Synthesis of derivatives of 2-aminoimidazole and 2-iminoimidazolidine by cyclization of 1-aryl-2-(4,6-dimethylpyrimidin-2-yl)guanidines with α-bromocarbonyl compounds View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2011-04

AUTHORS

A. S. Shestakov, I. S. Bushmarinov, O. E. Sidorenko, Kh. S. Shikhaliev, M. Yu. Antipin

ABSTRACT

Cyclization of 1-aryl-2-(4,6-dimethylpyrimidin-2-yl)guanidines with α-bromoacetophenone and ethyl bromoacetate gave derivatives of 1,4-diphenyl-1H-imidazole-2-amine and 2-amino-1-phenylimidazolidin- 4-one respectively. The mechanism of the reaction was determined on the basis of quantum-chemical calculations, NOESY NMR spectroscopy, and X-ray crystallography.

PAGES

82-89

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-011-0723-2

DOI

http://dx.doi.org/10.1007/s10593-011-0723-2

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1014350135


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": "Voronezh State University", 
          "id": "https://www.grid.ac/institutes/grid.20567.36", 
          "name": [
            "Voronezh State University, Universitestskaya Pl., 1, 394006, Voronezh, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Shestakov", 
        "givenName": "A. S.", 
        "id": "sg:person.010236335635.38", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010236335635.38"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "A. N. Nesmeyanov Institute of Organoelement Compounds", 
          "id": "https://www.grid.ac/institutes/grid.431939.5", 
          "name": [
            "A. N. Nesmeyanov Institute of Organoelement Compounds, 28 Vavilova Str., 119991, Moscow, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Bushmarinov", 
        "givenName": "I. S.", 
        "id": "sg:person.01335445233.59", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01335445233.59"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Voronezh State University", 
          "id": "https://www.grid.ac/institutes/grid.20567.36", 
          "name": [
            "Voronezh State University, Universitestskaya Pl., 1, 394006, Voronezh, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Sidorenko", 
        "givenName": "O. E.", 
        "id": "sg:person.015517326524.13", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015517326524.13"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Voronezh State University", 
          "id": "https://www.grid.ac/institutes/grid.20567.36", 
          "name": [
            "Voronezh State University, Universitestskaya Pl., 1, 394006, Voronezh, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Shikhaliev", 
        "givenName": "Kh. S.", 
        "id": "sg:person.012501266731.37", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012501266731.37"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "A. N. Nesmeyanov Institute of Organoelement Compounds", 
          "id": "https://www.grid.ac/institutes/grid.431939.5", 
          "name": [
            "A. N. Nesmeyanov Institute of Organoelement Compounds, 28 Vavilova Str., 119991, Moscow, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Antipin", 
        "givenName": "M. Yu.", 
        "id": "sg:person.010142146727.55", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010142146727.55"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "https://doi.org/10.1002/jhet.5570020106", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1002769892"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570020106", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1002769892"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/cber.19610941207", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1010527679"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1246/bcsj.56.3703", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1019436657"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1248/cpb.32.4666", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1026862237"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1107/s0108767307043930", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1027786902"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570250119", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1047677478"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570250119", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1047677478"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1248/cpb.19.2284", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1049976355"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/bf00486967", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1052115694", 
          "https://doi.org/10.1007/bf00486967"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/bf00486967", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1052115694", 
          "https://doi.org/10.1007/bf00486967"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/bf00512966", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1052690454", 
          "https://doi.org/10.1007/bf00512966"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/bf00512966", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1052690454", 
          "https://doi.org/10.1007/bf00512966"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/cc700143n", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055228269"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/cc700143n", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055228269"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm00316a003", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055943104"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm9900321", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055959336"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm9900321", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055959336"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm990049j", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055959350"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm990049j", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055959350"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jo00103a021", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055966752"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jo8008758", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056032458"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jo8008758", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056032458"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/np020050c", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056228561"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/np020050c", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056228561"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/np0305223", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056229275"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/np0305223", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056229275"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ol062421c", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056248634"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ol062421c", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056248634"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2011-04", 
    "datePublishedReg": "2011-04-01", 
    "description": "Cyclization of 1-aryl-2-(4,6-dimethylpyrimidin-2-yl)guanidines with \u03b1-bromoacetophenone and ethyl bromoacetate gave derivatives of 1,4-diphenyl-1H-imidazole-2-amine and 2-amino-1-phenylimidazolidin- 4-one respectively. The mechanism of the reaction was determined on the basis of quantum-chemical calculations, NOESY NMR spectroscopy, and X-ray crystallography.", 
    "genre": "research_article", 
    "id": "sg:pub.10.1007/s10593-011-0723-2", 
    "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": "47"
      }
    ], 
    "name": "Synthesis of derivatives of 2-aminoimidazole and 2-iminoimidazolidine by cyclization of 1-aryl-2-(4,6-dimethylpyrimidin-2-yl)guanidines with \u03b1-bromocarbonyl compounds", 
    "pagination": "82-89", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "445cde802ff6b0c42318b5c378ce3dced3333329c01082575f8af3027b134692"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s10593-011-0723-2"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1014350135"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s10593-011-0723-2", 
      "https://app.dimensions.ai/details/publication/pub.1014350135"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-10T13:16", 
    "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_00000511.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "http://link.springer.com/10.1007%2Fs10593-011-0723-2"
  }
]
 

