Synthesis of a new hetrocyclic system 7,8-dihydroimidazo[1,2-c][1,3]oxazolo[4,5-e]pyrimidine View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2010-12-04

AUTHORS

A. P. Kozachenko, O. V. Shablykin, A. N. Chernega, V. S. Brovarets

ABSTRACT

2-(Acylaminocyanomethylene)imidazolidines are formed on interacting 2-acylamino-3,3-dichloro-acrylonitriles with ethylenediamine. The former are converted into new derivatives of oxazolo-[4,5-e]pyrimidine on treatment with trifluoroacetic acid, and then with triethyl orthoformate.

PAGES

1116-1121

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-010-0635-6

DOI

http://dx.doi.org/10.1007/s10593-010-0635-6

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1050166170


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/2008/0305", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Organic Chemistry", 
        "type": "DefinedTerm"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 02660, Kiev, Ukraine", 
          "id": "http://www.grid.ac/institutes/grid.424920.9", 
          "name": [
            "Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 02660, Kiev, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Kozachenko", 
        "givenName": "A. P.", 
        "id": "sg:person.010162050171.14", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010162050171.14"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 02660, Kiev, Ukraine", 
          "id": "http://www.grid.ac/institutes/grid.424920.9", 
          "name": [
            "Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 02660, Kiev, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Shablykin", 
        "givenName": "O. V.", 
        "id": "sg:person.01120365303.86", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01120365303.86"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Organic Chemistry, National Academy of Sciences of Ukraine, 02094, Kiev, Ukraine", 
          "id": "http://www.grid.ac/institutes/grid.464621.3", 
          "name": [
            "Institute of Organic Chemistry, National Academy of Sciences of Ukraine, 02094, Kiev, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Chernega", 
        "givenName": "A. N.", 
        "id": "sg:person.011763241323.49", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011763241323.49"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 02660, Kiev, Ukraine", 
          "id": "http://www.grid.ac/institutes/grid.424920.9", 
          "name": [
            "Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 02660, Kiev, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Brovarets", 
        "givenName": "V. S.", 
        "id": "sg:person.010072133553.61", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010072133553.61"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "sg:pub.10.1007/s00706-006-0519-8", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1010805746", 
          "https://doi.org/10.1007/s00706-006-0519-8"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2010-12-04", 
    "datePublishedReg": "2010-12-04", 
    "description": "2-(Acylaminocyanomethylene)imidazolidines are formed on interacting 2-acylamino-3,3-dichloro-acrylonitriles with ethylenediamine. The former are converted into new derivatives of oxazolo-[4,5-e]pyrimidine on treatment with trifluoroacetic acid, and then with triethyl orthoformate.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/s10593-010-0635-6", 
    "inLanguage": "en", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1358699", 
        "issn": [
          "0132-6244", 
          "1573-8353"
        ], 
        "name": "Chemistry of Heterocyclic Compounds", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "9", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "46"
      }
    ], 
    "keywords": [
      "treatment", 
      "new derivatives", 
      "acid", 
      "derivatives", 
      "synthesis", 
      "system", 
      "trifluoroacetic acid", 
      "acrylonitrile", 
      "ethylenediamine", 
      "triethyl", 
      "new hetrocyclic system", 
      "hetrocyclic system"
    ], 
    "name": "Synthesis of a new hetrocyclic system 7,8-dihydroimidazo[1,2-c][1,3]oxazolo[4,5-e]pyrimidine", 
    "pagination": "1116-1121", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1050166170"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s10593-010-0635-6"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s10593-010-0635-6", 
      "https://app.dimensions.ai/details/publication/pub.1050166170"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2021-11-01T18:15", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20211101/entities/gbq_results/article/article_515.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/s10593-010-0635-6"
  }
]
 

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/s10593-010-0635-6'

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/s10593-010-0635-6'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s10593-010-0635-6'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s10593-010-0635-6'


 

