Annulation of tetrahydro-2-pyrimidinone with α-iodo ketones View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2018-05

AUTHORS

Ivan А. Dorofeev, Ludmila G. Shagun, Larisa V. Zhilitskaya, Nina O. Yarosh, Ludmila I. Larina

ABSTRACT

The first annulated heterocyclic derivatives of tetrahydro-2-pyrimidin-2(1H)-one were synthesized in one preparative step on the basis of a solventless three-component reaction of tetrahydro-2-pyrimidin-2(1H)-one with 1-iodopropan-2-one, 2-iodo-1-phenylethan-1-one, 2-iodo-1-(thiophen-2-yl)ethan-1-one, or 1,3-diiodopropan-2-one and elemental iodine in the absence of a base.

PAGES

550-553

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-018-2302-2

DOI

http://dx.doi.org/10.1007/s10593-018-2302-2

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1105221496


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": "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 of the Russian Academy of Sciences, 1 Favorsky St., 664033, Irkutsk, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Dorofeev", 
        "givenName": "Ivan \u0410.", 
        "id": "sg:person.014611446366.26", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014611446366.26"
        ], 
        "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 of the Russian Academy of Sciences, 1 Favorsky St., 664033, Irkutsk, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Shagun", 
        "givenName": "Ludmila G.", 
        "id": "sg:person.010246711775.43", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010246711775.43"
        ], 
        "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 of the Russian Academy of Sciences, 1 Favorsky St., 664033, Irkutsk, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Zhilitskaya", 
        "givenName": "Larisa V.", 
        "id": "sg:person.014543333166.51", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014543333166.51"
        ], 
        "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 of the Russian Academy of Sciences, 1 Favorsky St., 664033, Irkutsk, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Yarosh", 
        "givenName": "Nina O.", 
        "id": "sg:person.013747776412.80", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013747776412.80"
        ], 
        "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 of the Russian Academy of Sciences, 1 Favorsky St., 664033, Irkutsk, Russia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Larina", 
        "givenName": "Ludmila I.", 
        "id": "sg:person.07724760420.62", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07724760420.62"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "https://doi.org/10.1002/hc.20508", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1000277197"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1134/s106816201205007x", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1000996600", 
          "https://doi.org/10.1134/s106816201205007x"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.tet.2005.06.114", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1001324349"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s10593-017-1999-7", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1002856809", 
          "https://doi.org/10.1007/s10593-017-1999-7"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s10593-017-1999-7", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1002856809", 
          "https://doi.org/10.1007/s10593-017-1999-7"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1039/p29810000317", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1002878321"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ol052920y", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1010233717"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ol052920y", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1010233717"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1080/00397918808060741", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1018127972"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s11094-013-0920-7", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1024234869", 
          "https://doi.org/10.1007/s11094-013-0920-7"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/anie.201205233", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1028568502"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s0925-4439(02)00089-3", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1029795410"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.mencom.2015.09.004", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1031849877"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s10593-017-1986-z", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1032091832", 
          "https://doi.org/10.1007/s10593-017-1986-z"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s10593-017-1986-z", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1032091832", 
          "https://doi.org/10.1007/s10593-017-1986-z"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1039/jr9470000307", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1033363929"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/0022-328x(91)86160-r", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1035788798"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.bmcl.2004.08.038", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1035899052"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/prep.201300100", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1037818538"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/hlca.200590261", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1038930076"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/hlca.200590261", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1038930076"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ol060707b", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1047099637"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ol060707b", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1047099637"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.mencom.2016.07.032", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1049082309"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm00121a041", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055935881"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm0704705", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055951250"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm0704705", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055951250"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jo00052a060", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055963488"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jo0109319", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056003610"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jo0109319", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056003610"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ol990690f", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056260738"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ol990690f", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1056260738"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1055/s-1982-29837", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1057389894"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1524/ract.2006.94.9-11.739", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1067647574"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1134/s1070428017030162", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1085134108", 
          "https://doi.org/10.1134/s1070428017030162"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1134/s1070428017040248", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1085738165", 
          "https://doi.org/10.1134/s1070428017040248"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s10593-017-2146-1", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1092060350", 
          "https://doi.org/10.1007/s10593-017-2146-1"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1070/rcr4763", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1092463469"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2018-05", 
    "datePublishedReg": "2018-05-01", 
    "description": "The first annulated heterocyclic derivatives of tetrahydro-2-pyrimidin-2(1H)-one were synthesized in one preparative step on the basis of a solventless three-component reaction of tetrahydro-2-pyrimidin-2(1H)-one with 1-iodopropan-2-one, 2-iodo-1-phenylethan-1-one, 2-iodo-1-(thiophen-2-yl)ethan-1-one, or 1,3-diiodopropan-2-one and elemental iodine in the absence of a base.", 
    "genre": "research_article", 
    "id": "sg:pub.10.1007/s10593-018-2302-2", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1356886", 
        "issn": [
          "0009-3122", 
          "1573-8353"
        ], 
        "name": "Chemistry of Heterocyclic Compounds", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "5", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "54"
      }
    ], 
    "name": "Annulation of tetrahydro-2-pyrimidinone with \u03b1-iodo ketones", 
    "pagination": "550-553", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "ebb613b4fb401d54c375d7fa0a422c7c091c5d8b5eebb2f16937f390254a6525"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s10593-018-2302-2"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1105221496"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s10593-018-2302-2", 
      "https://app.dimensions.ai/details/publication/pub.1105221496"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-11T01:15", 
    "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_8697_00000557.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://link.springer.com/10.1007%2Fs10593-018-2302-2"
  }
]
 

