 in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1007/s11172-014-0436-7

    DOI

    http://dx.doi.org/10.1007/s11172-014-0436-7

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1038761433


    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/2008/0306", 
            "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
            "name": "Physical Chemistry (incl. Structural)", 
            "type": "DefinedTerm"
          }, 
          {
            "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"
          }
        ], 
        "author": [
          {
            "affiliation": {
              "alternateName": "Academy of Sciences Republic of Uzbekistan", 
              "id": "https://www.grid.ac/institutes/grid.419209.7", 
              "name": [
                "Academician S. Yu. Yunusov Institute of Chemistry of Plant Substances, Academy of Sciences Republic of Uzbekistan, 77 ul. Mirzo Ulu gbeka, 100170, Tashkent, Uzbekistan"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Mamarakhmonov", 
            "givenName": "M. Kh.", 
            "id": "sg:person.016151244107.99", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016151244107.99"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Russian Academy of Sciences", 
              "id": "https://www.grid.ac/institutes/grid.4886.2", 
              "name": [
                "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Belen\u2019kii", 
            "givenName": "L. I.", 
            "id": "sg:person.016614773551.45", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016614773551.45"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Russian Academy of Sciences", 
              "id": "https://www.grid.ac/institutes/grid.4886.2", 
              "name": [
                "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Chuvylkin", 
            "givenName": "N. D.", 
            "id": "sg:person.010473055641.48", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010473055641.48"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Academy of Sciences Republic of Uzbekistan", 
              "id": "https://www.grid.ac/institutes/grid.419209.7", 
              "name": [
                "Academician S. Yu. Yunusov Institute of Chemistry of Plant Substances, Academy of Sciences Republic of Uzbekistan, 77 ul. Mirzo Ulu gbeka, 100170, Tashkent, Uzbekistan"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Ashirmatov", 
            "givenName": "M. A.", 
            "id": "sg:person.016557000703.78", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016557000703.78"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Academy of Sciences Republic of Uzbekistan", 
              "id": "https://www.grid.ac/institutes/grid.419209.7", 
              "name": [
                "Academician S. Yu. Yunusov Institute of Chemistry of Plant Substances, Academy of Sciences Republic of Uzbekistan, 77 ul. Mirzo Ulu gbeka, 100170, Tashkent, Uzbekistan"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Shakhidoyatov", 
            "givenName": "Kh. M.", 
            "id": "sg:person.015706066705.62", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015706066705.62"
            ], 
            "type": "Person"
          }
        ], 
        "citation": [
          {
            "id": "sg:pub.10.1023/a:1009501611921", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1001556840", 
              "https://doi.org/10.1023/a:1009501611921"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/s11172-011-0354-x", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1004877063", 
              "https://doi.org/10.1007/s11172-011-0354-x"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1023/a:1015024612380", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1005577299", 
              "https://doi.org/10.1023/a:1015024612380"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf01169964", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1011484408", 
              "https://doi.org/10.1007/bf01169964"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf01169964", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1011484408", 
