Specificity of the Reaction of Tetranitromethane with Alkenes in Nitromethane View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2005-09

AUTHORS

O. A. Ivanova, E. B. Averina, E. M. Budynina, A. A. Korlyukov, M. Yu. Antipin, T. S. Kuznetsova, N. S. Zefirov

ABSTRACT

Reactions of tetranitromethane with a number of di- and trisubstituted olefins in nitromethane were studied. Vinylcyclopropanes and phenylcycloalkenes reacted with tetranitromethane in an unexpected fashion, leading to formation of alkyltrinitromethanes and vicinal nitro alcohols.

PAGES

1265-1270

Journal

TITLE

Russian Journal of Organic Chemistry

ISSUE

9

VOLUME

41

Author Affiliations

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11178-005-0333-5

DOI

http://dx.doi.org/10.1007/s11178-005-0333-5

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1036021836


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": "Moscow State University", 
          "id": "https://www.grid.ac/institutes/grid.14476.30", 
          "name": [
            "Faculty of Chemistry, Moscow State University, Vorob'evy gory 1, 119899, Moscow, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Ivanova", 
        "givenName": "O. A.", 
        "id": "sg:person.01171566717.93", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01171566717.93"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Moscow State University", 
          "id": "https://www.grid.ac/institutes/grid.14476.30", 
          "name": [
            "Faculty of Chemistry, Moscow State University, Vorob'evy gory 1, 119899, Moscow, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Averina", 
        "givenName": "E. B.", 
        "id": "sg:person.01245745462.24", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01245745462.24"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Moscow State University", 
          "id": "https://www.grid.ac/institutes/grid.14476.30", 
          "name": [
            "Faculty of Chemistry, Moscow State University, Vorob'evy gory 1, 119899, Moscow, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Budynina", 
        "givenName": "E. M.", 
        "id": "sg:person.014123435161.41", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014123435161.41"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Moscow State University", 
          "id": "https://www.grid.ac/institutes/grid.14476.30", 
          "name": [
            "Faculty of Chemistry, Moscow State University, Vorob'evy gory 1, 119899, Moscow, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Korlyukov", 
        "givenName": "A. A.", 
        "id": "sg:person.015723577636.56", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015723577636.56"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Moscow State University", 
          "id": "https://www.grid.ac/institutes/grid.14476.30", 
          "name": [
            "Faculty of Chemistry, Moscow State University, Vorob'evy gory 1, 119899, Moscow, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Antipin", 
        "givenName": "M. Yu.", 
        "id": "sg:person.010142146727.55", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010142146727.55"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Moscow State University", 
          "id": "https://www.grid.ac/institutes/grid.14476.30", 
          "name": [
            "Faculty of Chemistry, Moscow State University, Vorob'evy gory 1, 119899, Moscow, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Kuznetsova", 
        "givenName": "T. S.", 
        "id": "sg:person.010375672121.37", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010375672121.37"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Moscow State University", 
          "id": "https://www.grid.ac/institutes/grid.14476.30", 
          "name": [
            "Faculty of Chemistry, Moscow State University, Vorob'evy gory 1, 119899, Moscow, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Zefirov", 
        "givenName": "N. S.", 
        "id": "sg:person.010726101355.80", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010726101355.80"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "sg:pub.10.1023/b:rujo.0000034936.03355.d1", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1006742285", 
          "https://doi.org/10.1023/b:rujo.0000034936.03355.d1"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1039/jr9560004280", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1009090415"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1139/v67-113", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1045334195"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ja01003a013", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055760387"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jo00064a025", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055964238"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2005-09", 
    "datePublishedReg": "2005-09-01", 
    "description": "Reactions of tetranitromethane with a number of di- and trisubstituted olefins in nitromethane were studied. Vinylcyclopropanes and phenylcycloalkenes reacted with tetranitromethane in an unexpected fashion, leading to formation of alkyltrinitromethanes and vicinal nitro alcohols.", 
    "genre": "research_article", 
    "id": "sg:pub.10.1007/s11178-005-0333-5", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1136317", 
        "issn": [
          "1070-4280", 
          "1608-3393"
        ], 
        "name": "Russian Journal of Organic Chemistry", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "9", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "41"
      }
    ], 
    "name": "Specificity of the Reaction of Tetranitromethane with Alkenes in Nitromethane", 
    "pagination": "1265-1270", 
    "productId": [
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s11178-005-0333-5"
        ]
      }, 
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "ab9829a74da7d8d06192d43c36f9cd614e2130d528647dc5b30664507eb4ff15"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1036021836"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s11178-005-0333-5", 
      "https://app.dimensions.ai/details/publication/pub.1036021836"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-15T08:53", 
    "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/v90/0000000374_0000000374/records_119750_00000000.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "http://link.springer.com/10.1007%2Fs11178-005-0333-5"
  }
]
 

