Derivatives of 1,1,2,2-tetraaminoethane: II. Condensation of 4,5-diacetoxy-1,3-diacetylimidazolidine and 2,3-diacetoxy-1,4-diacetylpiperazine with nitrogen-containing nucleophiles View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2007-04

AUTHORS

E. V. Sizova, V. V. Sizov, I. V. Tselinskii

ABSTRACT

Reactions of 4,5-diacetoxy-1,3-diacetylimidazolidine and 2,3-diacetoxy-1,4-diacetylpiperazine with acetamide and ethyl carbamate gave 1,3-diacetyl-4,5-bis(acetylamino)imidazolidine, 1,4-diacetyl-2,3-bis(acetylamino)piperazine, 1,3-diacetyl-4,5-bis(ethoxycarbonylamino)imidazolidine, and 1,4-diacetyl-2,3-bis(ethoxycarbonylamino)piperazine, respectively. Condensation products of 4,5-diacetoxy-1,3-diacetylimidazolidine and 2,3-diacetoxy-1,4-diacetylpiperazine with urea, furazan-3,4-diamine, and 4-phenylfurazan-3-amine were isolated.

PAGES

596-601

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070428007040185

DOI

http://dx.doi.org/10.1134/s1070428007040185

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1013108847


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/2008/0399", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Other Chemical Sciences", 
        "type": "DefinedTerm"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "St. Petersburg State Institute of Technology, Moskovskii pr. 26, 190013, St. Petersburg, Russia", 
          "id": "http://www.grid.ac/institutes/grid.437869.7", 
          "name": [
            "St. Petersburg State Institute of Technology, Moskovskii pr. 26, 190013, St. Petersburg, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Sizova", 
        "givenName": "E. V.", 
        "id": "sg:person.011023662675.38", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011023662675.38"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "St. Petersburg State Institute of Technology, Moskovskii pr. 26, 190013, St. Petersburg, Russia", 
          "id": "http://www.grid.ac/institutes/grid.437869.7", 
          "name": [
            "St. Petersburg State Institute of Technology, Moskovskii pr. 26, 190013, St. Petersburg, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Sizov", 
        "givenName": "V. V.", 
        "id": "sg:person.014433331415.77", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014433331415.77"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "St. Petersburg State Institute of Technology, Moskovskii pr. 26, 190013, St. Petersburg, Russia", 
          "id": "http://www.grid.ac/institutes/grid.437869.7", 
          "name": [
            "St. Petersburg State Institute of Technology, Moskovskii pr. 26, 190013, St. Petersburg, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Tselinskii", 
        "givenName": "I. V.", 
        "id": "sg:person.015404525675.24", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015404525675.24"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "sg:pub.10.1134/s1070428007020029", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1008457844", 
          "https://doi.org/10.1134/s1070428007020029"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2007-04", 
    "datePublishedReg": "2007-04-01", 
    "description": "Reactions of 4,5-diacetoxy-1,3-diacetylimidazolidine and 2,3-diacetoxy-1,4-diacetylpiperazine with acetamide and ethyl carbamate gave 1,3-diacetyl-4,5-bis(acetylamino)imidazolidine, 1,4-diacetyl-2,3-bis(acetylamino)piperazine, 1,3-diacetyl-4,5-bis(ethoxycarbonylamino)imidazolidine, and 1,4-diacetyl-2,3-bis(ethoxycarbonylamino)piperazine, respectively. Condensation products of 4,5-diacetoxy-1,3-diacetylimidazolidine and 2,3-diacetoxy-1,4-diacetylpiperazine with urea, furazan-3,4-diamine, and 4-phenylfurazan-3-amine were isolated.", 
    "genre": "article", 
    "id": "sg:pub.10.1134/s1070428007040185", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1136317", 
        "issn": [
          "1070-4280", 
          "1608-3393"
        ], 
        "name": "Russian Journal of Organic Chemistry", 
        "publisher": "Pleiades Publishing", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "4", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "43"
      }
    ], 
    "keywords": [
      "nitrogen-containing nucleophiles", 
      "condensation products", 
      "diacetylpiperazine", 
      "diacetoxy", 
      "diacetyl", 
      "ethyl carbamate", 
      "diamine", 
      "nucleophiles", 
      "acetamide", 
      "carbamate", 
      "reaction", 
      "derivatives", 
      "condensation", 
      "products"
    ], 
    "name": "Derivatives of 1,1,2,2-tetraaminoethane: II. Condensation of 4,5-diacetoxy-1,3-diacetylimidazolidine and 2,3-diacetoxy-1,4-diacetylpiperazine with nitrogen-containing nucleophiles", 
    "pagination": "596-601", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1013108847"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1134/s1070428007040185"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1134/s1070428007040185", 
      "https://app.dimensions.ai/details/publication/pub.1013108847"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-12-01T06:26", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20221201/entities/gbq_results/article/article_444.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1134/s1070428007040185"
  }
]
 

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/s1070428007040185'

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/s1070428007040185'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1134/s1070428007040185'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1134/s1070428007040185'


 

