Dioximes of 1,3-Diketones in the Trofimov Reaction: New 3-Substituted Pyrroles View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2005-06

AUTHORS

A. B. Zaitsev, E. Yu. Schmidt, A. M. Mikhaleva, A. V. Afonin, I. A. Ushakov

ABSTRACT

Dioximes of 1,3-diketones enter into the Trofimov reaction forming pyrroles containing an acyl or an O-vinyloxime substituent in position 3 of the pyrrole. In the case of sterically hindered dioximes the main reaction products are isoxazoles.

PAGES

722-729

References to SciGraph publications

Journal

TITLE

Chemistry of Heterocyclic Compounds

ISSUE

6

VOLUME

41

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-005-0212-6

DOI

http://dx.doi.org/10.1007/s10593-005-0212-6

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1049468964


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": [
      {
        "affiliation": {
          "alternateName": "A.E. Favorsky Irkutsk Institute of Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.465341.1", 
          "name": [
            "A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch, Russian Academy of Sciences, 664033, Irkutsk, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Zaitsev", 
        "givenName": "A. B.", 
        "id": "sg:person.014277023445.49", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014277023445.49"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "A.E. Favorsky Irkutsk Institute of Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.465341.1", 
          "name": [
            "A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch, Russian Academy of Sciences, 664033, Irkutsk, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Schmidt", 
        "givenName": "E. Yu.", 
        "id": "sg:person.015326620431.72", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015326620431.72"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "A.E. Favorsky Irkutsk Institute of Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.465341.1", 
          "name": [
            "A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch, Russian Academy of Sciences, 664033, Irkutsk, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Mikhaleva", 
        "givenName": "A. M.", 
        "id": "sg:person.07401046753.30", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07401046753.30"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "A.E. Favorsky Irkutsk Institute of Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.465341.1", 
          "name": [
            "A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch, Russian Academy of Sciences, 664033, Irkutsk, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Afonin", 
        "givenName": "A. V.", 
        "id": "sg:person.010460334133.39", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010460334133.39"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "A.E. Favorsky Irkutsk Institute of Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.465341.1", 
          "name": [
            "A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch, Russian Academy of Sciences, 664033, Irkutsk, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Ushakov", 
        "givenName": "I. A.", 
        "id": "sg:person.012070450113.34", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012070450113.34"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "https://doi.org/10.1016/s0960-894x(01)80155-4", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1001960005"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/hlca.19690520716", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1002986050"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0379-6779(98)00169-6", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1009987442"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/978-1-4613-0673-3_11", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1013309602", 
          "https://doi.org/10.1007/978-1-4613-0673-3_11"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/978-1-4613-0673-3_11", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1013309602", 
          "https://doi.org/10.1007/978-1-4613-0673-3_11"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/0040-4039(95)00016-6", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1018414120"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1139/v85-149", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1030296904"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0040-4020(02)01304-2", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1033362148"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0040-4020(02)01304-2", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1033362148"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/0379-6779(89)90517-1", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1034271899"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/0379-6779(89)90517-1", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1034271899"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0065-2725(08)60003-3", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1036161275"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0040-4020(01)82919-7", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1036686016"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1039/a703421k", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1037456263"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/cber.189803101115", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1037821121"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1039/c39890000475", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1041373159"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0379-6779(00)00250-2", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1044944552"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jo00032a011", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055962142"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jo00167a014", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055970670"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jo00261a027", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055975980"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jo00922a001", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055991481"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1055/s-2000-6330", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1057402768"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2005-06", 
    "datePublishedReg": "2005-06-01", 
    "description": "Dioximes of 1,3-diketones enter into the Trofimov reaction forming pyrroles containing an acyl or an O-vinyloxime substituent in position 3 of the pyrrole. In the case of sterically hindered dioximes the main reaction products are isoxazoles.", 
    "genre": "research_article", 
    "id": "sg:pub.10.1007/s10593-005-0212-6", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1356886", 
        "issn": [
          "0009-3122", 
          "1573-8353"
        ], 
        "name": "Chemistry of Heterocyclic Compounds", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "6", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "41"
      }
    ], 
    "name": "Dioximes of 1,3-Diketones in the Trofimov Reaction: New 3-Substituted Pyrroles", 
    "pagination": "722-729", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "eba89a0ca990fc2b6e0ddd3ef95bd791242d270afa6f476dd233ec342ab1f70a"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s10593-005-0212-6"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1049468964"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s10593-005-0212-6", 
      "https://app.dimensions.ai/details/publication/pub.1049468964"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-11T13:05", 
    "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/v90/0000000366_0000000366/records_112060_00000000.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "http://link.springer.com/10.1007%2Fs10593-005-0212-6"
  }
]
 

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/s10593-005-0212-6'

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/s10593-005-0212-6'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s10593-005-0212-6'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s10593-005-0212-6'


 