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

98 TRIPLES      22 PREDICATES      38 URIs      29 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s10593-010-0635-6 schema:about anzsrc-for:03
2 anzsrc-for:0305
3 schema:author Neba2e44a023843cfad9f1dda25108c84
4 schema:citation sg:pub.10.1007/s00706-006-0519-8
5 schema:datePublished 2010-12-04
6 schema:datePublishedReg 2010-12-04
7 schema:description 2-(Acylaminocyanomethylene)imidazolidines are formed on interacting 2-acylamino-3,3-dichloro-acrylonitriles with ethylenediamine. The former are converted into new derivatives of oxazolo-[4,5-e]pyrimidine on treatment with trifluoroacetic acid, and then with triethyl orthoformate.
8 schema:genre article
9 schema:inLanguage en
10 schema:isAccessibleForFree false
11 schema:isPartOf N56e74c2cd9e447b8b34a2b59173493c9
12 Nabaa66ed0bc249fd891af1950d62223d
13 sg:journal.1358699
14 schema:keywords acid
15 acrylonitrile
16 derivatives
17 ethylenediamine
18 hetrocyclic system
19 new derivatives
20 new hetrocyclic system
21 synthesis
22 system
23 treatment
24 triethyl
25 trifluoroacetic acid
26 schema:name Synthesis of a new hetrocyclic system 7,8-dihydroimidazo[1,2-c][1,3]oxazolo[4,5-e]pyrimidine
27 schema:pagination 1116-1121
28 schema:productId N1812d36c356c4f60bbba8a7bbffee437
29 Nf283ce337ee34213be740c59fa62fd5f
30 schema:sameAs https://app.dimensions.ai/details/publication/pub.1050166170
31 https://doi.org/10.1007/s10593-010-0635-6
32 schema:sdDatePublished 2021-11-01T18:15
33 schema:sdLicense https://scigraph.springernature.com/explorer/license/
34 schema:sdPublisher Nf94e8bb77d1347f9941e2b89594e5fe1
35 schema:url https://doi.org/10.1007/s10593-010-0635-6
36 sgo:license sg:explorer/license/
37 sgo:sdDataset articles
38 rdf:type schema:ScholarlyArticle
39 N1812d36c356c4f60bbba8a7bbffee437 schema:name doi
40 schema:value 10.1007/s10593-010-0635-6
41 rdf:type schema:PropertyValue
42 N56e74c2cd9e447b8b34a2b59173493c9 schema:volumeNumber 46
43 rdf:type schema:PublicationVolume
44 Nabaa66ed0bc249fd891af1950d62223d schema:issueNumber 9
45 rdf:type schema:PublicationIssue
46 Nae0340cab97144b8a4d8b8d85fd2dc15 rdf:first sg:person.01120365303.86
47 rdf:rest Nfbeaf824395f4d64908556b60540c56f
48 Nc5cbef8e8d134c959b41c820093399d0 rdf:first sg:person.010072133553.61
49 rdf:rest rdf:nil
50 Neba2e44a023843cfad9f1dda25108c84 rdf:first sg:person.010162050171.14
51 rdf:rest Nae0340cab97144b8a4d8b8d85fd2dc15
52 Nf283ce337ee34213be740c59fa62fd5f schema:name dimensions_id
53 schema:value pub.1050166170
54 rdf:type schema:PropertyValue
55 Nf94e8bb77d1347f9941e2b89594e5fe1 schema:name Springer Nature - SN SciGraph project
56 rdf:type schema:Organization
57 Nfbeaf824395f4d64908556b60540c56f rdf:first sg:person.011763241323.49
58 rdf:rest Nc5cbef8e8d134c959b41c820093399d0
59 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
60 schema:name Chemical Sciences
61 rdf:type schema:DefinedTerm
62 anzsrc-for:0305 schema:inDefinedTermSet anzsrc-for:
63 schema:name Organic Chemistry
64 rdf:type schema:DefinedTerm
65 sg:journal.1358699 schema:issn 0132-6244
66 1573-8353
67 schema:name Chemistry of Heterocyclic Compounds
68 schema:publisher Springer Nature
69 rdf:type schema:Periodical
70 sg:person.010072133553.61 schema:affiliation grid-institutes:grid.424920.9
71 schema:familyName Brovarets
72 schema:givenName V. S.
73 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010072133553.61
74 rdf:type schema:Person
75 sg:person.010162050171.14 schema:affiliation grid-institutes:grid.424920.9
76 schema:familyName Kozachenko
77 schema:givenName A. P.
78 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010162050171.14
79 rdf:type schema:Person
80 sg:person.01120365303.86 schema:affiliation grid-institutes:grid.424920.9
81 schema:familyName Shablykin
82 schema:givenName O. V.
83 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01120365303.86
84 rdf:type schema:Person
85 sg:person.011763241323.49 schema:affiliation grid-institutes:grid.464621.3
86 schema:familyName Chernega
87 schema:givenName A. N.
88 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011763241323.49
89 rdf:type schema:Person
90 sg:pub.10.1007/s00706-006-0519-8 schema:sameAs https://app.dimensions.ai/details/publication/pub.1010805746
91 https://doi.org/10.1007/s00706-006-0519-8
92 rdf:type schema:CreativeWork
93 grid-institutes:grid.424920.9 schema:alternateName Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 02660, Kiev, Ukraine
94 schema:name Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, 02660, Kiev, Ukraine
95 rdf:type schema:Organization
96 grid-institutes:grid.464621.3 schema:alternateName Institute of Organic Chemistry, National Academy of Sciences of Ukraine, 02094, Kiev, Ukraine
97 schema:name Institute of Organic Chemistry, National Academy of Sciences of Ukraine, 02094, Kiev, Ukraine
98 rdf:type schema:Organization
 




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


...