Synthesis of functionalized triazolo[1,5-a]pyrimidine derivatives View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2018-01

AUTHORS

Natal’ya V. Chechina, Nadezhda N. Kolos, Irina V. Omelchenko, Vladimir I. Musatov

ABSTRACT

New triazolo[1,5-a]pyrimidines containing aroyl and acetyl or ester groups in the pyrimidine ring were synthesized in a process related to the Biginelli-like reaction, using hydrates of arylglyoxals, β-dicarbonyl compounds, and 1H-1,2,4-triazol-5-amine. Reaction was carried out in either sequential or one-pot procedure.

PAGES

58-62

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-018-2230-1

DOI

http://dx.doi.org/10.1007/s10593-018-2230-1

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1101141709


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/2008/0305", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Organic Chemistry", 
        "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": "University of Kharkiv", 
          "id": "https://www.grid.ac/institutes/grid.18999.30", 
          "name": [
            "V. N. Karazin Kharkiv National University, 4 Svobody Sq., 61022, Kharkiv, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Chechina", 
        "givenName": "Natal\u2019ya V.", 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "University of Kharkiv", 
          "id": "https://www.grid.ac/institutes/grid.18999.30", 
          "name": [
            "V. N. Karazin Kharkiv National University, 4 Svobody Sq., 61022, Kharkiv, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Kolos", 
        "givenName": "Nadezhda N.", 
        "id": "sg:person.012470111723.62", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012470111723.62"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "National Academy of Sciences of Ukraine", 
          "id": "https://www.grid.ac/institutes/grid.418751.e", 
          "name": [
            "STC \u201cInstitute of Single Crystals\u201d, National Academy of Sciences of Ukraine, 60 Nauky Ave., 61072, Kharkiv, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Omelchenko", 
        "givenName": "Irina V.", 
        "id": "sg:person.0702540414.77", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0702540414.77"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "National Academy of Sciences of Ukraine", 
          "id": "https://www.grid.ac/institutes/grid.418751.e", 
          "name": [
            "STC \u201cInstitute of Single Crystals\u201d, National Academy of Sciences of Ukraine, 60 Nauky Ave., 61072, Kharkiv, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Musatov", 
        "givenName": "Vladimir I.", 
        "id": "sg:person.011375757463.27", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011375757463.27"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "https://doi.org/10.1016/s0040-4020(01)87971-0", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1001645281"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.3390/molecules17011074", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1009459397"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.3390/molecules17011074", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1009459397"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570450527", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1016140351"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570450527", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1016140351"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s10593-011-0864-3", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1017616093", 
          "https://doi.org/10.1007/s10593-011-0864-3"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570360131", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1019177921"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570360131", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1019177921"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/bf03245937", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1020187177", 
          "https://doi.org/10.1007/bf03245937"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.ejmech.2007.07.012", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1020942621"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.ejmech.2009.09.018", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1023320618"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1107/s0108767307043930", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1027786902"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s10593-016-1818-6", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1029103659", 
          "https://doi.org/10.1007/s10593-016-1818-6"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.ejmech.2010.08.022", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1029448312"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/anie.201005336", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1029500591"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s10593-012-1030-2", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1032873981", 
          "https://doi.org/10.1007/s10593-012-1030-2"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.tet.2011.09.138", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1035035648"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.molcata.2013.04.014", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1037893028"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.dit.2013.05.010", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1039173438"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/1521-3773(20000915)39:18<3168::aid-anie3168>3.0.co;2-u", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1039526894"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1107/s0021889808042726", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1044824966"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.bmcl.2010.06.058", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1051445387"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/bi100119t", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055203010"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/bi100119t", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055203010"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm100421n", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055951642"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm100421n", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055951642"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.2174/0929867023368719", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1069159849"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2018-01", 
    "datePublishedReg": "2018-01-01", 
    "description": "New triazolo[1,5-a]pyrimidines containing aroyl and acetyl or ester groups in the pyrimidine ring were synthesized in a process related to the Biginelli-like reaction, using hydrates of arylglyoxals, \u03b2-dicarbonyl compounds, and 1H-1,2,4-triazol-5-amine. Reaction was carried out in either sequential or one-pot procedure.", 
    "genre": "research_article", 
    "id": "sg:pub.10.1007/s10593-018-2230-1", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1356886", 
        "issn": [
          "0009-3122", 
          "1573-8353"
        ], 
        "name": "Chemistry of Heterocyclic Compounds", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "1", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "54"
      }
    ], 
    "name": "Synthesis of functionalized triazolo[1,5-a]pyrimidine derivatives", 
    "pagination": "58-62", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "aa20e840ee9a4228b504a99333f90cb2d05956af970602dc6a08841b2458aab1"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s10593-018-2230-1"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1101141709"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s10593-018-2230-1", 
      "https://app.dimensions.ai/details/publication/pub.1101141709"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-11T09:32", 
    "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/v90/0000000346_0000000346/records_99806_00000004.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://link.springer.com/10.1007%2Fs10593-018-2230-1"
  }
]
 

