Pictet–Spengler reaction in the synthesis of condensed benzodiazepines: synthesis of 11-hetaryl derivatives of 11,12-dihydroquinazolino[3,2-c][2,3]benzodiazepin-14(6H)-ones View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2017-04

AUTHORS

Andrey S. Tolkunov, Alexander V. Mazepa, Gennadiy V. Palamarchuk, Oleg V. Shishkin, Sergey Yu. Sujkov, Sergey L. Bogza

ABSTRACT

New derivatives of 11,12-dihydroquinazolino[3,2-c][2,3]benzodiazepin-14(6H)-one have been synthesized. 11-(2-Thienyl)- and 11-(5-R-2-furyl)-substituted compounds were prepared by the Pictet–Spengler reaction of 3-amino-2-(3,4-dimethoxybenzyl)quinazolin-4(3H)-one with heterocyclic aldehydes in aprotic media. Their chemical structures were confirmed by 1H and 13C NMR spectroscopy and mass spectrometry. We observed the opening of diazepine ring in 8,9-dimethoxy-11-(5-chloro-2-furyl)-11,12-dihydroquinazolino[3,2-c][2,3]benzodiazepin-14(6H)-one when treated with trifluoroacetic acid, and the structure of the product was determined by NMR (1H, 13C, HSQC, HMBC experiments) and mass spectrometry data. The crystal structure of 3-amino-2-[4,5-dimethoxy-2-[(5-oxofuran-2(5H)-yliden)methyl]benzyl]quinazolin-4(3H)-one was confirmed by single-crystal X-ray analysis. More... »