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

89 TRIPLES      21 PREDICATES      40 URIs      31 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1134/s1070428007040185 schema:about anzsrc-for:03
2 anzsrc-for:0399
3 schema:author N4c76a63b702c4b8189eb4965b218745b
4 schema:citation sg:pub.10.1134/s1070428007020029
5 schema:datePublished 2007-04
6 schema:datePublishedReg 2007-04-01
7 schema:description Reactions of 4,5-diacetoxy-1,3-diacetylimidazolidine and 2,3-diacetoxy-1,4-diacetylpiperazine with acetamide and ethyl carbamate gave 1,3-diacetyl-4,5-bis(acetylamino)imidazolidine, 1,4-diacetyl-2,3-bis(acetylamino)piperazine, 1,3-diacetyl-4,5-bis(ethoxycarbonylamino)imidazolidine, and 1,4-diacetyl-2,3-bis(ethoxycarbonylamino)piperazine, respectively. Condensation products of 4,5-diacetoxy-1,3-diacetylimidazolidine and 2,3-diacetoxy-1,4-diacetylpiperazine with urea, furazan-3,4-diamine, and 4-phenylfurazan-3-amine were isolated.
8 schema:genre article
9 schema:isAccessibleForFree false
10 schema:isPartOf N7a616fdf1c094c27ab8c33bdd66789cb
11 Nd0dac7159f3c40ba888d4b8fd122c9fc
12 sg:journal.1136317
13 schema:keywords acetamide
14 carbamate
15 condensation
16 condensation products
17 derivatives
18 diacetoxy
19 diacetyl
20 diacetylpiperazine
21 diamine
22 ethyl carbamate
23 nitrogen-containing nucleophiles
24 nucleophiles
25 products
26 reaction
27 schema:name Derivatives of 1,1,2,2-tetraaminoethane: II. Condensation of 4,5-diacetoxy-1,3-diacetylimidazolidine and 2,3-diacetoxy-1,4-diacetylpiperazine with nitrogen-containing nucleophiles
28 schema:pagination 596-601
29 schema:productId N82a5b5c07561414d9b21da8f7b44affa
30 Nb548d5fa1cc9439987b4843fe2a1b530
31 schema:sameAs https://app.dimensions.ai/details/publication/pub.1013108847
32 https://doi.org/10.1134/s1070428007040185
33 schema:sdDatePublished 2022-12-01T06:26
34 schema:sdLicense https://scigraph.springernature.com/explorer/license/
35 schema:sdPublisher N3818c159665149bf81a1dab9d2e63738
36 schema:url https://doi.org/10.1134/s1070428007040185
37 sgo:license sg:explorer/license/
38 sgo:sdDataset articles
39 rdf:type schema:ScholarlyArticle
40 N3818c159665149bf81a1dab9d2e63738 schema:name Springer Nature - SN SciGraph project
41 rdf:type schema:Organization
42 N4c76a63b702c4b8189eb4965b218745b rdf:first sg:person.011023662675.38
43 rdf:rest N637ef5032b734c9fbb13e51f89cc2d9b
44 N4cbab97821174147a1950baf69b6aa3d rdf:first sg:person.015404525675.24
45 rdf:rest rdf:nil
46 N637ef5032b734c9fbb13e51f89cc2d9b rdf:first sg:person.014433331415.77
47 rdf:rest N4cbab97821174147a1950baf69b6aa3d
48 N7a616fdf1c094c27ab8c33bdd66789cb schema:volumeNumber 43
49 rdf:type schema:PublicationVolume
50 N82a5b5c07561414d9b21da8f7b44affa schema:name doi
51 schema:value 10.1134/s1070428007040185
52 rdf:type schema:PropertyValue
53 Nb548d5fa1cc9439987b4843fe2a1b530 schema:name dimensions_id
54 schema:value pub.1013108847
55 rdf:type schema:PropertyValue
56 Nd0dac7159f3c40ba888d4b8fd122c9fc schema:issueNumber 4
57 rdf:type schema:PublicationIssue
58 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
59 schema:name Chemical Sciences
60 rdf:type schema:DefinedTerm
61 anzsrc-for:0399 schema:inDefinedTermSet anzsrc-for:
62 schema:name Other Chemical Sciences
63 rdf:type schema:DefinedTerm
64 sg:journal.1136317 schema:issn 1070-4280
65 1608-3393
66 schema:name Russian Journal of Organic Chemistry
67 schema:publisher Pleiades Publishing
68 rdf:type schema:Periodical
69 sg:person.011023662675.38 schema:affiliation grid-institutes:grid.437869.7
70 schema:familyName Sizova
71 schema:givenName E. V.
72 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011023662675.38
73 rdf:type schema:Person
74 sg:person.014433331415.77 schema:affiliation grid-institutes:grid.437869.7
75 schema:familyName Sizov
76 schema:givenName V. V.
77 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014433331415.77
78 rdf:type schema:Person
79 sg:person.015404525675.24 schema:affiliation grid-institutes:grid.437869.7
80 schema:familyName Tselinskii
81 schema:givenName I. V.
82 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015404525675.24
83 rdf:type schema:Person
84 sg:pub.10.1134/s1070428007020029 schema:sameAs https://app.dimensions.ai/details/publication/pub.1008457844
85 https://doi.org/10.1134/s1070428007020029
86 rdf:type schema:CreativeWork
87 grid-institutes:grid.437869.7 schema:alternateName St. Petersburg State Institute of Technology, Moskovskii pr. 26, 190013, St. Petersburg, Russia
88 schema:name St. Petersburg State Institute of Technology, Moskovskii pr. 26, 190013, St. Petersburg, Russia
89 rdf:type schema:Organization
 




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


...