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/s10593-018-2230-1'

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/s10593-018-2230-1'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s10593-018-2230-1'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s10593-018-2230-1'


 

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

154 TRIPLES      21 PREDICATES      49 URIs      19 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s10593-018-2230-1 schema:about anzsrc-for:03
2 anzsrc-for:0305
3 schema:author Nef0d6738b37b4bbdad2d21f74067efcf
4 schema:citation sg:pub.10.1007/bf03245937
5 sg:pub.10.1007/s10593-011-0864-3
6 sg:pub.10.1007/s10593-012-1030-2
7 sg:pub.10.1007/s10593-016-1818-6
8 https://doi.org/10.1002/1521-3773(20000915)39:18<3168::aid-anie3168>3.0.co;2-u
9 https://doi.org/10.1002/anie.201005336
10 https://doi.org/10.1002/jhet.5570360131
11 https://doi.org/10.1002/jhet.5570450527
12 https://doi.org/10.1016/j.bmcl.2010.06.058
13 https://doi.org/10.1016/j.dit.2013.05.010
14 https://doi.org/10.1016/j.ejmech.2007.07.012
15 https://doi.org/10.1016/j.ejmech.2009.09.018
16 https://doi.org/10.1016/j.ejmech.2010.08.022
17 https://doi.org/10.1016/j.molcata.2013.04.014
18 https://doi.org/10.1016/j.tet.2011.09.138
19 https://doi.org/10.1016/s0040-4020(01)87971-0
20 https://doi.org/10.1021/bi100119t
21 https://doi.org/10.1021/jm100421n
22 https://doi.org/10.1107/s0021889808042726
23 https://doi.org/10.1107/s0108767307043930
24 https://doi.org/10.2174/0929867023368719
25 https://doi.org/10.3390/molecules17011074
26 schema:datePublished 2018-01
27 schema:datePublishedReg 2018-01-01
28 schema:description New triazolo[1,5-a]pyrimidines containing aroyl and acetyl or ester groups in the pyrimidine ring were synthesized in a process related to the Biginelli-like reaction, using hydrates of arylglyoxals, β-dicarbonyl compounds, and 1H-1,2,4-triazol-5-amine. Reaction was carried out in either sequential or one-pot procedure.
29 schema:genre research_article
30 schema:inLanguage en
31 schema:isAccessibleForFree false
32 schema:isPartOf N632ef2dee34347f29fd61bfdae943e04
33 Nf26ce974a002445a964e0d050deed7c6
34 sg:journal.1356886
35 schema:name Synthesis of functionalized triazolo[1,5-a]pyrimidine derivatives
36 schema:pagination 58-62
37 schema:productId N5fa6a195301e495e83bc9990cbcfd052
38 Na4cc8e51df64435680d16804e4d68653
39 Nc1f71bc0bc8c4cf38bd26411d7ee24be
40 schema:sameAs https://app.dimensions.ai/details/publication/pub.1101141709
41 https://doi.org/10.1007/s10593-018-2230-1
42 schema:sdDatePublished 2019-04-11T09:32
43 schema:sdLicense https://scigraph.springernature.com/explorer/license/
44 schema:sdPublisher Na38e52d9405848a1b98cdae528efc91e
45 schema:url https://link.springer.com/10.1007%2Fs10593-018-2230-1
46 sgo:license sg:explorer/license/
47 sgo:sdDataset articles
48 rdf:type schema:ScholarlyArticle
49 N4bb2280346eb41d19d61dad741252f5e schema:affiliation https://www.grid.ac/institutes/grid.18999.30
50 schema:familyName Chechina
51 schema:givenName Natal’ya V.
52 rdf:type schema:Person
53 N5686fed50e07483fb0772fd805582ffc rdf:first sg:person.012470111723.62
54 rdf:rest N68cf9cb9b6464a4f8ff477041bf6dee0