PAGES

695-701

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00706-016-1861-0

DOI

http://dx.doi.org/10.1007/s00706-016-1861-0

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1083877093


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/2008/0306", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Physical Chemistry (incl. Structural)", 
        "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": {
          "name": [
            "L. M. Litvinenko Institute of Physical-Organic Chemistry and Coal Chemistry, 50 Kharkivske shose, 02160, Kiev, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Tolkunov", 
        "givenName": "Andrey S.", 
        "id": "sg:person.014040034526.14", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014040034526.14"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Physical-Chemical Institute O. Bogatsky", 
          "id": "https://www.grid.ac/institutes/grid.493162.b", 
          "name": [
            "A.V. Bogatsky Physico-Chemical Institute, 86 Lustdorfska Str., 65080, Odessa, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Mazepa", 
        "givenName": "Alexander V.", 
        "id": "sg:person.010722472163.16", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010722472163.16"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "University of Kharkiv", 
          "id": "https://www.grid.ac/institutes/grid.18999.30", 
          "name": [
            "V. N. Karazin Kharkiv National University, 4 Svobody Sq., 61022, Kharkiv, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Palamarchuk", 
        "givenName": "Gennadiy V.", 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "University of Kharkiv", 
          "id": "https://www.grid.ac/institutes/grid.18999.30", 
          "name": [
            "V. N. Karazin Kharkiv National University, 4 Svobody Sq., 61022, Kharkiv, Ukraine", 
            "SSI \u201cInstitute for Single Crystals\u201d, 60 Nauky ave., 61001, Kharkiv, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Shishkin", 
        "givenName": "Oleg V.", 
        "id": "sg:person.01023575604.49", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01023575604.49"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Organic Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.464621.3", 
          "name": [
            "Institute of Organic Chemistry, 5 Murmanska Str., 02660, Kiev, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Sujkov", 
        "givenName": "Sergey Yu.", 
        "id": "sg:person.07525304726.05", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07525304726.05"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Institute of Organic Chemistry", 
          "id": "https://www.grid.ac/institutes/grid.464621.3", 
          "name": [
            "Institute of Organic Chemistry, 5 Murmanska Str., 02660, Kiev, Ukraine"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Bogza", 
        "givenName": "Sergey L.", 
        "id": "sg:person.010322665326.29", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010322665326.29"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "sg:pub.10.1007/s10593-010-0550-x", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1014921473", 
          "https://doi.org/10.1007/s10593-010-0550-x"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s10593-010-0550-x", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1014921473", 
          "https://doi.org/10.1007/s10593-010-0550-x"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm001012y", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1016415703"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm001012y", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1016415703"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0301-0082(99)00020-9", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1019401498"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0968-0896(00)00133-4", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1021152352"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0014-827x(99)00022-1", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1022172717"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/cmdc.200600144", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1023004603"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s10593-010-0573-3", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1025978009", 
          "https://doi.org/10.1007/s10593-010-0573-3"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s10593-010-0573-3", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1025978009", 
          "https://doi.org/10.1007/s10593-010-0573-3"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1107/s0108767307043930", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1027786902"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0014-827x(01)01186-7", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1030205664"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/cber.19741071219", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1030617658"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0040-4039(01)01602-1", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1034467725"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/0896-6273(93)90241-i", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1039384809"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1039/p19840000849", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1040384628"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0960-894x(98)00148-6", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1043107171"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0960-894x(00)00693-4", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1043718235"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.bmcl.2005.09.029", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1047267310"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.bmcl.2005.09.029", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1047267310"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm030821p", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055948283"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm030821p", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055948283"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm050552y", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055949680"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm050552y", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055949680"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm0580003", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055950073"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm0580003", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055950073"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm960506l", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055957815"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm960506l", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055957815"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm980168j", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055958807"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm980168j", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055958807"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1358/dof.2001.026.08.630957", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1065061504"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.3987/com-99-8487", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1071774297"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://app.dimensions.ai/details/publication/pub.1077007229", 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2017-04", 
    "datePublishedReg": "2017-04-01", 
    "description": "New derivatives of 11,12-dihydroquinazolino[3,2-c][2,3]benzodiazepin-14(6H)-one have been synthesized. 11-(2-Thienyl)- and 11-(5-R-2-furyl)-substituted compounds were prepared by the Pictet\u2013Spengler reaction of 3-amino-2-(3,4-dimethoxybenzyl)quinazolin-4(3H)-one with heterocyclic aldehydes in aprotic media. Their chemical structures were confirmed by 1H and 13C NMR spectroscopy and mass spectrometry. We observed the opening of diazepine ring in 8,9-dimethoxy-11-(5-chloro-2-furyl)-11,12-dihydroquinazolino[3,2-c][2,3]benzodiazepin-14(6H)-one when treated with trifluoroacetic acid, and the structure of the product was determined by NMR (1H, 13C, HSQC, HMBC experiments) and mass spectrometry data. The crystal structure of 3-amino-2-[4,5-dimethoxy-2-[(5-oxofuran-2(5H)-yliden)methyl]benzyl]quinazolin-4(3H)-one was confirmed by single-crystal X-ray analysis. ", 
    "genre": "research_article", 
    "id": "sg:pub.10.1007/s00706-016-1861-0", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1345587", 
        "issn": [
          "0343-7329", 
          "0026-9247"
        ], 
        "name": "Monatshefte f\u00fcr Chemie - Chemical Monthly", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "4", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "148"
      }
    ], 
    "name": "Pictet\u2013Spengler reaction in the synthesis of condensed benzodiazepines: synthesis of 11-hetaryl derivatives of 11,12-dihydroquinazolino[3,2-c][2,3]benzodiazepin-14(6H)-ones", 
    "pagination": "695-701", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "3c6e6ad4bf9d39cc7ef86ff553cb23abb76b2c9c77b0b827b1f0b8f5942ea7a8"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s00706-016-1861-0"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1083877093"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s00706-016-1861-0", 
      "https://app.dimensions.ai/details/publication/pub.1083877093"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-11T10:01", 
    "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/v90/0000000347_0000000347/records_89819_00000002.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://link.springer.com/10.1007%2Fs00706-016-1861-0"
  }
]
 

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/s00706-016-1861-0'

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/s00706-016-1861-0'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s00706-016-1861-0'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s00706-016-1861-0'


 