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

139 TRIPLES      20 PREDICATES      44 URIs      19 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s10593-005-0212-6 schema:author N0298fac784784fb6894c728e290c6c34
2 schema:citation sg:pub.10.1007/978-1-4613-0673-3_11
3 https://doi.org/10.1002/cber.189803101115
4 https://doi.org/10.1002/hlca.19690520716
5 https://doi.org/10.1016/0040-4039(95)00016-6
6 https://doi.org/10.1016/0379-6779(89)90517-1
7 https://doi.org/10.1016/s0040-4020(01)82919-7
8 https://doi.org/10.1016/s0040-4020(02)01304-2
9 https://doi.org/10.1016/s0065-2725(08)60003-3
10 https://doi.org/10.1016/s0379-6779(00)00250-2
11 https://doi.org/10.1016/s0379-6779(98)00169-6
12 https://doi.org/10.1016/s0960-894x(01)80155-4
13 https://doi.org/10.1021/jo00032a011
14 https://doi.org/10.1021/jo00167a014
15 https://doi.org/10.1021/jo00261a027
16 https://doi.org/10.1021/jo00922a001
17 https://doi.org/10.1039/a703421k
18 https://doi.org/10.1039/c39890000475
19 https://doi.org/10.1055/s-2000-6330
20 https://doi.org/10.1139/v85-149
21 schema:datePublished 2005-06
22 schema:datePublishedReg 2005-06-01
23 schema:description Dioximes of 1,3-diketones enter into the Trofimov reaction forming pyrroles containing an acyl or an O-vinyloxime substituent in position 3 of the pyrrole. In the case of sterically hindered dioximes the main reaction products are isoxazoles.
24 schema:genre research_article
25 schema:inLanguage en
26 schema:isAccessibleForFree false
27 schema:isPartOf N7b32ca87ca3e4d09a679e6a5d750ccf9
28 Nd06c8537a41b4b49b4bc55e8ed83734a
29 sg:journal.1356886
30 schema:name Dioximes of 1,3-Diketones in the Trofimov Reaction: New 3-Substituted Pyrroles
31 schema:pagination 722-729
32 schema:productId N0698e5d6a55c4e6fbb8ff89103c2f596
33 Na3659a3c66094efa8bd177c07f5a771f
34 Nd1b39c1685144c758a60514c7de25bff
35 schema:sameAs https://app.dimensions.ai/details/publication/pub.1049468964
36 https://doi.org/10.1007/s10593-005-0212-6
37 schema:sdDatePublished 2019-04-11T13:05
38 schema:sdLicense https://scigraph.springernature.com/explorer/license/
39 schema:sdPublisher Nf9d4219f4e0345488cc31d37af599142
40 schema:url http://link.springer.com/10.1007%2Fs10593-005-0212-6
41 sgo:license sg:explorer/license/
42 sgo:sdDataset articles
43 rdf:type schema:ScholarlyArticle
44 N0298fac784784fb6894c728e290c6c34 rdf:first sg:person.014277023445.49
45 rdf:rest Nc73b84ee19d2454c959fd436f440b718
46 N0698e5d6a55c4e6fbb8ff89103c2f596 schema:name dimensions_id
47 schema:value pub.1049468964
48 rdf:type schema:PropertyValue
49 N246b24e0e06f4ed1b6c9eb909cb731df rdf:first sg:person.07401046753.30
50 rdf:rest Nff33f10e51aa4303989d02ac1afb1080
51 N7b32ca87ca3e4d09a679e6a5d750ccf9 schema:issueNumber 6
52 rdf:type schema:PublicationIssue
53 Na3659a3c66094efa8bd177c07f5a771f schema:name readcube_id
54 schema:value eba89a0ca990fc2b6e0ddd3ef95bd791242d270afa6f476dd233ec342ab1f70a
55 rdf:type schema:PropertyValue
56 Nc73b84ee19d2454c959fd436f440b718 rdf:first sg:person.015326620431.72
57 rdf:rest N246b24e0e06f4ed1b6c9eb909cb731df
58 Nd06c8537a41b4b49b4bc55e8ed83734a schema:volumeNumber 41
59 rdf:type schema:PublicationVolume
60 Nd1b39c1685144c758a60514c7de25bff schema:name doi
61 schema:value 10.1007/s10593-005-0212-6
62 rdf:type schema:PropertyValue
63 Nf9d4219f4e0345488cc31d37af599142 schema:name Springer Nature - SN SciGraph project
64 rdf:type schema:Organization
65 Nfe4b1a905b1741eca648780f3b5b9c6c rdf:first sg:person.012070450113.34
66 rdf:rest rdf:nil
67 Nff33f10e51aa4303989d02ac1afb1080 rdf:first sg:person.010460334133.39
68 rdf:rest Nfe4b1a905b1741eca648780f3b5b9c6c
69 sg:journal.1356886 schema:issn 0009-3122
70 1573-8353
71 schema:name Chemistry of Heterocyclic Compounds
72 rdf:type schema:Periodical
73 sg:person.010460334133.39 schema:affiliation https://www.grid.ac/institutes/grid.465341.1
74 schema:familyName Afonin
75 schema:givenName A. V.
76 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010460334133.39
77 rdf:type schema:Person
78 sg:person.012070450113.34 schema:affiliation https://www.grid.ac/institutes/grid.465341.1
79 schema:familyName Ushakov