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/s10593-018-2302-2'

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/s10593-018-2302-2'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s10593-018-2302-2'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s10593-018-2302-2'


 

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

186 TRIPLES      21 PREDICATES      57 URIs      19 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s10593-018-2302-2 schema:about anzsrc-for:03
2 anzsrc-for:0305
3 schema:author N9016806ccf2d4a3a9a4e9d597c982afd
4 schema:citation sg:pub.10.1007/s10593-017-1986-z
5 sg:pub.10.1007/s10593-017-1999-7
6 sg:pub.10.1007/s10593-017-2146-1
7 sg:pub.10.1007/s11094-013-0920-7
8 sg:pub.10.1134/s106816201205007x
9 sg:pub.10.1134/s1070428017030162
10 sg:pub.10.1134/s1070428017040248
11 https://doi.org/10.1002/anie.201205233
12 https://doi.org/10.1002/hc.20508
13 https://doi.org/10.1002/hlca.200590261
14 https://doi.org/10.1002/prep.201300100
15 https://doi.org/10.1016/0022-328x(91)86160-r
16 https://doi.org/10.1016/j.bmcl.2004.08.038
17 https://doi.org/10.1016/j.mencom.2015.09.004
18 https://doi.org/10.1016/j.mencom.2016.07.032
19 https://doi.org/10.1016/j.tet.2005.06.114
20 https://doi.org/10.1016/s0925-4439(02)00089-3
21 https://doi.org/10.1021/jm00121a041
22 https://doi.org/10.1021/jm0704705
23 https://doi.org/10.1021/jo00052a060
24 https://doi.org/10.1021/jo0109319
25 https://doi.org/10.1021/ol052920y
26 https://doi.org/10.1021/ol060707b
27 https://doi.org/10.1021/ol990690f
28 https://doi.org/10.1039/jr9470000307
29 https://doi.org/10.1039/p29810000317
30 https://doi.org/10.1055/s-1982-29837
31 https://doi.org/10.1070/rcr4763
32 https://doi.org/10.1080/00397918808060741
33 https://doi.org/10.1524/ract.2006.94.9-11.739
34 schema:datePublished 2018-05
35 schema:datePublishedReg 2018-05-01
36 schema:description The first annulated heterocyclic derivatives of tetrahydro-2-pyrimidin-2(1H)-one were synthesized in one preparative step on the basis of a solventless three-component reaction of tetrahydro-2-pyrimidin-2(1H)-one with 1-iodopropan-2-one, 2-iodo-1-phenylethan-1-one, 2-iodo-1-(thiophen-2-yl)ethan-1-one, or 1,3-diiodopropan-2-one and elemental iodine in the absence of a base.
37 schema:genre research_article
38 schema:inLanguage en
39 schema:isAccessibleForFree false
40 schema:isPartOf Naadf0e59859749f482d0d515281548c7
41 Nce3833a9b397490280c99a7c22e38cbc
42 sg:journal.1356886
43 schema:name Annulation of tetrahydro-2-pyrimidinone with α-iodo ketones
44 schema:pagination 550-553
45 schema:productId N56dfffeeca28450da87fe68b0f0467c1
46 N711c1c571e324bdd877f91978d9fb2fd
47 Nfa1b4ef397c54367a51a00c4b0591bd3
48 schema:sameAs https://app.dimensions.ai/details/publication/pub.1105221496
49 https://doi.org/10.1007/s10593-018-2302-2
50 schema:sdDatePublished 2019-04-11T01:15
51 schema:sdLicense https://scigraph.springernature.com/explorer/license/
52 schema:sdPublisher Nd60ba70654734758bfe1bba31876bcf7
53 schema:url https://link.springer.com/10.1007%2Fs10593-018-2302-2
54 sgo:license sg:explorer/license/
55 sgo:sdDataset articles
56 rdf:type schema:ScholarlyArticle
57 N32e1586eb6c94507b1bafae45e9d635a rdf:first sg:person.07724760420.62
58 rdf:rest rdf:nil
59 N4757a76ac77c4571b714b7b77d097aba rdf:first sg:person.013747776412.80
60 rdf:rest N32e1586eb6c94507b1bafae45e9d635a
61 N4e9cad29153c4ee98180802641485023 rdf:first sg:person.010246711775.43
62 rdf:rest Nd5c4eb3b152846239e4cea905d1cc1f7
63 N56dfffeeca28450da87fe68b0f0467c1 schema:name doi
64 schema:value 10.1007/s10593-018-2302-2
65 rdf:type schema:PropertyValue
66 N711c1c571e324bdd877f91978d9fb2fd schema:name readcube_id
67 schema:value ebb613b4fb401d54c375d7fa0a422c7c091c5d8b5eebb2f16937f390254a6525