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/s11178-005-0333-5'

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/s11178-005-0333-5'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s11178-005-0333-5'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s11178-005-0333-5'


 

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

111 TRIPLES      20 PREDICATES      30 URIs      19 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s11178-005-0333-5 schema:author Nc292b9f152214f63a471bbed820bb974
2 schema:citation sg:pub.10.1023/b:rujo.0000034936.03355.d1
3 https://doi.org/10.1021/ja01003a013
4 https://doi.org/10.1021/jo00064a025
5 https://doi.org/10.1039/jr9560004280
6 https://doi.org/10.1139/v67-113
7 schema:datePublished 2005-09
8 schema:datePublishedReg 2005-09-01
9 schema:description Reactions of tetranitromethane with a number of di- and trisubstituted olefins in nitromethane were studied. Vinylcyclopropanes and phenylcycloalkenes reacted with tetranitromethane in an unexpected fashion, leading to formation of alkyltrinitromethanes and vicinal nitro alcohols.
10 schema:genre research_article
11 schema:inLanguage en
12 schema:isAccessibleForFree false
13 schema:isPartOf N59c2103a3fba4591a570c1f9db2ef6fd
14 N9d19c5c25ed246e69bd61043ef3009d0
15 sg:journal.1136317
16 schema:name Specificity of the Reaction of Tetranitromethane with Alkenes in Nitromethane
17 schema:pagination 1265-1270
18 schema:productId N33139e2262b14aaa9987755f090414b2
19 N67dbade4e2a949caa8c6692359264e5c
20 Ne3b1cf4829034e1ba787283cadebe0b0
21 schema:sameAs https://app.dimensions.ai/details/publication/pub.1036021836
22 https://doi.org/10.1007/s11178-005-0333-5
23 schema:sdDatePublished 2019-04-15T08:53
24 schema:sdLicense https://scigraph.springernature.com/explorer/license/
25 schema:sdPublisher Nd969d3fe0f0844f490c73928e94632d8
26 schema:url http://link.springer.com/10.1007%2Fs11178-005-0333-5
27 sgo:license sg:explorer/license/
28 sgo:sdDataset articles
29 rdf:type schema:ScholarlyArticle
30 N030582b3d92049d98c79e316b7b9ade1 rdf:first sg:person.010375672121.37
31 rdf:rest Nc7873acfe16043b399581ff45fb4df67
32 N33139e2262b14aaa9987755f090414b2 schema:name doi
33 schema:value 10.1007/s11178-005-0333-5
34 rdf:type schema:PropertyValue
35 N5795a6bc3a5c4412b606b825ea174ba1 rdf:first sg:person.010142146727.55
36 rdf:rest N030582b3d92049d98c79e316b7b9ade1
37 N59c2103a3fba4591a570c1f9db2ef6fd schema:volumeNumber 41
38 rdf:type schema:PublicationVolume
39 N67dbade4e2a949caa8c6692359264e5c schema:name readcube_id
40 schema:value ab9829a74da7d8d06192d43c36f9cd614e2130d528647dc5b30664507eb4ff15
41 rdf:type schema:PropertyValue
42 N8fa1d34528034a088cc9f70d84f90c4f rdf:first sg:person.015723577636.56
43 rdf:rest N5795a6bc3a5c4412b606b825ea174ba1
44 N9d19c5c25ed246e69bd61043ef3009d0 schema:issueNumber 9
45 rdf:type schema:PublicationIssue
46 N9e0ca339fe164bb7a747680a7008563d rdf:first sg:person.01245745462.24
47 rdf:rest Nf3e740dbb15f44a184d16c3813819518
48 Nc292b9f152214f63a471bbed820bb974 rdf:first sg:person.01171566717.93
49 rdf:rest N9e0ca339fe164bb7a747680a7008563d
50 Nc7873acfe16043b399581ff45fb4df67 rdf:first sg:person.010726101355.80
51 rdf:rest rdf:nil
52 Nd969d3fe0f0844f490c73928e94632d8 schema:name Springer Nature - SN SciGraph project
