Glycoconjugates of amines: alkylation of primary and secondary amines withN-chloroacetyl-β-glycopyranosylamines View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1998-06

AUTHORS

L. M. Likhosherstov, O. S. Novikova, V. N. Shibaev

ABSTRACT

Efficient monoalkylation of a series of primary and secondary amines was demonstrated with the use ofN-chloroacetylglycosylamines derived fromd-glucose,d-galactose,d-mannose,N-acetyl-d-glucosamine, and lactose. The reaction was shown to be useful for incorporation of carbohydrate residues into physiologically active compounds. Glycoconjugates of some derivatives of piperazine, 2-phenylethylamine, tryptamine, and important biogenic amines (norephedrine, octopamine, dopamine) were prepared. More... »

PAGES

1214-1217

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf02503499

DOI

http://dx.doi.org/10.1007/bf02503499

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1003895526


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/2008/0303", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Macromolecular and Materials Chemistry", 
        "type": "DefinedTerm"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 117913, 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., 117913, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Likhosherstov", 
        "givenName": "L. M.", 
        "id": "sg:person.01222113333.75", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01222113333.75"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 117913, 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., 117913, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Novikova", 
        "givenName": "O. S.", 
        "id": "sg:person.0641301571.82", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0641301571.82"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 117913, 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., 117913, Moscow, Russian Federation"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Shibaev", 
        "givenName": "V. N.", 
        "id": "sg:person.015075554137.34", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015075554137.34"
        ], 
        "type": "Person"
      }
    ], 
    "datePublished": "1998-06", 
    "datePublishedReg": "1998-06-01", 
    "description": "Efficient monoalkylation of a series of primary and secondary amines was demonstrated with the use ofN-chloroacetylglycosylamines derived fromd-glucose,d-galactose,d-mannose,N-acetyl-d-glucosamine, and lactose. The reaction was shown to be useful for incorporation of carbohydrate residues into physiologically active compounds. Glycoconjugates of some derivatives of piperazine, 2-phenylethylamine, tryptamine, and important biogenic amines (norephedrine, octopamine, dopamine) were prepared.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/bf02503499", 
    "inLanguage": "en", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1022309", 
        "issn": [
          "1026-3500", 
          "1066-5285"
        ], 
        "name": "Russian Chemical Bulletin", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "6", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "47"
      }
    ], 
    "keywords": [
      "derivatives of piperazine", 
      "secondary amines", 
      "active compounds", 
      "important biogenic amines", 
      "amines", 
      "carbohydrate residues", 
      "glycopyranosylamines", 
      "monoalkylation", 
      "alkylation", 
      "piperazine", 
      "compounds", 
      "derivatives", 
      "reaction", 
      "glycoconjugates", 
      "biogenic amines", 
      "tryptamine", 
      "incorporation", 
      "mannose", 
      "acetyl", 
      "residues", 
      "glucosamine", 
      "galactose", 
      "series", 
      "use"
    ], 
    "name": "Glycoconjugates of amines: alkylation of primary and secondary amines withN-chloroacetyl-\u03b2-glycopyranosylamines", 
    "pagination": "1214-1217", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1003895526"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/bf02503499"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/bf02503499", 
      "https://app.dimensions.ai/details/publication/pub.1003895526"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2022-05-20T07:20", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20220519/entities/gbq_results/article/article_271.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/bf02503499"
  }
]
 

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/bf02503499'

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/bf02503499'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf02503499'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf02503499'


 

