Thiocarbamoylation of 1,2,3,4-tetrahydroisoquinoline enamines with phenyl isothiocyanate View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2014-09

AUTHORS

O. V. Surikova, A. G. Mikhailovskii

ABSTRACT

Reactions of 1,3,3-trimethyl-3,4-dihydroisoquinoline and its benzo[f] derivative with phenyl isothiocyanate gave the corresponding enamino thioamides. Enamino ester, enamino amides, and enamino nitriles of the 1,2,3,4-tetrahydroisoquinoline series reacted with phenyl isothiocyanate in a similar way. The resulting enamino thioamides underwent acylation with acid chlorides at the β-carbon atom of the enamino fragment. The structure of the obtained enamino thioamides is stabilized by intramolecular H-bonding. More... »

PAGES

1306-1311

References to SciGraph publications

  • 1994-08. Synthesis and biological activity of substituted (3,3-dimethyl-1,2,3,4-tetrahydroisoquinolylidene-1) acetanilides and malonanilides in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 1988-07. Synthesis and acylation of tertiary enamines: 1,2,3,4-tetrahydroisoquinoline derivatives in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 1994-07. Reaction of enamines of the isocholine and phenanthridine series with oxalyl chloride in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2005-04. Symmetrical and Unsymmetrical Bis-1,1′-(3,4-dihydroisoquinolines) in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 1998-08. Synthesis and study of antiaggregative and hypotensive activity of condensed isoquinoline derivatives in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 2009-01. Synthesis of amides of 2-(3,3,7-trimethyl-3,4-dihydroisoquinolyl-1)ethanoic acid and their effects on arterial blood pressure in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 1992-03. Synthesis of 4-R-2,2-dimethyl-1,2-dihydrobenzo[f]isoquinolines and (2,2-dimethyl-1,2-dihydrobenzo[f]isoquinolylidene-4)acetic acid derivatives in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2008-06. Reactions of 2,3-dioxopyrrolo[2,1-a]isoquinolinecarboxylic acid esters and amides with nitrogen-centered nucleophiles in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • 1985-06. Synthesis and tautomerism of 1-substituted 3,3-dialkyl-3,4-dihydroisoquinolines in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2002-02. Properties of 4-Chloromethyl-2,2-dimethyl-1,2-dihydrobenzo[f]isoquinoline in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2013-10. Acylation reaction of the 3,3-dimethylisoquinoline series enaminonitrile and properties of 5,5-dimethyl- 2,3-dioxo-2,3,5,6-tetrahydropyrrolo[2,1-a]isoquinoline- 1-carbonitrile in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 1983-11. Synthesis of enamine derivatives of 3,4-dihydroisoquinoline in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • 2009-02. Synthesis of 2-(3,3-dimethyl-3,4-dihydroisoquinol-1-yl)propanoic acid amides and their influence on blood coagulation in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 2002-06. Chloromethyl and Aryloxymethyl 3,4-Dihydroisoquinoline Derivatives: Synthesis and Study of Antiaggregant and Antihypoxant Properties in PHARMACEUTICAL CHEMISTRY JOURNAL
  • 1989-09. Synthesis of enaminoamides of the 1,2,3,4-tetrahydroisoquinoline series in CHEMISTRY OF HETEROCYCLIC COMPOUNDS
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1134/s1070428014090127

