Derivatives of 1-H-2-benzazepin-1-one as unusual products of the Hantsch reaction View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1998-10

AUTHORS

M. Plotnietse, N. Makarova, Yu. Popelis, G. Tirzitis

ABSTRACT

The use of opianic acid as the aldehyde component in the Hantsch reaction gives derivatives of 1-H-2-benzazepin-1-one instead of the expected 1,4-dihydropyridine derivatives.

PAGES

1198-1200

References to SciGraph publications

Journal

TITLE

Chemistry of Heterocyclic Compounds

ISSUE

10

VOLUME

34

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf02319502

DOI

http://dx.doi.org/10.1007/bf02319502

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1030895938


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", 
    "author": [
      {
        "familyName": "Plotnietse", 
        "givenName": "M.", 
        "id": "sg:person.012155141657.93", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012155141657.93"
        ], 
        "type": "Person"
      }, 
      {
        "familyName": "Makarova", 
        "givenName": "N.", 
        "id": "sg:person.015046316243.79", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015046316243.79"
        ], 
        "type": "Person"
      }, 
      {
        "familyName": "Popelis", 
        "givenName": "Yu.", 
        "id": "sg:person.07633020237.69", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07633020237.69"
        ], 
        "type": "Person"
      }, 
      {
        "familyName": "Tirzitis", 
        "givenName": "G.", 
        "id": "sg:person.01360231013.54", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01360231013.54"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "https://app.dimensions.ai/details/publication/pub.1044833097", 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/978-3-662-10207-7", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1044833097", 
          "https://doi.org/10.1007/978-3-662-10207-7"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/978-3-662-10207-7", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1044833097", 
          "https://doi.org/10.1007/978-3-662-10207-7"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm9600205", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055957449"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm9600205", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055957449"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jo01356a022", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056015353"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1097/00005344-199118101-00002", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1060205091"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1097/00005344-199118101-00002", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1060205091"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1097/00005344-199118101-00002", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1060205091"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.3987/rev-87-370", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1071779509"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "1998-10", 
    "datePublishedReg": "1998-10-01", 
    "description": "The use of opianic acid as the aldehyde component in the Hantsch reaction gives derivatives of 1-H-2-benzazepin-1-one instead of the expected 1,4-dihydropyridine derivatives.", 
    "genre": "non_research_article", 
    "id": "sg:pub.10.1007/bf02319502", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1356886", 
        "issn": [
          "0009-3122", 
          "1573-8353"
        ], 
        "name": "Chemistry of Heterocyclic Compounds", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "10", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "34"
      }
    ], 
    "name": "Derivatives of 1-H-2-benzazepin-1-one as unusual products of the Hantsch reaction", 
    "pagination": "1198-1200", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "932f2d1fb87977d01636428710b4fc789a9abae2742e0e1294ba9f9aa1e4ef32"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/bf02319502"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1030895938"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/bf02319502", 
      "https://app.dimensions.ai/details/publication/pub.1030895938"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-11T12:52", 
    "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/v90/0000000364_0000000364/records_72836_00000000.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "http://link.springer.com/10.1007%2FBF02319502"
  }
]
 

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/bf02319502'

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/bf02319502'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf02319502'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf02319502'


 