              "https://doi.org/10.1007/bf01169964"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1002/jhet.5570330414", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1015537708"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1002/jhet.5570330414", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1015537708"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1023/b:cohc.0000010649.76065.65", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1015988714", 
              "https://doi.org/10.1023/b:cohc.0000010649.76065.65"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/s10593-011-0677-4", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1019113361", 
              "https://doi.org/10.1007/s10593-011-0677-4"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/s11172-007-0229-3", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1026005341", 
              "https://doi.org/10.1007/s11172-007-0229-3"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/s11172-005-0332-2", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1040773254", 
              "https://doi.org/10.1007/s11172-005-0332-2"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/s11172-005-0332-2", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1040773254", 
              "https://doi.org/10.1007/s11172-005-0332-2"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/s11172-005-0332-2", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1040773254", 
              "https://doi.org/10.1007/s11172-005-0332-2"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1023/a:1012791718619", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1052660853", 
              "https://doi.org/10.1023/a:1012791718619"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.1021/jo00120a012", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1055967902"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "https://doi.org/10.9734/acsj/2013/2966", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1074126468"
            ], 
            "type": "CreativeWork"
          }
        ], 
        "datePublished": "2014-02", 
        "datePublishedReg": "2014-02-01", 
        "description": "Quantum chemical calculations for 2-oxo-, 2-thioxo-, and 2-selenoxopyrimidin-4-ones, as well as for 5,6-dimethyl-2-oxo- and 5,6-dimethyl-2-thioxothieno[2,3-d]pyrimidin-4-ones, were carried out at the HF and DFT levels. An analysis of the relative energies shows that the 2-oxo form or the related thioxo or selenoxo forms are energetically more favorable in tautomeric interconversions of all the compounds under study both in the gas phase and in solutions in ethanol, acetonitrile, and DMSO.", 
        "genre": "research_article", 
        "id": "sg:pub.10.1007/s11172-014-0436-7", 
        "inLanguage": [
          "en"
        ], 
        "isAccessibleForFree": false, 
        "isPartOf": [
          {
            "id": "sg:journal.1022309", 
            "issn": [
              "1066-5285", 
              "1573-9171"
            ], 
            "name": "Russian Chemical Bulletin", 
            "type": "Periodical"
          }, 
          {
            "issueNumber": "2", 
            "type": "PublicationIssue"
          }, 
          {
            "type": "PublicationVolume", 
            "volumeNumber": "63"
          }
        ], 
        "name": "Quantum chemical studies of pyrimidin-4-ones 3. 2-Oxo(thioxo, selenoxo)pyrimidin-4-ones and 5,6-dimethyl-2-oxo(thioxo)thieno[2,3-d]pyrimidin-4-ones", 
        "pagination": "350-354", 
        "productId": [
          {
            "name": "readcube_id", 
            "type": "PropertyValue", 
            "value": [
              "b8a48b01d40e53fc49c6cf7bc5532bc93c680f4d77b6869f9bbd09b29247b96c"
            ]
          }, 
          {
            "name": "doi", 
            "type": "PropertyValue", 
            "value": [
              "10.1007/s11172-014-0436-7"
            ]
          }, 
          {
            "name": "dimensions_id", 
            "type": "PropertyValue", 
            "value": [
              "pub.1038761433"
            ]
          }
        ], 
        "sameAs": [
          "https://doi.org/10.1007/s11172-014-0436-7", 
          "https://app.dimensions.ai/details/publication/pub.1038761433"
        ], 
        "sdDataset": "articles", 
        "sdDatePublished": "2019-04-10T13:22", 
        "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_8659_00000533.jsonl", 
        "type": "ScholarlyArticle", 
        "url": "http://link.springer.com/10.1007%2Fs11172-014-0436-7"
      }
    ]
     