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/s10593-011-0723-2'

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/s10593-011-0723-2'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s10593-011-0723-2'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s10593-011-0723-2'


 

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

148 TRIPLES      21 PREDICATES      45 URIs      19 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s10593-011-0723-2 schema:about anzsrc-for:02
2 anzsrc-for:0202
3 schema:author Naedcdab67d064cdcb5e2cc7254b62626
4 schema:citation sg:pub.10.1007/bf00486967
5 sg:pub.10.1007/bf00512966
6 https://doi.org/10.1002/cber.19610941207
7 https://doi.org/10.1002/jhet.5570020106
8 https://doi.org/10.1002/jhet.5570250119
9 https://doi.org/10.1021/cc700143n
10 https://doi.org/10.1021/jm00316a003
11 https://doi.org/10.1021/jm9900321
12 https://doi.org/10.1021/jm990049j
13 https://doi.org/10.1021/jo00103a021
14 https://doi.org/10.1021/jo8008758
15 https://doi.org/10.1021/np020050c
16 https://doi.org/10.1021/np0305223
17 https://doi.org/10.1021/ol062421c
18 https://doi.org/10.1107/s0108767307043930
19 https://doi.org/10.1246/bcsj.56.3703
20 https://doi.org/10.1248/cpb.19.2284
21 https://doi.org/10.1248/cpb.32.4666
22 schema:datePublished 2011-04
23 schema:datePublishedReg 2011-04-01
24 schema:description Cyclization of 1-aryl-2-(4,6-dimethylpyrimidin-2-yl)guanidines with α-bromoacetophenone and ethyl bromoacetate gave derivatives of 1,4-diphenyl-1H-imidazole-2-amine and 2-amino-1-phenylimidazolidin- 4-one respectively. The mechanism of the reaction was determined on the basis of quantum-chemical calculations, NOESY NMR spectroscopy, and X-ray crystallography.
25 schema:genre research_article
26 schema:inLanguage en
27 schema:isAccessibleForFree false
28 schema:isPartOf N5600c22fac1e4fad84a6647b38e8d2f6
29 N5d247cb34b2743cdb250f70e2be8b795
30 sg:journal.1356886
31 schema:name Synthesis of derivatives of 2-aminoimidazole and 2-iminoimidazolidine by cyclization of 1-aryl-2-(4,6-dimethylpyrimidin-2-yl)guanidines with α-bromocarbonyl compounds
32 schema:pagination 82-89
33 schema:productId N07a179c12c534c2a8bddb52598baba3d
34 N609941dff205400ebb7358eb5517d456
35 Ne5b276577af049b6aaf7152e0f82d15a
36 schema:sameAs https://app.dimensions.ai/details/publication/pub.1014350135
37 https://doi.org/10.1007/s10593-011-0723-2
38 schema:sdDatePublished 2019-04-10T13:16
39 schema:sdLicense https://scigraph.springernature.com/explorer/license/
40 schema:sdPublisher N2c5c2ed42f3e41f1b65eb386151ae1c5
41 schema:url http://link.springer.com/10.1007%2Fs10593-011-0723-2
42 sgo:license sg:explorer/license/
43 sgo:sdDataset articles
44 rdf:type schema:ScholarlyArticle
45 N07a179c12c534c2a8bddb52598baba3d schema:name doi
46 schema:value 10.1007/s10593-011-0723-2
47 rdf:type schema:PropertyValue
48 N23e3f1ffbd904372be3d78bf29ec61cb rdf:first sg:person.01335445233.59
49 rdf:rest N7f0e7156915b4bd0a9179fffda8ae57c