53 rdf:type schema:Organization
54 Ne3b1cf4829034e1ba787283cadebe0b0 schema:name dimensions_id
55 schema:value pub.1036021836
56 rdf:type schema:PropertyValue
57 Nf3e740dbb15f44a184d16c3813819518 rdf:first sg:person.014123435161.41
58 rdf:rest N8fa1d34528034a088cc9f70d84f90c4f
59 sg:journal.1136317 schema:issn 1070-4280
60 1608-3393
61 schema:name Russian Journal of Organic Chemistry
62 rdf:type schema:Periodical
63 sg:person.010142146727.55 schema:affiliation https://www.grid.ac/institutes/grid.14476.30
64 schema:familyName Antipin
65 schema:givenName M. Yu.
66 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010142146727.55
67 rdf:type schema:Person
68 sg:person.010375672121.37 schema:affiliation https://www.grid.ac/institutes/grid.14476.30
69 schema:familyName Kuznetsova
70 schema:givenName T. S.
71 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010375672121.37
72 rdf:type schema:Person
73 sg:person.010726101355.80 schema:affiliation https://www.grid.ac/institutes/grid.14476.30
74 schema:familyName Zefirov
75 schema:givenName N. S.
76 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010726101355.80
77 rdf:type schema:Person
78 sg:person.01171566717.93 schema:affiliation https://www.grid.ac/institutes/grid.14476.30
79 schema:familyName Ivanova
80 schema:givenName O. A.
81 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01171566717.93
82 rdf:type schema:Person
83 sg:person.01245745462.24 schema:affiliation https://www.grid.ac/institutes/grid.14476.30
84 schema:familyName Averina
85 schema:givenName E. B.
86 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01245745462.24
87 rdf:type schema:Person
88 sg:person.014123435161.41 schema:affiliation https://www.grid.ac/institutes/grid.14476.30
89 schema:familyName Budynina
90 schema:givenName E. M.
91 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014123435161.41
92 rdf:type schema:Person
93 sg:person.015723577636.56 schema:affiliation https://www.grid.ac/institutes/grid.14476.30
94 schema:familyName Korlyukov
95 schema:givenName A. A.
96 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015723577636.56
97 rdf:type schema:Person
98 sg:pub.10.1023/b:rujo.0000034936.03355.d1 schema:sameAs https://app.dimensions.ai/details/publication/pub.1006742285
99 https://doi.org/10.1023/b:rujo.0000034936.03355.d1
100 rdf:type schema:CreativeWork
101 https://doi.org/10.1021/ja01003a013 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055760387
102 rdf:type schema:CreativeWork
103 https://doi.org/10.1021/jo00064a025 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055964238
104 rdf:type schema:CreativeWork
105 https://doi.org/10.1039/jr9560004280 schema:sameAs https://app.dimensions.ai/details/publication/pub.1009090415
106 rdf:type schema:CreativeWork
107 https://doi.org/10.1139/v67-113 schema:sameAs https://app.dimensions.ai/details/publication/pub.1045334195
108 rdf:type schema:CreativeWork
109 https://www.grid.ac/institutes/grid.14476.30 schema:alternateName Moscow State University
110 schema:name Faculty of Chemistry, Moscow State University, Vorob'evy gory 1, 119899, Moscow, Russia
111 rdf:type schema:Organization
 




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


...