    DOI

    http://dx.doi.org/10.1134/s1070428014090127

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1048956232


    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/2008/0202", 
            "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
            "name": "Atomic, Molecular, Nuclear, Particle and Plasma Physics", 
            "type": "DefinedTerm"
          }, 
          {
            "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/02", 
            "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
            "name": "Physical Sciences", 
            "type": "DefinedTerm"
          }
        ], 
        "author": [
          {
            "affiliation": {
              "alternateName": "Perm State Pharmaceutical Academy", 
              "id": "https://www.grid.ac/institutes/grid.445544.0", 
              "name": [
                "Perm State Pharmaceutical Academy, ul. Polevaya 2, 614990, Perm, Russia"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Surikova", 
            "givenName": "O. V.", 
            "id": "sg:person.07677646577.36", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07677646577.36"
            ], 
            "type": "Person"
          }, 
          {
            "affiliation": {
              "alternateName": "Perm State Pharmaceutical Academy", 
              "id": "https://www.grid.ac/institutes/grid.445544.0", 
              "name": [
                "Perm State Pharmaceutical Academy, ul. Polevaya 2, 614990, Perm, Russia"
              ], 
              "type": "Organization"
            }, 
            "familyName": "Mikhailovskii", 
            "givenName": "A. G.", 
            "id": "sg:person.012373303224.18", 
            "sameAs": [
              "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012373303224.18"
            ], 
            "type": "Person"
          }
        ], 
        "citation": [
          {
            "id": "sg:pub.10.1007/bf00515067", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1002044925", 
              "https://doi.org/10.1007/bf00515067"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf00515067", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1002044925", 
              "https://doi.org/10.1007/bf00515067"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1023/a:1020816304323", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1006314662", 
              "https://doi.org/10.1023/a:1020816304323"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1134/s1070428008060109", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1010527854", 
              "https://doi.org/10.1134/s1070428008060109"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf00529376", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1018771069", 
              "https://doi.org/10.1007/bf00529376"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf00529376", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1018771069", 
              "https://doi.org/10.1007/bf00529376"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf00515370", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1020622900", 
              "https://doi.org/10.1007/bf00515370"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf00515370", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1020622900", 
              "https://doi.org/10.1007/bf00515370"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf02465771", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1020642491", 
              "https://doi.org/10.1007/bf02465771"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf00633173", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1024588504", 
              "https://doi.org/10.1007/bf00633173"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf00633173", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1024588504", 
              "https://doi.org/10.1007/bf00633173"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1023/a:1015343426495", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1029813637", 
              "https://doi.org/10.1023/a:1015343426495"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf01169639", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1030779839", 
              "https://doi.org/10.1007/bf01169639"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf01169639", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1030779839", 
              "https://doi.org/10.1007/bf01169639"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf00487305", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1037073110", 
              "https://doi.org/10.1007/bf00487305"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf00487305", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1037073110", 
              "https://doi.org/10.1007/bf00487305"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/s11094-009-0221-3", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1039877374", 
              "https://doi.org/10.1007/s11094-009-0221-3"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/s11094-009-0250-y", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1042322661", 
              "https://doi.org/10.1007/s11094-009-0250-y"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/s10593-005-0174-8", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1043343485", 
              "https://doi.org/10.1007/s10593-005-0174-8"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/s10593-005-0174-8", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1043343485", 
              "https://doi.org/10.1007/s10593-005-0174-8"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/s10593-013-1334-x", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1047171255", 
              "https://doi.org/10.1007/s10593-013-1334-x"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf02219028", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1050003569", 
              "https://doi.org/10.1007/bf02219028"
            ], 
            "type": "CreativeWork"
          }, 
          {
            "id": "sg:pub.10.1007/bf02219028", 
            "sameAs": [
              "https://app.dimensions.ai/details/publication/pub.1050003569", 
              "https://doi.org/10.1007/bf02219028"
            ], 
            "type": "CreativeWork"
          }
        ], 
        "datePublished": "2014-09", 
        "datePublishedReg": "2014-09-01", 
        "description": "Reactions of 1,3,3-trimethyl-3,4-dihydroisoquinoline and its benzo[f] derivative with phenyl isothiocyanate gave the corresponding enamino thioamides. Enamino ester, enamino amides, and enamino nitriles of the 1,2,3,4-tetrahydroisoquinoline series reacted with phenyl isothiocyanate in a similar way. The resulting enamino thioamides underwent acylation with acid chlorides at the \u03b2-carbon atom of the enamino fragment. The structure of the obtained enamino thioamides is stabilized by intramolecular H-bonding.", 
        "genre": "research_article", 
        "id": "sg:pub.10.1134/s1070428014090127", 
        "inLanguage": [
          "en"
        ], 
        "isAccessibleForFree": false, 
        "isPartOf": [
          {
            "id": "sg:journal.1136317", 
            "issn": [
              "1070-4280", 
              "1608-3393"
            ], 
            "name": "Russian Journal of Organic Chemistry", 
            "type": "Periodical"
          }, 
          {
            "issueNumber": "9", 
            "type": "PublicationIssue"
          }, 
          {
            "type": "PublicationVolume", 
            "volumeNumber": "50"
          }
        ], 
        "name": "Thiocarbamoylation of 1,2,3,4-tetrahydroisoquinoline enamines with phenyl isothiocyanate", 
        "pagination": "1306-1311", 
        "productId": [
          {
            "name": "readcube_id", 
            "type": "PropertyValue", 
            "value": [
              "e9383d7e751fa84394292365cbc1d1aca67c9806052d57b9c17385fd5410ef38"
            ]
          }, 
          {
            "name": "doi", 
            "type": "PropertyValue", 
            "value": [
              "10.1134/s1070428014090127"
            ]
          }, 
          {
            "name": "dimensions_id", 
            "type": "PropertyValue", 
            "value": [
              "pub.1048956232"
            ]
          }
        ], 
        "sameAs": [
          "https://doi.org/10.1134/s1070428014090127", 
          "https://app.dimensions.ai/details/publication/pub.1048956232"
        ], 
        "sdDataset": "articles", 
        "sdDatePublished": "2019-04-11T01:59", 
        "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_8700_00000508.jsonl", 
        "type": "ScholarlyArticle", 
        "url": "http://link.springer.com/10.1134%2FS1070428014090127"
      }
    ]
     