50 N2c5c2ed42f3e41f1b65eb386151ae1c5 schema:name Springer Nature - SN SciGraph project
51 rdf:type schema:Organization
52 N2d8da8bc527e4757a62542e1a404d9a2 rdf:first sg:person.012501266731.37
53 rdf:rest N6a49b5d54b5a41cbbe1089e79c668700
54 N5600c22fac1e4fad84a6647b38e8d2f6 schema:volumeNumber 47
55 rdf:type schema:PublicationVolume
56 N5d247cb34b2743cdb250f70e2be8b795 schema:issueNumber 1
57 rdf:type schema:PublicationIssue
58 N609941dff205400ebb7358eb5517d456 schema:name dimensions_id
59 schema:value pub.1014350135
60 rdf:type schema:PropertyValue
61 N6a49b5d54b5a41cbbe1089e79c668700 rdf:first sg:person.010142146727.55
62 rdf:rest rdf:nil
63 N7f0e7156915b4bd0a9179fffda8ae57c rdf:first sg:person.015517326524.13
64 rdf:rest N2d8da8bc527e4757a62542e1a404d9a2
65 Naedcdab67d064cdcb5e2cc7254b62626 rdf:first sg:person.010236335635.38
66 rdf:rest N23e3f1ffbd904372be3d78bf29ec61cb
67 Ne5b276577af049b6aaf7152e0f82d15a schema:name readcube_id
68 schema:value 445cde802ff6b0c42318b5c378ce3dced3333329c01082575f8af3027b134692
69 rdf:type schema:PropertyValue
70 anzsrc-for:02 schema:inDefinedTermSet anzsrc-for:
71 schema:name Physical Sciences
72 rdf:type schema:DefinedTerm
73 anzsrc-for:0202 schema:inDefinedTermSet anzsrc-for:
74 schema:name Atomic, Molecular, Nuclear, Particle and Plasma Physics
75 rdf:type schema:DefinedTerm
76 sg:journal.1356886 schema:issn 0009-3122
77 1573-8353
78 schema:name Chemistry of Heterocyclic Compounds
79 rdf:type schema:Periodical
80 sg:person.010142146727.55 schema:affiliation https://www.grid.ac/institutes/grid.431939.5
81 schema:familyName Antipin
82 schema:givenName M. Yu.
83 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010142146727.55
84 rdf:type schema:Person
85 sg:person.010236335635.38 schema:affiliation https://www.grid.ac/institutes/grid.20567.36
86 schema:familyName Shestakov
87 schema:givenName A. S.
88 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010236335635.38
89 rdf:type schema:Person
90 sg:person.012501266731.37 schema:affiliation https://www.grid.ac/institutes/grid.20567.36
91 schema:familyName Shikhaliev
92 schema:givenName Kh. S.
93 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012501266731.37
94 rdf:type schema:Person
95 sg:person.01335445233.59 schema:affiliation https://www.grid.ac/institutes/grid.431939.5
96 schema:familyName Bushmarinov
97 schema:givenName I. S.
98 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01335445233.59
99 rdf:type schema:Person
100 sg:person.015517326524.13 schema:affiliation https://www.grid.ac/institutes/grid.20567.36
101 schema:familyName Sidorenko
102 schema:givenName O. E.
103 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015517326524.13
104 rdf:type schema:Person
105 sg:pub.10.1007/bf00486967 schema:sameAs https://app.dimensions.ai/details/publication/pub.1052115694
106 https://doi.org/10.1007/bf00486967
107 rdf:type schema:CreativeWork
108 sg:pub.10.1007/bf00512966 schema:sameAs https://app.dimensions.ai/details/publication/pub.1052690454