68 rdf:type schema:PropertyValue
69 N9016806ccf2d4a3a9a4e9d597c982afd rdf:first sg:person.014611446366.26
70 rdf:rest N4e9cad29153c4ee98180802641485023
71 Naadf0e59859749f482d0d515281548c7 schema:volumeNumber 54
72 rdf:type schema:PublicationVolume
73 Nce3833a9b397490280c99a7c22e38cbc schema:issueNumber 5
74 rdf:type schema:PublicationIssue
75 Nd5c4eb3b152846239e4cea905d1cc1f7 rdf:first sg:person.014543333166.51
76 rdf:rest N4757a76ac77c4571b714b7b77d097aba
77 Nd60ba70654734758bfe1bba31876bcf7 schema:name Springer Nature - SN SciGraph project
78 rdf:type schema:Organization
79 Nfa1b4ef397c54367a51a00c4b0591bd3 schema:name dimensions_id
80 schema:value pub.1105221496
81 rdf:type schema:PropertyValue
82 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
83 schema:name Chemical Sciences
84 rdf:type schema:DefinedTerm
85 anzsrc-for:0305 schema:inDefinedTermSet anzsrc-for:
86 schema:name Organic Chemistry
87 rdf:type schema:DefinedTerm
88 sg:journal.1356886 schema:issn 0009-3122
89 1573-8353
90 schema:name Chemistry of Heterocyclic Compounds
91 rdf:type schema:Periodical
92 sg:person.010246711775.43 schema:affiliation https://www.grid.ac/institutes/grid.465341.1
93 schema:familyName Shagun
94 schema:givenName Ludmila G.
95 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.010246711775.43
96 rdf:type schema:Person
97 sg:person.013747776412.80 schema:affiliation https://www.grid.ac/institutes/grid.465341.1
98 schema:familyName Yarosh
99 schema:givenName Nina O.
100 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013747776412.80
101 rdf:type schema:Person
102 sg:person.014543333166.51 schema:affiliation https://www.grid.ac/institutes/grid.465341.1
103 schema:familyName Zhilitskaya
104 schema:givenName Larisa V.
105 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014543333166.51
106 rdf:type schema:Person
107 sg:person.014611446366.26 schema:affiliation https://www.grid.ac/institutes/grid.465341.1
108 schema:familyName Dorofeev
109 schema:givenName Ivan А.
110 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.014611446366.26
111 rdf:type schema:Person
112 sg:person.07724760420.62 schema:affiliation https://www.grid.ac/institutes/grid.465341.1
113 schema:familyName Larina
114 schema:givenName Ludmila I.
115 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07724760420.62
116 rdf:type schema:Person
117 sg:pub.10.1007/s10593-017-1986-z schema:sameAs https://app.dimensions.ai/details/publication/pub.1032091832
118 https://doi.org/10.1007/s10593-017-1986-z
119 rdf:type schema:CreativeWork
120 sg:pub.10.1007/s10593-017-1999-7 schema:sameAs https://app.dimensions.ai/details/publication/pub.1002856809
121 https://doi.org/10.1007/s10593-017-1999-7
122 rdf:type schema:CreativeWork
123 sg:pub.10.1007/s10593-017-2146-1 schema:sameAs https://app.dimensions.ai/details/publication/pub.1092060350
124 https://doi.org/10.1007/s10593-017-2146-1
125 rdf:type schema:CreativeWork
126 sg:pub.10.1007/s11094-013-0920-7 schema:sameAs https://app.dimensions.ai/details/publication/pub.1024234869
127 https://doi.org/10.1007/s11094-013-0920-7
128 rdf:type schema:CreativeWork
129 sg:pub.10.1134/s106816201205007x schema:sameAs https://app.dimensions.ai/details/publication/pub.1000996600
130 https://doi.org/10.1134/s106816201205007x
131 rdf:type schema:CreativeWork
132 sg:pub.10.1134/s1070428017030162 schema:sameAs https://app.dimensions.ai/details/publication/pub.1085134108
133 https://doi.org/10.1134/s1070428017030162
134 rdf:type schema:CreativeWork
135 sg:pub.10.1134/s1070428017040248 schema:sameAs https://app.dimensions.ai/details/publication/pub.1085738165
136 https://doi.org/10.1134/s1070428017040248
137 rdf:type schema:CreativeWork