    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/s11172-014-0436-7'

    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/s11172-014-0436-7'

    Turtle is a human-readable linked data format.

    curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s11172-014-0436-7'

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

    curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s11172-014-0436-7'


     

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

    137 TRIPLES      21 PREDICATES      39 URIs      19 LITERALS      7 BLANK NODES

    Subject Predicate Object
    1 sg:pub.10.1007/s11172-014-0436-7 schema:about anzsrc-for:03
    2 anzsrc-for:0306
    3 schema:author N9da42e3fd26d4f109489614d4c06d244
    4 schema:citation sg:pub.10.1007/bf01169964
    5 sg:pub.10.1007/s10593-011-0677-4
    6 sg:pub.10.1007/s11172-005-0332-2
    7 sg:pub.10.1007/s11172-007-0229-3
    8 sg:pub.10.1007/s11172-011-0354-x
    9 sg:pub.10.1023/a:1009501611921
    10 sg:pub.10.1023/a:1012791718619
    11 sg:pub.10.1023/a:1015024612380
    12 sg:pub.10.1023/b:cohc.0000010649.76065.65
    13 https://doi.org/10.1002/jhet.5570330414
    14 https://doi.org/10.1021/jo00120a012
    15 https://doi.org/10.9734/acsj/2013/2966
    16 schema:datePublished 2014-02
    17 schema:datePublishedReg 2014-02-01
    18 schema:description Quantum chemical calculations for 2-oxo-, 2-thioxo-, and 2-selenoxopyrimidin-4-ones, as well as for 5,6-dimethyl-2-oxo- and 5,6-dimethyl-2-thioxothieno[2,3-d]pyrimidin-4-ones, were carried out at the HF and DFT levels. An analysis of the relative energies shows that the 2-oxo form or the related thioxo or selenoxo forms are energetically more favorable in tautomeric interconversions of all the compounds under study both in the gas phase and in solutions in ethanol, acetonitrile, and DMSO.
    19 schema:genre research_article
    20 schema:inLanguage en
    21 schema:isAccessibleForFree false
    22 schema:isPartOf N52cd77d7b62f45a0af37af3b0b0f00ab
    23 Nc13f3f4c349a4d8cb06b1767d3d0ac42
    24 sg:journal.1022309
    25 schema:name Quantum chemical studies of pyrimidin-4-ones 3. 2-Oxo(thioxo, selenoxo)pyrimidin-4-ones and 5,6-dimethyl-2-oxo(thioxo)thieno[2,3-d]pyrimidin-4-ones
    26 schema:pagination 350-354
    27 schema:productId N4eddc030b56241049503300ab718169c
    28 N694c5bd6f1db43768153fa888218ed3a
    29 N70b8e6f8e12a438cb2b497d470770a5a
    30 schema:sameAs https://app.dimensions.ai/details/publication/pub.1038761433
    31 https://doi.org/10.1007/s11172-014-0436-7
    32 schema:sdDatePublished 2019-04-10T13:22
    33 schema:sdLicense https://scigraph.springernature.com/explorer/license/
    34 schema:sdPublisher N02fba0b562b54605ad4957d8acad25cc
    35 schema:url http://link.springer.com/10.1007%2Fs11172-014-0436-7
    36 sgo:license sg:explorer/license/
    37 sgo:sdDataset articles
    38 rdf:type schema:ScholarlyArticle
    39 N02fba0b562b54605ad4957d8acad25cc schema:name Springer Nature - SN SciGraph project
    40 rdf:type schema:Organization
    41 N036327f24078442a9eb23e59439685ea rdf:first sg:person.015706066705.62
    42 rdf:rest rdf:nil
    43 N17552aaab24b45f39bd67b6eb06f3292 rdf:first sg:person.016614773551.45
    44 rdf:rest N751c5fc0ccb54fd89fa374185868bdf1
    45 N4eddc030b56241049503300ab718169c schema:name readcube_id
    46 schema:value b8a48b01d40e53fc49c6cf7bc5532bc93c680f4d77b6869f9bbd09b29247b96c
    47 rdf:type schema:PropertyValue
    48 N52cd77d7b62f45a0af37af3b0b0f00ab schema:volumeNumber 63
    49 rdf:type schema:PublicationVolume
    50 N694c5bd6f1db43768153fa888218ed3a schema:name doi
    51 schema:value 10.1007/s11172-014-0436-7
    52 rdf:type schema:PropertyValue
    53 N70b8e6f8e12a438cb2b497d470770a5a schema:name dimensions_id
    54 schema:value pub.1038761433
    55 rdf:type schema:PropertyValue
    56 N751c5fc0ccb54fd89fa374185868bdf1 rdf:first sg:person.010473055641.48
    57 rdf:rest Nf3e2df73ac2e40098d78751cdd3a71b4
    58 N9da42e3fd26d4f109489614d4c06d244 rdf:first sg:person.016151244107.99
    59 rdf:rest N17552aaab24b45f39bd67b6eb06f3292
    60 Nc13f3f4c349a4d8cb06b1767d3d0ac42 schema:issueNumber 2
    61 rdf:type schema:PublicationIssue
    62 Nf3e2df73ac2e40098d78751cdd3a71b4 rdf:first sg:person.016557000703.78
    63 rdf:rest N036327f24078442a9eb23e59439685ea
    64 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
    65 schema:name Chemical Sciences
    66 rdf:type schema:DefinedTerm
    67 anzsrc-for:0306 schema:inDefinedTermSet anzsrc-for:
