Glycolurils in α-ureido- and α-aminoalkylation reactions View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2008-08

AUTHORS

A. N. Kravchenko, G. A. Gazieva, N. G. Kolotyrkina, N. N. Makhova

ABSTRACT

α-Ureidoalkylation of 1,3- and 1,1-dimethylureas with 2-(hydroxymethyl)-, 2,6- and 2,8-di(hydroxymethyl)-, and 2,4,6,8-tetra(hydroxymethyl)glycolurils gave novel bi-, tri-, tetra-, and pentacyclic fused systems combining the glycoluril and urea fragments.

PAGES

1760-1764

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-008-0233-2

DOI

http://dx.doi.org/10.1007/s11172-008-0233-2

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1031318817


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/2008/03", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Chemical Sciences", 
        "type": "DefinedTerm"
      }, 
      {
        "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"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.439283.7", 
          "name": [
            "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Kravchenko", 
        "givenName": "A. N.", 
        "id": "sg:person.016427042461.48", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016427042461.48"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.439283.7", 
          "name": [
            "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Gazieva", 
        "givenName": "G. A.", 
        "id": "sg:person.010204472230.49", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010204472230.49"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.439283.7", 
          "name": [
            "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Kolotyrkina", 
        "givenName": "N. G.", 
        "id": "sg:person.016374705303.78", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016374705303.78"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation", 
          "id": "http://www.grid.ac/institutes/grid.439283.7", 
          "name": [
            "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Makhova", 
        "givenName": "N. N.", 
        "id": "sg:person.016546763131.27", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016546763131.27"
        ], 
        "type": "Person"
      }
    ], 
    "datePublished": "2008-08", 
    "datePublishedReg": "2008-08-01", 
    "description": "Abstract\u03b1-Ureidoalkylation of 1,3- and 1,1-dimethylureas with 2-(hydroxymethyl)-, 2,6- and 2,8-di(hydroxymethyl)-, and 2,4,6,8-tetra(hydroxymethyl)glycolurils gave novel bi-, tri-, tetra-, and pentacyclic fused systems combining the glycoluril and urea fragments.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/s11172-008-0233-2", 
    "inLanguage": "en", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1022309", 
        "issn": [
          "1063-5211", 
          "1026-3500"
        ], 
        "name": "Russian Chemical Bulletin", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "8", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "57"
      }
    ], 
    "keywords": [
      "fragments", 
      "reaction", 
      "novel bis", 
      "system", 
      "urea fragment", 
      "ureido", 
      "aminoalkylation reaction", 
      "Bi", 
      "tri", 
      "tetra", 
      "glycoluril", 
      "Abstract\u03b1-Ureidoalkylation"
    ], 
    "name": "Glycolurils in \u03b1-ureido- and \u03b1-aminoalkylation reactions", 
    "pagination": "1760-1764", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1031318817"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s11172-008-0233-2"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s11172-008-0233-2", 
      "https://app.dimensions.ai/details/publication/pub.1031318817"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2021-12-01T19:21", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20211201/entities/gbq_results/article/article_469.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/s11172-008-0233-2"
  }
]
 

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/s11172-008-0233-2'

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/s11172-008-0233-2'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s11172-008-0233-2'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s11172-008-0233-2'


 