80 schema:givenName I. A.
81 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012070450113.34
82 rdf:type schema:Person
83 sg:person.014277023445.49 schema:affiliation https://www.grid.ac/institutes/grid.465341.1
84 schema:familyName Zaitsev
85 schema:givenName A. B.
86 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014277023445.49
87 rdf:type schema:Person
88 sg:person.015326620431.72 schema:affiliation https://www.grid.ac/institutes/grid.465341.1
89 schema:familyName Schmidt
90 schema:givenName E. Yu.
91 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015326620431.72
92 rdf:type schema:Person
93 sg:person.07401046753.30 schema:affiliation https://www.grid.ac/institutes/grid.465341.1
94 schema:familyName Mikhaleva
95 schema:givenName A. M.
96 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07401046753.30
97 rdf:type schema:Person
98 sg:pub.10.1007/978-1-4613-0673-3_11 schema:sameAs https://app.dimensions.ai/details/publication/pub.1013309602
99 https://doi.org/10.1007/978-1-4613-0673-3_11
100 rdf:type schema:CreativeWork
101 https://doi.org/10.1002/cber.189803101115 schema:sameAs https://app.dimensions.ai/details/publication/pub.1037821121
102 rdf:type schema:CreativeWork
103 https://doi.org/10.1002/hlca.19690520716 schema:sameAs https://app.dimensions.ai/details/publication/pub.1002986050
104 rdf:type schema:CreativeWork
105 https://doi.org/10.1016/0040-4039(95)00016-6 schema:sameAs https://app.dimensions.ai/details/publication/pub.1018414120
106 rdf:type schema:CreativeWork
107 https://doi.org/10.1016/0379-6779(89)90517-1 schema:sameAs https://app.dimensions.ai/details/publication/pub.1034271899
108 rdf:type schema:CreativeWork
109 https://doi.org/10.1016/s0040-4020(01)82919-7 schema:sameAs https://app.dimensions.ai/details/publication/pub.1036686016
110 rdf:type schema:CreativeWork
111 https://doi.org/10.1016/s0040-4020(02)01304-2 schema:sameAs https://app.dimensions.ai/details/publication/pub.1033362148
112 rdf:type schema:CreativeWork
113 https://doi.org/10.1016/s0065-2725(08)60003-3 schema:sameAs https://app.dimensions.ai/details/publication/pub.1036161275
114 rdf:type schema:CreativeWork
115 https://doi.org/10.1016/s0379-6779(00)00250-2 schema:sameAs https://app.dimensions.ai/details/publication/pub.1044944552
116 rdf:type schema:CreativeWork
117 https://doi.org/10.1016/s0379-6779(98)00169-6 schema:sameAs https://app.dimensions.ai/details/publication/pub.1009987442
118 rdf:type schema:CreativeWork
119 https://doi.org/10.1016/s0960-894x(01)80155-4 schema:sameAs https://app.dimensions.ai/details/publication/pub.1001960005
120 rdf:type schema:CreativeWork
121 https://doi.org/10.1021/jo00032a011 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055962142
122 rdf:type schema:CreativeWork
123 https://doi.org/10.1021/jo00167a014 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055970670
124 rdf:type schema:CreativeWork
125 https://doi.org/10.1021/jo00261a027 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055975980
126 rdf:type schema:CreativeWork
127 https://doi.org/10.1021/jo00922a001 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055991481
128 rdf:type schema:CreativeWork
129 https://doi.org/10.1039/a703421k schema:sameAs https://app.dimensions.ai/details/publication/pub.1037456263
130 rdf:type schema:CreativeWork
131 https://doi.org/10.1039/c39890000475 schema:sameAs https://app.dimensions.ai/details/publication/pub.1041373159
132 rdf:type schema:CreativeWork
133 https://doi.org/10.1055/s-2000-6330 schema:sameAs https://app.dimensions.ai/details/publication/pub.1057402768
134 rdf:type schema:CreativeWork
135 https://doi.org/10.1139/v85-149 schema:sameAs https://app.dimensions.ai/details/publication/pub.1030296904
136 rdf:type schema:CreativeWork
137 https://www.grid.ac/institutes/grid.465341.1 schema:alternateName A.E. Favorsky Irkutsk Institute of Chemistry
138 schema:name A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch, Russian Academy of Sciences, 664033, Irkutsk, Russia
139 rdf:type schema:Organization
 




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


...