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

96 TRIPLES      21 PREDICATES      50 URIs      42 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/bf02503499 schema:about anzsrc-for:03
2 anzsrc-for:0303
3 schema:author Nd77a9e7a1d9d4b0095ea6c562c964746
4 schema:datePublished 1998-06
5 schema:datePublishedReg 1998-06-01
6 schema:description Efficient monoalkylation of a series of primary and secondary amines was demonstrated with the use ofN-chloroacetylglycosylamines derived fromd-glucose,d-galactose,d-mannose,N-acetyl-d-glucosamine, and lactose. The reaction was shown to be useful for incorporation of carbohydrate residues into physiologically active compounds. Glycoconjugates of some derivatives of piperazine, 2-phenylethylamine, tryptamine, and important biogenic amines (norephedrine, octopamine, dopamine) were prepared.
7 schema:genre article
8 schema:inLanguage en
9 schema:isAccessibleForFree false
10 schema:isPartOf N0cbc683cb86d4d479cbfacd6d585b2e3
11 Na7c1d5514b444d6a83f2c4a9db1ec46a
12 sg:journal.1022309
13 schema:keywords acetyl
14 active compounds
15 alkylation
16 amines
17 biogenic amines
18 carbohydrate residues
19 compounds
20 derivatives
21 derivatives of piperazine
22 galactose
23 glucosamine
24 glycoconjugates
25 glycopyranosylamines
26 important biogenic amines
27 incorporation
28 mannose
29 monoalkylation
30 piperazine
31 reaction
32 residues
33 secondary amines
34 series
35 tryptamine
36 use
37 schema:name Glycoconjugates of amines: alkylation of primary and secondary amines withN-chloroacetyl-β-glycopyranosylamines
38 schema:pagination 1214-1217
39 schema:productId N91ea92afb36444c281611d7b083b72d6
40 N9435b6f99a6349deb3f2afb9fef187fe
41 schema:sameAs https://app.dimensions.ai/details/publication/pub.1003895526
42 https://doi.org/10.1007/bf02503499
43 schema:sdDatePublished 2022-05-20T07:20
44 schema:sdLicense https://scigraph.springernature.com/explorer/license/
45 schema:sdPublisher N8d498e6dd4cf4001a270444007bb92bb
46 schema:url https://doi.org/10.1007/bf02503499
47 sgo:license sg:explorer/license/
48 sgo:sdDataset articles
49 rdf:type schema:ScholarlyArticle
50 N0cbc683cb86d4d479cbfacd6d585b2e3 schema:issueNumber 6
51 rdf:type schema:PublicationIssue
52 N301ed1de31b34dfca2e7a75b893e2541 rdf:first sg:person.0641301571.82
53 rdf:rest Naf9c83ce20cc44c1ac7897f66da3af07
54 N8d498e6dd4cf4001a270444007bb92bb schema:name Springer Nature - SN SciGraph project
55 rdf:type schema:Organization
56 N91ea92afb36444c281611d7b083b72d6 schema:name dimensions_id
57 schema:value pub.1003895526
58 rdf:type schema:PropertyValue
59 N9435b6f99a6349deb3f2afb9fef187fe schema:name doi
60 schema:value 10.1007/bf02503499
61 rdf:type schema:PropertyValue
62 Na7c1d5514b444d6a83f2c4a9db1ec46a schema:volumeNumber 47
63 rdf:type schema:PublicationVolume
64 Naf9c83ce20cc44c1ac7897f66da3af07 rdf:first sg:person.015075554137.34
65 rdf:rest rdf:nil
66 Nd77a9e7a1d9d4b0095ea6c562c964746 rdf:first sg:person.01222113333.75
67 rdf:rest N301ed1de31b34dfca2e7a75b893e2541
68 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
69 schema:name Chemical Sciences
70 rdf:type schema:DefinedTerm
71 anzsrc-for:0303 schema:inDefinedTermSet anzsrc-for:
72 schema:name Macromolecular and Materials Chemistry
73 rdf:type schema:DefinedTerm
74 sg:journal.1022309 schema:issn 1026-3500
75 1066-5285
76 schema:name Russian Chemical Bulletin
77 schema:publisher Springer Nature
78 rdf:type schema:Periodical
79 sg:person.01222113333.75 schema:affiliation grid-institutes:grid.439283.7
80 schema:familyName Likhosherstov
81 schema:givenName L. M.
82 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01222113333.75
83 rdf:type schema:Person
84 sg:person.015075554137.34 schema:affiliation grid-institutes:grid.439283.7
85 schema:familyName Shibaev
86 schema:givenName V. N.
87 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015075554137.34
88 rdf:type schema:Person
89 sg:person.0641301571.82 schema:affiliation grid-institutes:grid.439283.7
90 schema:familyName Novikova
91 schema:givenName O. S.
92 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0641301571.82
93 rdf:type schema:Person
94 grid-institutes:grid.439283.7 schema:alternateName N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 117913, Moscow, Russian Federation
95 schema:name N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 117913, Moscow, Russian Federation
96 rdf:type schema:Organization
 




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


...