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

91 TRIPLES      21 PREDICATES      38 URIs      30 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s11172-008-0233-2 schema:about anzsrc-for:03
2 anzsrc-for:0306
3 schema:author N536b248173294969a3e58b68db3ef281
4 schema:datePublished 2008-08
5 schema:datePublishedReg 2008-08-01
6 schema:description Abstractα-Ureidoalkylation of 1,3- and 1,1-dimethylureas with 2-(hydroxymethyl)-, 2,6- and 2,8-di(hydroxymethyl)-, and 2,4,6,8-tetra(hydroxymethyl)glycolurils gave novel bi-, tri-, tetra-, and pentacyclic fused systems combining the glycoluril and urea fragments.
7 schema:genre article
8 schema:inLanguage en
9 schema:isAccessibleForFree false
10 schema:isPartOf N45d9d2b061294954a31b746aff850725
11 N65ec99762dc647acb46fcb257825233e
12 sg:journal.1022309
13 schema:keywords Abstractα-Ureidoalkylation
14 Bi
15 aminoalkylation reaction
16 fragments
17 glycoluril
18 novel bis
19 reaction
20 system
21 tetra
22 tri
23 urea fragment
24 ureido
25 schema:name Glycolurils in α-ureido- and α-aminoalkylation reactions
26 schema:pagination 1760-1764
27 schema:productId N0bbfadaee41f4357a1fe80033cbd9588
28 Ne039fa06943c4ed8821bb198300d5c30
29 schema:sameAs https://app.dimensions.ai/details/publication/pub.1031318817
30 https://doi.org/10.1007/s11172-008-0233-2
31 schema:sdDatePublished 2021-12-01T19:21
32 schema:sdLicense https://scigraph.springernature.com/explorer/license/
33 schema:sdPublisher Nfd95b461e90d4c989abf2c52b99e1051
34 schema:url https://doi.org/10.1007/s11172-008-0233-2
35 sgo:license sg:explorer/license/
36 sgo:sdDataset articles
37 rdf:type schema:ScholarlyArticle
38 N0bbfadaee41f4357a1fe80033cbd9588 schema:name doi
39 schema:value 10.1007/s11172-008-0233-2
40 rdf:type schema:PropertyValue
41 N10f49f24ae824751a6818164660da8fc rdf:first sg:person.016546763131.27
42 rdf:rest rdf:nil
43 N1dd0247c63de4bd6a2f2b731b18138f5 rdf:first sg:person.016374705303.78
44 rdf:rest N10f49f24ae824751a6818164660da8fc
45 N45d9d2b061294954a31b746aff850725 schema:issueNumber 8
46 rdf:type schema:PublicationIssue
47 N536b248173294969a3e58b68db3ef281 rdf:first sg:person.016427042461.48
48 rdf:rest N7b1cd2ae97fc44bd86b2e382933def34
49 N65ec99762dc647acb46fcb257825233e schema:volumeNumber 57
50 rdf:type schema:PublicationVolume
51 N7b1cd2ae97fc44bd86b2e382933def34 rdf:first sg:person.010204472230.49
52 rdf:rest N1dd0247c63de4bd6a2f2b731b18138f5
53 Ne039fa06943c4ed8821bb198300d5c30 schema:name dimensions_id
54 schema:value pub.1031318817
55 rdf:type schema:PropertyValue
56 Nfd95b461e90d4c989abf2c52b99e1051 schema:name Springer Nature - SN SciGraph project
57 rdf:type schema:Organization
58 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
59 schema:name Chemical Sciences
60 rdf:type schema:DefinedTerm
61 anzsrc-for:0306 schema:inDefinedTermSet anzsrc-for:
62 schema:name Physical Chemistry (incl. Structural)
63 rdf:type schema:DefinedTerm
64 sg:journal.1022309 schema:issn 1026-3500
65 1063-5211
66 schema:name Russian Chemical Bulletin
67 schema:publisher Springer Nature
68 rdf:type schema:Periodical
69 sg:person.010204472230.49 schema:affiliation grid-institutes:grid.439283.7
70 schema:familyName Gazieva
71 schema:givenName G. A.
72 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010204472230.49
73 rdf:type schema:Person
74 sg:person.016374705303.78 schema:affiliation grid-institutes:grid.439283.7
75 schema:familyName Kolotyrkina
76 schema:givenName N. G.
77 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016374705303.78
78 rdf:type schema:Person
79 sg:person.016427042461.48 schema:affiliation grid-institutes:grid.439283.7
80 schema:familyName Kravchenko
81 schema:givenName A. N.
82 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016427042461.48
83 rdf:type schema:Person
84 sg:person.016546763131.27 schema:affiliation grid-institutes:grid.439283.7
85 schema:familyName Makhova
86 schema:givenName N. N.
87 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016546763131.27
88 rdf:type schema:Person
89 grid-institutes:grid.439283.7 schema:alternateName N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation
90 schema:name N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation
91 rdf:type schema:Organization
 




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


...