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

85 TRIPLES      20 PREDICATES      31 URIs      19 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/bf02319502 schema:author N29200db7f6f948748389400d65a4addb
2 schema:citation sg:pub.10.1007/978-3-662-10207-7
3 https://app.dimensions.ai/details/publication/pub.1044833097
4 https://doi.org/10.1021/jm9600205
5 https://doi.org/10.1021/jo01356a022
6 https://doi.org/10.1097/00005344-199118101-00002
7 https://doi.org/10.3987/rev-87-370
8 schema:datePublished 1998-10
9 schema:datePublishedReg 1998-10-01
10 schema:description The use of opianic acid as the aldehyde component in the Hantsch reaction gives derivatives of 1-H-2-benzazepin-1-one instead of the expected 1,4-dihydropyridine derivatives.
11 schema:genre non_research_article
12 schema:inLanguage en
13 schema:isAccessibleForFree false
14 schema:isPartOf N98e2534315924205b8e491cb914fd30c
15 Nd295e6f2cbd14805911cecb39eb6359a
16 sg:journal.1356886
17 schema:name Derivatives of 1-H-2-benzazepin-1-one as unusual products of the Hantsch reaction
18 schema:pagination 1198-1200
19 schema:productId Na4977f1af2d74b6f88c75afbb16555bf
20 Nac66aec873be48d4aa87b93a127676d2
21 Nc608d84bf8c643958d9c9e4ea20f4c3d
22 schema:sameAs https://app.dimensions.ai/details/publication/pub.1030895938
23 https://doi.org/10.1007/bf02319502
24 schema:sdDatePublished 2019-04-11T12:52
25 schema:sdLicense https://scigraph.springernature.com/explorer/license/
26 schema:sdPublisher N95f23b692cf344e196d1a95bf9210362
27 schema:url http://link.springer.com/10.1007%2FBF02319502
28 sgo:license sg:explorer/license/
29 sgo:sdDataset articles
30 rdf:type schema:ScholarlyArticle
31 N17f3203320e0418fa7f06c6c5f3c5085 rdf:first sg:person.07633020237.69
32 rdf:rest Ne683cca6e5734f54bdf03a6e22821486
33 N29200db7f6f948748389400d65a4addb rdf:first sg:person.012155141657.93
34 rdf:rest N3c010871a26c4522a434cdfa32c36f14
35 N3c010871a26c4522a434cdfa32c36f14 rdf:first sg:person.015046316243.79
36 rdf:rest N17f3203320e0418fa7f06c6c5f3c5085
37 N95f23b692cf344e196d1a95bf9210362 schema:name Springer Nature - SN SciGraph project
38 rdf:type schema:Organization
39 N98e2534315924205b8e491cb914fd30c schema:issueNumber 10
40 rdf:type schema:PublicationIssue
41 Na4977f1af2d74b6f88c75afbb16555bf schema:name doi
42 schema:value 10.1007/bf02319502
43 rdf:type schema:PropertyValue
44 Nac66aec873be48d4aa87b93a127676d2 schema:name readcube_id
45 schema:value 932f2d1fb87977d01636428710b4fc789a9abae2742e0e1294ba9f9aa1e4ef32
46 rdf:type schema:PropertyValue
47 Nc608d84bf8c643958d9c9e4ea20f4c3d schema:name dimensions_id
48 schema:value pub.1030895938
49 rdf:type schema:PropertyValue
50 Nd295e6f2cbd14805911cecb39eb6359a schema:volumeNumber 34
51 rdf:type schema:PublicationVolume
52 Ne683cca6e5734f54bdf03a6e22821486 rdf:first sg:person.01360231013.54
53 rdf:rest rdf:nil
54 sg:journal.1356886 schema:issn 0009-3122
55 1573-8353
56 schema:name Chemistry of Heterocyclic Compounds
57 rdf:type schema:Periodical
58 sg:person.012155141657.93 schema:familyName Plotnietse
59 schema:givenName M.
60 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012155141657.93
61 rdf:type schema:Person
62 sg:person.01360231013.54 schema:familyName Tirzitis
63 schema:givenName G.
64 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01360231013.54
65 rdf:type schema:Person
66 sg:person.015046316243.79 schema:familyName Makarova
67 schema:givenName N.
68 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015046316243.79
69 rdf:type schema:Person
70 sg:person.07633020237.69 schema:familyName Popelis
71 schema:givenName Yu.
72 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07633020237.69
73 rdf:type schema:Person
74 sg:pub.10.1007/978-3-662-10207-7 schema:sameAs https://app.dimensions.ai/details/publication/pub.1044833097
75 https://doi.org/10.1007/978-3-662-10207-7
76 rdf:type schema:CreativeWork
77 https://app.dimensions.ai/details/publication/pub.1044833097 schema:CreativeWork
78 https://doi.org/10.1021/jm9600205 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055957449
79 rdf:type schema:CreativeWork
80 https://doi.org/10.1021/jo01356a022 schema:sameAs https://app.dimensions.ai/details/publication/pub.1056015353
81 rdf:type schema:CreativeWork
82 https://doi.org/10.1097/00005344-199118101-00002 schema:sameAs https://app.dimensions.ai/details/publication/pub.1060205091
83 rdf:type schema:CreativeWork
84 https://doi.org/10.3987/rev-87-370 schema:sameAs https://app.dimensions.ai/details/publication/pub.1071779509
85 rdf:type schema:CreativeWork
 




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


...