138 https://doi.org/10.1002/anie.201205233 schema:sameAs https://app.dimensions.ai/details/publication/pub.1028568502
139 rdf:type schema:CreativeWork
140 https://doi.org/10.1002/hc.20508 schema:sameAs https://app.dimensions.ai/details/publication/pub.1000277197
141 rdf:type schema:CreativeWork
142 https://doi.org/10.1002/hlca.200590261 schema:sameAs https://app.dimensions.ai/details/publication/pub.1038930076
143 rdf:type schema:CreativeWork
144 https://doi.org/10.1002/prep.201300100 schema:sameAs https://app.dimensions.ai/details/publication/pub.1037818538
145 rdf:type schema:CreativeWork
146 https://doi.org/10.1016/0022-328x(91)86160-r schema:sameAs https://app.dimensions.ai/details/publication/pub.1035788798
147 rdf:type schema:CreativeWork
148 https://doi.org/10.1016/j.bmcl.2004.08.038 schema:sameAs https://app.dimensions.ai/details/publication/pub.1035899052
149 rdf:type schema:CreativeWork
150 https://doi.org/10.1016/j.mencom.2015.09.004 schema:sameAs https://app.dimensions.ai/details/publication/pub.1031849877
151 rdf:type schema:CreativeWork
152 https://doi.org/10.1016/j.mencom.2016.07.032 schema:sameAs https://app.dimensions.ai/details/publication/pub.1049082309
153 rdf:type schema:CreativeWork
154 https://doi.org/10.1016/j.tet.2005.06.114 schema:sameAs https://app.dimensions.ai/details/publication/pub.1001324349
155 rdf:type schema:CreativeWork
156 https://doi.org/10.1016/s0925-4439(02)00089-3 schema:sameAs https://app.dimensions.ai/details/publication/pub.1029795410
157 rdf:type schema:CreativeWork
158 https://doi.org/10.1021/jm00121a041 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055935881
159 rdf:type schema:CreativeWork
160 https://doi.org/10.1021/jm0704705 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055951250
161 rdf:type schema:CreativeWork
162 https://doi.org/10.1021/jo00052a060 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055963488
163 rdf:type schema:CreativeWork
164 https://doi.org/10.1021/jo0109319 schema:sameAs https://app.dimensions.ai/details/publication/pub.1056003610
165 rdf:type schema:CreativeWork
166 https://doi.org/10.1021/ol052920y schema:sameAs https://app.dimensions.ai/details/publication/pub.1010233717
167 rdf:type schema:CreativeWork
168 https://doi.org/10.1021/ol060707b schema:sameAs https://app.dimensions.ai/details/publication/pub.1047099637
169 rdf:type schema:CreativeWork
170 https://doi.org/10.1021/ol990690f schema:sameAs https://app.dimensions.ai/details/publication/pub.1056260738
171 rdf:type schema:CreativeWork
172 https://doi.org/10.1039/jr9470000307 schema:sameAs https://app.dimensions.ai/details/publication/pub.1033363929
173 rdf:type schema:CreativeWork
174 https://doi.org/10.1039/p29810000317 schema:sameAs https://app.dimensions.ai/details/publication/pub.1002878321
175 rdf:type schema:CreativeWork
176 https://doi.org/10.1055/s-1982-29837 schema:sameAs https://app.dimensions.ai/details/publication/pub.1057389894
177 rdf:type schema:CreativeWork
178 https://doi.org/10.1070/rcr4763 schema:sameAs https://app.dimensions.ai/details/publication/pub.1092463469
179 rdf:type schema:CreativeWork
180 https://doi.org/10.1080/00397918808060741 schema:sameAs https://app.dimensions.ai/details/publication/pub.1018127972
181 rdf:type schema:CreativeWork
182 https://doi.org/10.1524/ract.2006.94.9-11.739 schema:sameAs https://app.dimensions.ai/details/publication/pub.1067647574
183 rdf:type schema:CreativeWork
184 https://www.grid.ac/institutes/grid.465341.1 schema:alternateName A.E. Favorsky Irkutsk Institute of Chemistry
185 schema:name A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky St., 664033, Irkutsk, Russia
186 rdf:type schema:Organization
 




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


...