Lithiation of deoxypeganine and chiral synthesis of deoxypeganine derivatives View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2011-01

AUTHORS

Kh. M. Shakhidoyatov, I. Coldham, T. F. Ibragimov

ABSTRACT

A method was developed for lithiation of deoxypeganine. The reaction of organolithium deoxypeganine derivatives with isobutyraldehyde and benzaldehyde to produce its derivatives was studied. A chiral synthesis of substituted deoxypeganines was performed. The synthesized diastereomers and enantiomers were separated successfully using HPLC and a chiral column.

PAGES

929-931

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10600-011-9785-8

DOI

http://dx.doi.org/10.1007/s10600-011-9785-8

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1048769943


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/2008/0305", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Organic Chemistry", 
        "type": "DefinedTerm"
      }, 
      {
        "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"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "Academy of Sciences Republic of Uzbekistan", 
          "id": "https://www.grid.ac/institutes/grid.419209.7", 
          "name": [
            "S. Yu. Yunusov Institute of the Chemistry of Plant Substances, Academy of Sciences of the Republic of Uzbekistan, Tashkent, Uzbekistan"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Shakhidoyatov", 
        "givenName": "Kh. M.", 
        "id": "sg:person.015706066705.62", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015706066705.62"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "University of Sheffield", 
          "id": "https://www.grid.ac/institutes/grid.11835.3e", 
          "name": [
            "Department of Chemistry, University of Sheffield, Brook Hill, S3 7HF, Sheffield, UK"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Coldham", 
        "givenName": "I.", 
        "id": "sg:person.01125653241.38", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01125653241.38"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Academy of Sciences Republic of Uzbekistan", 
          "id": "https://www.grid.ac/institutes/grid.419209.7", 
          "name": [
            "S. Yu. Yunusov Institute of the Chemistry of Plant Substances, Academy of Sciences of the Republic of Uzbekistan, Tashkent, Uzbekistan"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Ibragimov", 
        "givenName": "T. F.", 
        "id": "sg:person.010304611115.11", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010304611115.11"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "https://doi.org/10.1055/s-2006-957604", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1057470628"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2011-01", 
    "datePublishedReg": "2011-01-01", 
    "description": "A method was developed for lithiation of deoxypeganine. The reaction of organolithium deoxypeganine derivatives with isobutyraldehyde and benzaldehyde to produce its derivatives was studied. A chiral synthesis of substituted deoxypeganines was performed. The synthesized diastereomers and enantiomers were separated successfully using HPLC and a chiral column.", 
    "genre": "non_research_article", 
    "id": "sg:pub.10.1007/s10600-011-9785-8", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1009660", 
        "issn": [
          "0009-3130", 
          "1573-8388"
        ], 
        "name": "Chemistry of Natural Compounds", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "6", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "46"
      }
    ], 
    "name": "Lithiation of deoxypeganine and chiral synthesis of deoxypeganine derivatives", 
    "pagination": "929-931", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "e854a408ba295239346696145a9617270d8372f8b9324bbe6eef78a3394eff9e"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s10600-011-9785-8"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1048769943"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s10600-011-9785-8", 
      "https://app.dimensions.ai/details/publication/pub.1048769943"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-10T17:33", 
    "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_8672_00000516.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "http://link.springer.com/10.1007%2Fs10600-011-9785-8"
  }
]
 

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/s10600-011-9785-8'

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/s10600-011-9785-8'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s10600-011-9785-8'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s10600-011-9785-8'


 