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

177 TRIPLES      21 PREDICATES      51 URIs      19 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s00706-016-1861-0 schema:about anzsrc-for:03
2 anzsrc-for:0306
3 schema:author N61471059cf7f4bcbb6be3f4f1ce1924f
4 schema:citation sg:pub.10.1007/s10593-010-0550-x
5 sg:pub.10.1007/s10593-010-0573-3
6 https://app.dimensions.ai/details/publication/pub.1077007229
7 https://doi.org/10.1002/cber.19741071219
8 https://doi.org/10.1002/cmdc.200600144
9 https://doi.org/10.1016/0896-6273(93)90241-i
10 https://doi.org/10.1016/j.bmcl.2005.09.029
11 https://doi.org/10.1016/s0014-827x(01)01186-7
12 https://doi.org/10.1016/s0014-827x(99)00022-1
13 https://doi.org/10.1016/s0040-4039(01)01602-1
14 https://doi.org/10.1016/s0301-0082(99)00020-9
15 https://doi.org/10.1016/s0960-894x(00)00693-4
16 https://doi.org/10.1016/s0960-894x(98)00148-6
17 https://doi.org/10.1016/s0968-0896(00)00133-4
18 https://doi.org/10.1021/jm001012y
19 https://doi.org/10.1021/jm030821p
20 https://doi.org/10.1021/jm050552y
21 https://doi.org/10.1021/jm0580003
22 https://doi.org/10.1021/jm960506l
23 https://doi.org/10.1021/jm980168j
24 https://doi.org/10.1039/p19840000849
25 https://doi.org/10.1107/s0108767307043930
26 https://doi.org/10.1358/dof.2001.026.08.630957
27 https://doi.org/10.3987/com-99-8487
28 schema:datePublished 2017-04
29 schema:datePublishedReg 2017-04-01
30 schema:description New derivatives of 11,12-dihydroquinazolino[3,2-c][2,3]benzodiazepin-14(6H)-one have been synthesized. 11-(2-Thienyl)- and 11-(5-R-2-furyl)-substituted compounds were prepared by the Pictet–Spengler reaction of 3-amino-2-(3,4-dimethoxybenzyl)quinazolin-4(3H)-one with heterocyclic aldehydes in aprotic media. Their chemical structures were confirmed by 1H and 13C NMR spectroscopy and mass spectrometry. We observed the opening of diazepine ring in 8,9-dimethoxy-11-(5-chloro-2-furyl)-11,12-dihydroquinazolino[3,2-c][2,3]benzodiazepin-14(6H)-one when treated with trifluoroacetic acid, and the structure of the product was determined by NMR (1H, 13C, HSQC, HMBC experiments) and mass spectrometry data. The crystal structure of 3-amino-2-[4,5-dimethoxy-2-[(5-oxofuran-2(5H)-yliden)methyl]benzyl]quinazolin-4(3H)-one was confirmed by single-crystal X-ray analysis.
31 schema:genre research_article
32 schema:inLanguage en
33 schema:isAccessibleForFree false
34 schema:isPartOf N07149a62b6324996a875fc018958dc7b
35 N85039fe6f86444609e5e9aa12cb3307e
36 sg:journal.1345587
37 schema:name Pictet–Spengler reaction in the synthesis of condensed benzodiazepines: synthesis of 11-hetaryl derivatives of 11,12-dihydroquinazolino[3,2-c][2,3]benzodiazepin-14(6H)-ones
38 schema:pagination 695-701
39 schema:productId N436ed85738254effba171a910df518d3
40 N8f4bffd5b26e4a1c8ddbac4b87b0a32d
41 Na4768b282b194b78ba89a8d150b8fcbf
42 schema:sameAs https://app.dimensions.ai/details/publication/pub.1083877093
43 https://doi.org/10.1007/s00706-016-1861-0
44 schema:sdDatePublished 2019-04-11T10:01
45 schema:sdLicense https://scigraph.springernature.com/explorer/license/
46 schema:sdPublisher N938ec3235b524506a5af8258c0ba6310
47 schema:url https://link.springer.com/10.1007%2Fs00706-016-1861-0
48 sgo:license sg:explorer/license/
49 sgo:sdDataset articles
50 rdf:type schema:ScholarlyArticle
51 N01214670c9ff4270944dda4f94133319 schema:name L. M. Litvinenko Institute of Physical-Organic Chemistry and Coal Chemistry, 50 Kharkivske shose, 02160, Kiev, Ukraine
52 rdf:type schema:Organization
53 N07149a62b6324996a875fc018958dc7b schema:volumeNumber 148
54 rdf:type schema:PublicationVolume
55 N266dc76c11674ff6bd499f3a7d4d09ab rdf:first N9f9c946829a6464a9dd8cae1c92cdfaa
56 rdf:rest N7fee8c70f0e84c8fb0990048b8cc63dc
57 N436ed85738254effba171a910df518d3 schema:name doi