55 N5fa6a195301e495e83bc9990cbcfd052 schema:name doi
56 schema:value 10.1007/s10593-018-2230-1
57 rdf:type schema:PropertyValue
58 N632ef2dee34347f29fd61bfdae943e04 schema:volumeNumber 54
59 rdf:type schema:PublicationVolume
60 N68cf9cb9b6464a4f8ff477041bf6dee0 rdf:first sg:person.0702540414.77
61 rdf:rest Na160b09dc6174d45befa50fa6a7486e8
62 Na160b09dc6174d45befa50fa6a7486e8 rdf:first sg:person.011375757463.27
63 rdf:rest rdf:nil
64 Na38e52d9405848a1b98cdae528efc91e schema:name Springer Nature - SN SciGraph project
65 rdf:type schema:Organization
66 Na4cc8e51df64435680d16804e4d68653 schema:name dimensions_id
67 schema:value pub.1101141709
68 rdf:type schema:PropertyValue
69 Nc1f71bc0bc8c4cf38bd26411d7ee24be schema:name readcube_id
70 schema:value aa20e840ee9a4228b504a99333f90cb2d05956af970602dc6a08841b2458aab1
71 rdf:type schema:PropertyValue
72 Nef0d6738b37b4bbdad2d21f74067efcf rdf:first N4bb2280346eb41d19d61dad741252f5e
73 rdf:rest N5686fed50e07483fb0772fd805582ffc
74 Nf26ce974a002445a964e0d050deed7c6 schema:issueNumber 1
75 rdf:type schema:PublicationIssue
76 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
77 schema:name Chemical Sciences
78 rdf:type schema:DefinedTerm
79 anzsrc-for:0305 schema:inDefinedTermSet anzsrc-for:
80 schema:name Organic Chemistry
81 rdf:type schema:DefinedTerm
82 sg:journal.1356886 schema:issn 0009-3122
83 1573-8353
84 schema:name Chemistry of Heterocyclic Compounds
85 rdf:type schema:Periodical
86 sg:person.011375757463.27 schema:affiliation https://www.grid.ac/institutes/grid.418751.e
87 schema:familyName Musatov
88 schema:givenName Vladimir I.
89 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011375757463.27
90 rdf:type schema:Person
91 sg:person.012470111723.62 schema:affiliation https://www.grid.ac/institutes/grid.18999.30
92 schema:familyName Kolos
93 schema:givenName Nadezhda N.
94 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012470111723.62
95 rdf:type schema:Person
96 sg:person.0702540414.77 schema:affiliation https://www.grid.ac/institutes/grid.418751.e
97 schema:familyName Omelchenko
98 schema:givenName Irina V.
99 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0702540414.77
100 rdf:type schema:Person
101 sg:pub.10.1007/bf03245937 schema:sameAs https://app.dimensions.ai/details/publication/pub.1020187177
102 https://doi.org/10.1007/bf03245937
103 rdf:type schema:CreativeWork
104 sg:pub.10.1007/s10593-011-0864-3 schema:sameAs https://app.dimensions.ai/details/publication/pub.1017616093
105 https://doi.org/10.1007/s10593-011-0864-3
106 rdf:type schema:CreativeWork
107 sg:pub.10.1007/s10593-012-1030-2 schema:sameAs https://app.dimensions.ai/details/publication/pub.1032873981
108 https://doi.org/10.1007/s10593-012-1030-2
109 rdf:type schema:CreativeWork
110 sg:pub.10.1007/s10593-016-1818-6 schema:sameAs https://app.dimensions.ai/details/publication/pub.1029103659
111 https://doi.org/10.1007/s10593-016-1818-6
112 rdf:type schema:CreativeWork
113 https://doi.org/10.1002/1521-3773(20000915)39:18<3168::aid-anie3168>3.0.co;2-u schema:sameAs https://app.dimensions.ai/details/publication/pub.1039526894
114 rdf:type schema:CreativeWork