    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.10.1134/s1070428014090127'

    N-Triples is a line-based linked data format ideal for batch operations.

    curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1134/s1070428014090127'

    Turtle is a human-readable linked data format.

    curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1134/s1070428014090127'

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

    curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1134/s1070428014090127'


     

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

    128 TRIPLES      21 PREDICATES      42 URIs      19 LITERALS      7 BLANK NODES

    Subject Predicate Object
    1 sg:pub.10.1134/s1070428014090127 schema:about anzsrc-for:02
    2 anzsrc-for:0202
    3 schema:author N99651601b22b464bb8fdb6059b1bc544
    4 schema:citation sg:pub.10.1007/bf00487305
    5 sg:pub.10.1007/bf00515067
    6 sg:pub.10.1007/bf00515370
    7 sg:pub.10.1007/bf00529376
    8 sg:pub.10.1007/bf00633173
    9 sg:pub.10.1007/bf01169639
    10 sg:pub.10.1007/bf02219028
    11 sg:pub.10.1007/bf02465771
    12 sg:pub.10.1007/s10593-005-0174-8
    13 sg:pub.10.1007/s10593-013-1334-x
    14 sg:pub.10.1007/s11094-009-0221-3
    15 sg:pub.10.1007/s11094-009-0250-y
    16 sg:pub.10.1023/a:1015343426495
    17 sg:pub.10.1023/a:1020816304323
    18 sg:pub.10.1134/s1070428008060109
    19 schema:datePublished 2014-09
    20 schema:datePublishedReg 2014-09-01
    21 schema:description Reactions of 1,3,3-trimethyl-3,4-dihydroisoquinoline and its benzo[f] derivative with phenyl isothiocyanate gave the corresponding enamino thioamides. Enamino ester, enamino amides, and enamino nitriles of the 1,2,3,4-tetrahydroisoquinoline series reacted with phenyl isothiocyanate in a similar way. The resulting enamino thioamides underwent acylation with acid chlorides at the β-carbon atom of the enamino fragment. The structure of the obtained enamino thioamides is stabilized by intramolecular H-bonding.
    22 schema:genre research_article
    23 schema:inLanguage en
    24 schema:isAccessibleForFree false
    25 schema:isPartOf N9a2a44213a6849fa809b9d31e10c021a
    26 Ne1853748fd264995b2d5c389931b26ce
    27 sg:journal.1136317
    28 schema:name Thiocarbamoylation of 1,2,3,4-tetrahydroisoquinoline enamines with phenyl isothiocyanate
    29 schema:pagination 1306-1311
    30 schema:productId N038377246a644199a7be92885f1d6d69
    31 N1c67e3a52d044d97a9123c2714621ae2
    32 N49945d8b80ea4028806f3cd86c414732
    33 schema:sameAs https://app.dimensions.ai/details/publication/pub.1048956232
    34 https://doi.org/10.1134/s1070428014090127
    35 schema:sdDatePublished 2019-04-11T01:59
    36 schema:sdLicense https://scigraph.springernature.com/explorer/license/
    37 schema:sdPublisher Nd690b21307e047c7abed9d30f207e146
    38 schema:url http://link.springer.com/10.1134%2FS1070428014090127
    39 sgo:license sg:explorer/license/
    40 sgo:sdDataset articles
    41 rdf:type schema:ScholarlyArticle
    42 N038377246a644199a7be92885f1d6d69 schema:name dimensions_id
    43 schema:value pub.1048956232
    44 rdf:type schema:PropertyValue
    45 N1c67e3a52d044d97a9123c2714621ae2 schema:name doi
    46 schema:value 10.1134/s1070428014090127
    47 rdf:type schema:PropertyValue
    48 N4734602e6dcc480fa78aaff864bf6775 rdf:first sg:person.012373303224.18
    49 rdf:rest rdf:nil
    50 N49945d8b80ea4028806f3cd86c414732 schema:name readcube_id
    51 schema:value e9383d7e751fa84394292365cbc1d1aca67c9806052d57b9c17385fd5410ef38
    52 rdf:type schema:PropertyValue
    53 N99651601b22b464bb8fdb6059b1bc544 rdf:first sg:person.07677646577.36
    54 rdf:rest N4734602e6dcc480fa78aaff864bf6775
    55 N9a2a44213a6849fa809b9d31e10c021a schema:issueNumber 9
    56 rdf:type schema:PublicationIssue
    57 Nd690b21307e047c7abed9d30f207e146 schema:name Springer Nature - SN SciGraph project
    58 rdf:type schema:Organization
    59 Ne1853748fd264995b2d5c389931b26ce schema:volumeNumber 50
    60 rdf:type schema:PublicationVolume
    61 anzsrc-for:02 schema:inDefinedTermSet anzsrc-for:
    62 schema:name Physical Sciences