58 schema:value 10.1007/s00706-016-1861-0
59 rdf:type schema:PropertyValue
60 N61471059cf7f4bcbb6be3f4f1ce1924f rdf:first sg:person.014040034526.14
61 rdf:rest Nc80f4204c80a4eabbf245142a317124f
62 N7fee8c70f0e84c8fb0990048b8cc63dc rdf:first sg:person.01023575604.49
63 rdf:rest Nde8891668e444bf996d728c21094bc53
64 N85039fe6f86444609e5e9aa12cb3307e schema:issueNumber 4
65 rdf:type schema:PublicationIssue
66 N870b73dbc2054bc98e180ba880993278 rdf:first sg:person.010322665326.29
67 rdf:rest rdf:nil
68 N8f4bffd5b26e4a1c8ddbac4b87b0a32d schema:name dimensions_id
69 schema:value pub.1083877093
70 rdf:type schema:PropertyValue
71 N938ec3235b524506a5af8258c0ba6310 schema:name Springer Nature - SN SciGraph project
72 rdf:type schema:Organization
73 N9f9c946829a6464a9dd8cae1c92cdfaa schema:affiliation https://www.grid.ac/institutes/grid.18999.30
74 schema:familyName Palamarchuk
75 schema:givenName Gennadiy V.
76 rdf:type schema:Person
77 Na4768b282b194b78ba89a8d150b8fcbf schema:name readcube_id
78 schema:value 3c6e6ad4bf9d39cc7ef86ff553cb23abb76b2c9c77b0b827b1f0b8f5942ea7a8
79 rdf:type schema:PropertyValue
80 Nc80f4204c80a4eabbf245142a317124f rdf:first sg:person.010722472163.16
81 rdf:rest N266dc76c11674ff6bd499f3a7d4d09ab
82 Nde8891668e444bf996d728c21094bc53 rdf:first sg:person.07525304726.05
83 rdf:rest N870b73dbc2054bc98e180ba880993278
84 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
85 schema:name Chemical Sciences
86 rdf:type schema:DefinedTerm
87 anzsrc-for:0306 schema:inDefinedTermSet anzsrc-for:
88 schema:name Physical Chemistry (incl. Structural)
89 rdf:type schema:DefinedTerm
90 sg:journal.1345587 schema:issn 0026-9247
91 0343-7329
92 schema:name Monatshefte für Chemie - Chemical Monthly
93 rdf:type schema:Periodical
94 sg:person.01023575604.49 schema:affiliation https://www.grid.ac/institutes/grid.18999.30
95 schema:familyName Shishkin
96 schema:givenName Oleg V.
97 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01023575604.49
98 rdf:type schema:Person
99 sg:person.010322665326.29 schema:affiliation https://www.grid.ac/institutes/grid.464621.3
100 schema:familyName Bogza
101 schema:givenName Sergey L.
102 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010322665326.29
103 rdf:type schema:Person
104 sg:person.010722472163.16 schema:affiliation https://www.grid.ac/institutes/grid.493162.b
105 schema:familyName Mazepa
106 schema:givenName Alexander V.
107 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010722472163.16
108 rdf:type schema:Person
109 sg:person.014040034526.14 schema:affiliation N01214670c9ff4270944dda4f94133319
110 schema:familyName Tolkunov
111 schema:givenName Andrey S.
112 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014040034526.14
113 rdf:type schema:Person
114 sg:person.07525304726.05 schema:affiliation https://www.grid.ac/institutes/grid.464621.3
115 schema:familyName Sujkov
116 schema:givenName Sergey Yu.
117 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07525304726.05
118 rdf:type schema:Person
119 sg:pub.10.1007/s10593-010-0550-x schema:sameAs https://app.dimensions.ai/details/publication/pub.1014921473
120 https://doi.org/10.1007/s10593-010-0550-x
121 rdf:type schema:CreativeWork
122 sg:pub.10.1007/s10593-010-0573-3 schema:sameAs https://app.dimensions.ai/details/publication/pub.1025978009
123 https://doi.org/10.1007/s10593-010-0573-3
124 rdf:type schema:CreativeWork
125 https://app.dimensions.ai/details/publication/pub.1077007229 schema:CreativeWork
126 https://doi.org/10.1002/cber.19741071219 schema:sameAs https://app.dimensions.ai/details/publication/pub.1030617658
127 rdf:type schema:CreativeWork
128 https://doi.org/10.1002/cmdc.200600144 schema:sameAs https://app.dimensions.ai/details/publication/pub.1023004603