    68 schema:name Physical Chemistry (incl. Structural)
    69 rdf:type schema:DefinedTerm
    70 sg:journal.1022309 schema:issn 1066-5285
    71 1573-9171
    72 schema:name Russian Chemical Bulletin
    73 rdf:type schema:Periodical
    74 sg:person.010473055641.48 schema:affiliation https://www.grid.ac/institutes/grid.4886.2
    75 schema:familyName Chuvylkin
    76 schema:givenName N. D.
    77 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010473055641.48
    78 rdf:type schema:Person
    79 sg:person.015706066705.62 schema:affiliation https://www.grid.ac/institutes/grid.419209.7
    80 schema:familyName Shakhidoyatov
    81 schema:givenName Kh. M.
    82 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015706066705.62
    83 rdf:type schema:Person
    84 sg:person.016151244107.99 schema:affiliation https://www.grid.ac/institutes/grid.419209.7
    85 schema:familyName Mamarakhmonov
    86 schema:givenName M. Kh.
    87 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016151244107.99
    88 rdf:type schema:Person
    89 sg:person.016557000703.78 schema:affiliation https://www.grid.ac/institutes/grid.419209.7
    90 schema:familyName Ashirmatov
    91 schema:givenName M. A.
    92 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016557000703.78
    93 rdf:type schema:Person
    94 sg:person.016614773551.45 schema:affiliation https://www.grid.ac/institutes/grid.4886.2
    95 schema:familyName Belen’kii
    96 schema:givenName L. I.
    97 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016614773551.45
    98 rdf:type schema:Person
    99 sg:pub.10.1007/bf01169964 schema:sameAs https://app.dimensions.ai/details/publication/pub.1011484408
    100 https://doi.org/10.1007/bf01169964
    101 rdf:type schema:CreativeWork
    102 sg:pub.10.1007/s10593-011-0677-4 schema:sameAs https://app.dimensions.ai/details/publication/pub.1019113361
    103 https://doi.org/10.1007/s10593-011-0677-4
    104 rdf:type schema:CreativeWork
    105 sg:pub.10.1007/s11172-005-0332-2 schema:sameAs https://app.dimensions.ai/details/publication/pub.1040773254
    106 https://doi.org/10.1007/s11172-005-0332-2
    107 rdf:type schema:CreativeWork
    108 sg:pub.10.1007/s11172-007-0229-3 schema:sameAs https://app.dimensions.ai/details/publication/pub.1026005341
    109 https://doi.org/10.1007/s11172-007-0229-3
    110 rdf:type schema:CreativeWork
    111 sg:pub.10.1007/s11172-011-0354-x schema:sameAs https://app.dimensions.ai/details/publication/pub.1004877063
    112 https://doi.org/10.1007/s11172-011-0354-x
    113 rdf:type schema:CreativeWork
    114 sg:pub.10.1023/a:1009501611921 schema:sameAs https://app.dimensions.ai/details/publication/pub.1001556840
    115 https://doi.org/10.1023/a:1009501611921
    116 rdf:type schema:CreativeWork
    117 sg:pub.10.1023/a:1012791718619 schema:sameAs https://app.dimensions.ai/details/publication/pub.1052660853
    118 https://doi.org/10.1023/a:1012791718619
    119 rdf:type schema:CreativeWork
    120 sg:pub.10.1023/a:1015024612380 schema:sameAs https://app.dimensions.ai/details/publication/pub.1005577299
    121 https://doi.org/10.1023/a:1015024612380
    122 rdf:type schema:CreativeWork
    123 sg:pub.10.1023/b:cohc.0000010649.76065.65 schema:sameAs https://app.dimensions.ai/details/publication/pub.1015988714
    124 https://doi.org/10.1023/b:cohc.0000010649.76065.65
    125 rdf:type schema:CreativeWork
    126 https://doi.org/10.1002/jhet.5570330414 schema:sameAs https://app.dimensions.ai/details/publication/pub.1015537708
    127 rdf:type schema:CreativeWork
    128 https://doi.org/10.1021/jo00120a012 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055967902
    129 rdf:type schema:CreativeWork
    130 https://doi.org/10.9734/acsj/2013/2966 schema:sameAs https://app.dimensions.ai/details/publication/pub.1074126468
    131 rdf:type schema:CreativeWork
    132 https://www.grid.ac/institutes/grid.419209.7 schema:alternateName Academy of Sciences Republic of Uzbekistan
    133 schema:name Academician S. Yu. Yunusov Institute of Chemistry of Plant Substances, Academy of Sciences Republic of Uzbekistan, 77 ul. Mirzo Ulu gbeka, 100170, Tashkent, Uzbekistan
    134 rdf:type schema:Organization
    135 https://www.grid.ac/institutes/grid.4886.2 schema:alternateName Russian Academy of Sciences
    136 schema:name N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation
    137 rdf:type schema:Organization
     




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


    ...