    63 rdf:type schema:DefinedTerm
    64 anzsrc-for:0202 schema:inDefinedTermSet anzsrc-for:
    65 schema:name Atomic, Molecular, Nuclear, Particle and Plasma Physics
    66 rdf:type schema:DefinedTerm
    67 sg:journal.1136317 schema:issn 1070-4280
    68 1608-3393
    69 schema:name Russian Journal of Organic Chemistry
    70 rdf:type schema:Periodical
    71 sg:person.012373303224.18 schema:affiliation https://www.grid.ac/institutes/grid.445544.0
    72 schema:familyName Mikhailovskii
    73 schema:givenName A. G.
    74 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012373303224.18
    75 rdf:type schema:Person
    76 sg:person.07677646577.36 schema:affiliation https://www.grid.ac/institutes/grid.445544.0
    77 schema:familyName Surikova
    78 schema:givenName O. V.
    79 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07677646577.36
    80 rdf:type schema:Person
    81 sg:pub.10.1007/bf00487305 schema:sameAs https://app.dimensions.ai/details/publication/pub.1037073110
    82 https://doi.org/10.1007/bf00487305
    83 rdf:type schema:CreativeWork
    84 sg:pub.10.1007/bf00515067 schema:sameAs https://app.dimensions.ai/details/publication/pub.1002044925
    85 https://doi.org/10.1007/bf00515067
    86 rdf:type schema:CreativeWork
    87 sg:pub.10.1007/bf00515370 schema:sameAs https://app.dimensions.ai/details/publication/pub.1020622900
    88 https://doi.org/10.1007/bf00515370
    89 rdf:type schema:CreativeWork
    90 sg:pub.10.1007/bf00529376 schema:sameAs https://app.dimensions.ai/details/publication/pub.1018771069
    91 https://doi.org/10.1007/bf00529376
    92 rdf:type schema:CreativeWork
    93 sg:pub.10.1007/bf00633173 schema:sameAs https://app.dimensions.ai/details/publication/pub.1024588504
    94 https://doi.org/10.1007/bf00633173
    95 rdf:type schema:CreativeWork
    96 sg:pub.10.1007/bf01169639 schema:sameAs https://app.dimensions.ai/details/publication/pub.1030779839
    97 https://doi.org/10.1007/bf01169639
    98 rdf:type schema:CreativeWork
    99 sg:pub.10.1007/bf02219028 schema:sameAs https://app.dimensions.ai/details/publication/pub.1050003569
    100 https://doi.org/10.1007/bf02219028
    101 rdf:type schema:CreativeWork
    102 sg:pub.10.1007/bf02465771 schema:sameAs https://app.dimensions.ai/details/publication/pub.1020642491
    103 https://doi.org/10.1007/bf02465771
    104 rdf:type schema:CreativeWork
    105 sg:pub.10.1007/s10593-005-0174-8 schema:sameAs https://app.dimensions.ai/details/publication/pub.1043343485
    106 https://doi.org/10.1007/s10593-005-0174-8
    107 rdf:type schema:CreativeWork
    108 sg:pub.10.1007/s10593-013-1334-x schema:sameAs https://app.dimensions.ai/details/publication/pub.1047171255
    109 https://doi.org/10.1007/s10593-013-1334-x
    110 rdf:type schema:CreativeWork
    111 sg:pub.10.1007/s11094-009-0221-3 schema:sameAs https://app.dimensions.ai/details/publication/pub.1039877374
    112 https://doi.org/10.1007/s11094-009-0221-3
    113 rdf:type schema:CreativeWork
    114 sg:pub.10.1007/s11094-009-0250-y schema:sameAs https://app.dimensions.ai/details/publication/pub.1042322661
    115 https://doi.org/10.1007/s11094-009-0250-y
    116 rdf:type schema:CreativeWork
    117 sg:pub.10.1023/a:1015343426495 schema:sameAs https://app.dimensions.ai/details/publication/pub.1029813637
    118 https://doi.org/10.1023/a:1015343426495
    119 rdf:type schema:CreativeWork
    120 sg:pub.10.1023/a:1020816304323 schema:sameAs https://app.dimensions.ai/details/publication/pub.1006314662
    121 https://doi.org/10.1023/a:1020816304323
    122 rdf:type schema:CreativeWork
    123 sg:pub.10.1134/s1070428008060109 schema:sameAs https://app.dimensions.ai/details/publication/pub.1010527854
    124 https://doi.org/10.1134/s1070428008060109
    125 rdf:type schema:CreativeWork
    126 https://www.grid.ac/institutes/grid.445544.0 schema:alternateName Perm State Pharmaceutical Academy
    127 schema:name Perm State Pharmaceutical Academy, ul. Polevaya 2, 614990, Perm, Russia
    128 rdf:type schema:Organization
     




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


    ...