129 rdf:type schema:CreativeWork
130 https://doi.org/10.1016/0896-6273(93)90241-i schema:sameAs https://app.dimensions.ai/details/publication/pub.1039384809
131 rdf:type schema:CreativeWork
132 https://doi.org/10.1016/j.bmcl.2005.09.029 schema:sameAs https://app.dimensions.ai/details/publication/pub.1047267310
133 rdf:type schema:CreativeWork
134 https://doi.org/10.1016/s0014-827x(01)01186-7 schema:sameAs https://app.dimensions.ai/details/publication/pub.1030205664
135 rdf:type schema:CreativeWork
136 https://doi.org/10.1016/s0014-827x(99)00022-1 schema:sameAs https://app.dimensions.ai/details/publication/pub.1022172717
137 rdf:type schema:CreativeWork
138 https://doi.org/10.1016/s0040-4039(01)01602-1 schema:sameAs https://app.dimensions.ai/details/publication/pub.1034467725
139 rdf:type schema:CreativeWork
140 https://doi.org/10.1016/s0301-0082(99)00020-9 schema:sameAs https://app.dimensions.ai/details/publication/pub.1019401498
141 rdf:type schema:CreativeWork
142 https://doi.org/10.1016/s0960-894x(00)00693-4 schema:sameAs https://app.dimensions.ai/details/publication/pub.1043718235
143 rdf:type schema:CreativeWork
144 https://doi.org/10.1016/s0960-894x(98)00148-6 schema:sameAs https://app.dimensions.ai/details/publication/pub.1043107171
145 rdf:type schema:CreativeWork
146 https://doi.org/10.1016/s0968-0896(00)00133-4 schema:sameAs https://app.dimensions.ai/details/publication/pub.1021152352
147 rdf:type schema:CreativeWork
148 https://doi.org/10.1021/jm001012y schema:sameAs https://app.dimensions.ai/details/publication/pub.1016415703
149 rdf:type schema:CreativeWork
150 https://doi.org/10.1021/jm030821p schema:sameAs https://app.dimensions.ai/details/publication/pub.1055948283
151 rdf:type schema:CreativeWork
152 https://doi.org/10.1021/jm050552y schema:sameAs https://app.dimensions.ai/details/publication/pub.1055949680
153 rdf:type schema:CreativeWork
154 https://doi.org/10.1021/jm0580003 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055950073
155 rdf:type schema:CreativeWork
156 https://doi.org/10.1021/jm960506l schema:sameAs https://app.dimensions.ai/details/publication/pub.1055957815
157 rdf:type schema:CreativeWork
158 https://doi.org/10.1021/jm980168j schema:sameAs https://app.dimensions.ai/details/publication/pub.1055958807
159 rdf:type schema:CreativeWork
160 https://doi.org/10.1039/p19840000849 schema:sameAs https://app.dimensions.ai/details/publication/pub.1040384628
161 rdf:type schema:CreativeWork
162 https://doi.org/10.1107/s0108767307043930 schema:sameAs https://app.dimensions.ai/details/publication/pub.1027786902
163 rdf:type schema:CreativeWork
164 https://doi.org/10.1358/dof.2001.026.08.630957 schema:sameAs https://app.dimensions.ai/details/publication/pub.1065061504
165 rdf:type schema:CreativeWork
166 https://doi.org/10.3987/com-99-8487 schema:sameAs https://app.dimensions.ai/details/publication/pub.1071774297
167 rdf:type schema:CreativeWork
168 https://www.grid.ac/institutes/grid.18999.30 schema:alternateName University of Kharkiv
169 schema:name SSI “Institute for Single Crystals”, 60 Nauky ave., 61001, Kharkiv, Ukraine
170 V. N. Karazin Kharkiv National University, 4 Svobody Sq., 61022, Kharkiv, Ukraine
171 rdf:type schema:Organization
172 https://www.grid.ac/institutes/grid.464621.3 schema:alternateName Institute of Organic Chemistry
173 schema:name Institute of Organic Chemistry, 5 Murmanska Str., 02660, Kiev, Ukraine
174 rdf:type schema:Organization
175 https://www.grid.ac/institutes/grid.493162.b schema:alternateName Physical-Chemical Institute O. Bogatsky
176 schema:name A.V. Bogatsky Physico-Chemical Institute, 86 Lustdorfska Str., 65080, Odessa, Ukraine
177 rdf:type schema:Organization
 




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


...