115 https://doi.org/10.1002/anie.201005336 schema:sameAs https://app.dimensions.ai/details/publication/pub.1029500591
116 rdf:type schema:CreativeWork
117 https://doi.org/10.1002/jhet.5570360131 schema:sameAs https://app.dimensions.ai/details/publication/pub.1019177921
118 rdf:type schema:CreativeWork
119 https://doi.org/10.1002/jhet.5570450527 schema:sameAs https://app.dimensions.ai/details/publication/pub.1016140351
120 rdf:type schema:CreativeWork
121 https://doi.org/10.1016/j.bmcl.2010.06.058 schema:sameAs https://app.dimensions.ai/details/publication/pub.1051445387
122 rdf:type schema:CreativeWork
123 https://doi.org/10.1016/j.dit.2013.05.010 schema:sameAs https://app.dimensions.ai/details/publication/pub.1039173438
124 rdf:type schema:CreativeWork
125 https://doi.org/10.1016/j.ejmech.2007.07.012 schema:sameAs https://app.dimensions.ai/details/publication/pub.1020942621
126 rdf:type schema:CreativeWork
127 https://doi.org/10.1016/j.ejmech.2009.09.018 schema:sameAs https://app.dimensions.ai/details/publication/pub.1023320618
128 rdf:type schema:CreativeWork
129 https://doi.org/10.1016/j.ejmech.2010.08.022 schema:sameAs https://app.dimensions.ai/details/publication/pub.1029448312
130 rdf:type schema:CreativeWork
131 https://doi.org/10.1016/j.molcata.2013.04.014 schema:sameAs https://app.dimensions.ai/details/publication/pub.1037893028
132 rdf:type schema:CreativeWork
133 https://doi.org/10.1016/j.tet.2011.09.138 schema:sameAs https://app.dimensions.ai/details/publication/pub.1035035648
134 rdf:type schema:CreativeWork
135 https://doi.org/10.1016/s0040-4020(01)87971-0 schema:sameAs https://app.dimensions.ai/details/publication/pub.1001645281
136 rdf:type schema:CreativeWork
137 https://doi.org/10.1021/bi100119t schema:sameAs https://app.dimensions.ai/details/publication/pub.1055203010
138 rdf:type schema:CreativeWork
139 https://doi.org/10.1021/jm100421n schema:sameAs https://app.dimensions.ai/details/publication/pub.1055951642
140 rdf:type schema:CreativeWork
141 https://doi.org/10.1107/s0021889808042726 schema:sameAs https://app.dimensions.ai/details/publication/pub.1044824966
142 rdf:type schema:CreativeWork
143 https://doi.org/10.1107/s0108767307043930 schema:sameAs https://app.dimensions.ai/details/publication/pub.1027786902
144 rdf:type schema:CreativeWork
145 https://doi.org/10.2174/0929867023368719 schema:sameAs https://app.dimensions.ai/details/publication/pub.1069159849
146 rdf:type schema:CreativeWork
147 https://doi.org/10.3390/molecules17011074 schema:sameAs https://app.dimensions.ai/details/publication/pub.1009459397
148 rdf:type schema:CreativeWork
149 https://www.grid.ac/institutes/grid.18999.30 schema:alternateName University of Kharkiv
150 schema:name V. N. Karazin Kharkiv National University, 4 Svobody Sq., 61022, Kharkiv, Ukraine
151 rdf:type schema:Organization
152 https://www.grid.ac/institutes/grid.418751.e schema:alternateName National Academy of Sciences of Ukraine
153 schema:name STC “Institute of Single Crystals”, National Academy of Sciences of Ukraine, 60 Nauky Ave., 61072, Kharkiv, Ukraine
154 rdf:type schema:Organization
 




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


...