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

81 TRIPLES      21 PREDICATES      28 URIs      19 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s10600-011-9785-8 schema:about anzsrc-for:03
2 anzsrc-for:0305
3 schema:author N112efde2262b4ec8a9a0c9483d98252a
4 schema:citation https://doi.org/10.1055/s-2006-957604
5 schema:datePublished 2011-01
6 schema:datePublishedReg 2011-01-01
7 schema:description A method was developed for lithiation of deoxypeganine. The reaction of organolithium deoxypeganine derivatives with isobutyraldehyde and benzaldehyde to produce its derivatives was studied. A chiral synthesis of substituted deoxypeganines was performed. The synthesized diastereomers and enantiomers were separated successfully using HPLC and a chiral column.
8 schema:genre non_research_article
9 schema:inLanguage en
10 schema:isAccessibleForFree false
11 schema:isPartOf N5b23552b42c547cba2cc15b9dff39a55
12 Nb788d23631f64c57b4956f92edd890ad
13 sg:journal.1009660
14 schema:name Lithiation of deoxypeganine and chiral synthesis of deoxypeganine derivatives
15 schema:pagination 929-931
16 schema:productId N10e8eadb75ec409ca61bccb04187b99f
17 N156b7ceca6dd4a37a95d49c0349ba27c
18 Nfdbf87e5e24a4675baf85862a21f0fe5
19 schema:sameAs https://app.dimensions.ai/details/publication/pub.1048769943
20 https://doi.org/10.1007/s10600-011-9785-8
21 schema:sdDatePublished 2019-04-10T17:33
22 schema:sdLicense https://scigraph.springernature.com/explorer/license/
23 schema:sdPublisher N1b85aa71142140e3bd93aa3281093aff
24 schema:url http://link.springer.com/10.1007%2Fs10600-011-9785-8
25 sgo:license sg:explorer/license/
26 sgo:sdDataset articles
27 rdf:type schema:ScholarlyArticle
28 N10e8eadb75ec409ca61bccb04187b99f schema:name dimensions_id
29 schema:value pub.1048769943
30 rdf:type schema:PropertyValue
31 N112efde2262b4ec8a9a0c9483d98252a rdf:first sg:person.015706066705.62
32 rdf:rest N91ca331e101b47a89a3d6bda9700ec20
33 N156b7ceca6dd4a37a95d49c0349ba27c schema:name readcube_id
34 schema:value e854a408ba295239346696145a9617270d8372f8b9324bbe6eef78a3394eff9e
35 rdf:type schema:PropertyValue
36 N1b85aa71142140e3bd93aa3281093aff schema:name Springer Nature - SN SciGraph project
37 rdf:type schema:Organization
38 N5b23552b42c547cba2cc15b9dff39a55 schema:issueNumber 6
39 rdf:type schema:PublicationIssue
40 N91ca331e101b47a89a3d6bda9700ec20 rdf:first sg:person.01125653241.38
41 rdf:rest Neb40b956bd384e40a431b4ae977e60d2
42 Nb788d23631f64c57b4956f92edd890ad schema:volumeNumber 46
43 rdf:type schema:PublicationVolume
44 Neb40b956bd384e40a431b4ae977e60d2 rdf:first sg:person.010304611115.11
45 rdf:rest rdf:nil
46 Nfdbf87e5e24a4675baf85862a21f0fe5 schema:name doi
47 schema:value 10.1007/s10600-011-9785-8
48 rdf:type schema:PropertyValue
49 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
50 schema:name Chemical Sciences
51 rdf:type schema:DefinedTerm
52 anzsrc-for:0305 schema:inDefinedTermSet anzsrc-for:
53 schema:name Organic Chemistry
54 rdf:type schema:DefinedTerm
55 sg:journal.1009660 schema:issn 0009-3130
56 1573-8388
57 schema:name Chemistry of Natural Compounds
58 rdf:type schema:Periodical
59 sg:person.010304611115.11 schema:affiliation https://www.grid.ac/institutes/grid.419209.7
60 schema:familyName Ibragimov
61 schema:givenName T. F.
62 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010304611115.11
63 rdf:type schema:Person
64 sg:person.01125653241.38 schema:affiliation https://www.grid.ac/institutes/grid.11835.3e
65 schema:familyName Coldham
66 schema:givenName I.
67 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01125653241.38
68 rdf:type schema:Person
69 sg:person.015706066705.62 schema:affiliation https://www.grid.ac/institutes/grid.419209.7
70 schema:familyName Shakhidoyatov
71 schema:givenName Kh. M.
72 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015706066705.62
73 rdf:type schema:Person
74 https://doi.org/10.1055/s-2006-957604 schema:sameAs https://app.dimensions.ai/details/publication/pub.1057470628
75 rdf:type schema:CreativeWork
76 https://www.grid.ac/institutes/grid.11835.3e schema:alternateName University of Sheffield
77 schema:name Department of Chemistry, University of Sheffield, Brook Hill, S3 7HF, Sheffield, UK
78 rdf:type schema:Organization
79 https://www.grid.ac/institutes/grid.419209.7 schema:alternateName Academy of Sciences Republic of Uzbekistan
80 schema:name S. Yu. Yunusov Institute of the Chemistry of Plant Substances, Academy of Sciences of the Republic of Uzbekistan, Tashkent, Uzbekistan
81 rdf:type schema:Organization
 




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


...