109 https://doi.org/10.1007/bf00512966
110 rdf:type schema:CreativeWork
111 https://doi.org/10.1002/cber.19610941207 schema:sameAs https://app.dimensions.ai/details/publication/pub.1010527679
112 rdf:type schema:CreativeWork
113 https://doi.org/10.1002/jhet.5570020106 schema:sameAs https://app.dimensions.ai/details/publication/pub.1002769892
114 rdf:type schema:CreativeWork
115 https://doi.org/10.1002/jhet.5570250119 schema:sameAs https://app.dimensions.ai/details/publication/pub.1047677478
116 rdf:type schema:CreativeWork
117 https://doi.org/10.1021/cc700143n schema:sameAs https://app.dimensions.ai/details/publication/pub.1055228269
118 rdf:type schema:CreativeWork
119 https://doi.org/10.1021/jm00316a003 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055943104
120 rdf:type schema:CreativeWork
121 https://doi.org/10.1021/jm9900321 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055959336
122 rdf:type schema:CreativeWork
123 https://doi.org/10.1021/jm990049j schema:sameAs https://app.dimensions.ai/details/publication/pub.1055959350
124 rdf:type schema:CreativeWork
125 https://doi.org/10.1021/jo00103a021 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055966752
126 rdf:type schema:CreativeWork
127 https://doi.org/10.1021/jo8008758 schema:sameAs https://app.dimensions.ai/details/publication/pub.1056032458
128 rdf:type schema:CreativeWork
129 https://doi.org/10.1021/np020050c schema:sameAs https://app.dimensions.ai/details/publication/pub.1056228561
130 rdf:type schema:CreativeWork
131 https://doi.org/10.1021/np0305223 schema:sameAs https://app.dimensions.ai/details/publication/pub.1056229275
132 rdf:type schema:CreativeWork
133 https://doi.org/10.1021/ol062421c schema:sameAs https://app.dimensions.ai/details/publication/pub.1056248634
134 rdf:type schema:CreativeWork
135 https://doi.org/10.1107/s0108767307043930 schema:sameAs https://app.dimensions.ai/details/publication/pub.1027786902
136 rdf:type schema:CreativeWork
137 https://doi.org/10.1246/bcsj.56.3703 schema:sameAs https://app.dimensions.ai/details/publication/pub.1019436657
138 rdf:type schema:CreativeWork
139 https://doi.org/10.1248/cpb.19.2284 schema:sameAs https://app.dimensions.ai/details/publication/pub.1049976355
140 rdf:type schema:CreativeWork
141 https://doi.org/10.1248/cpb.32.4666 schema:sameAs https://app.dimensions.ai/details/publication/pub.1026862237
142 rdf:type schema:CreativeWork
143 https://www.grid.ac/institutes/grid.20567.36 schema:alternateName Voronezh State University
144 schema:name Voronezh State University, Universitestskaya Pl., 1, 394006, Voronezh, Russia
145 rdf:type schema:Organization
146 https://www.grid.ac/institutes/grid.431939.5 schema:alternateName A. N. Nesmeyanov Institute of Organoelement Compounds
147 schema:name A. N. Nesmeyanov Institute of Organoelement Compounds, 28 Vavilova Str., 119991, Moscow, Russia
148 rdf:type schema:Organization
 




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


...