Small-ring inclusion hosts. 4. X-ray crystal structures oftrans-3,3-Bis(4-methylphenyl)cyclopropane-1,2-dicarboxylic acid and of its inclusion complex with Dimethyl Sulphoxide (1:2) View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1992-06

AUTHORS

Ingeborg Csöregh, Olga Gallardo, Edwin Weber, Manfred Hecker, Andreas Wierig

ABSTRACT

The crystal structures of the unsolvatedtrans-3,3-bis(4-methylphenyl)cyclopropane-1,2-dicarboxylic acid (1) and of its inclusion compound with dimethyl sulphoxide,1·DMSO (1:2), have been studied by X-ray diffraction. Crystals of1 show triclinic symmetry (P) withZ = 4 and the unit cell dimensionsa = 7.617(2),b = 15.321(4),c = 15.297(3) Å,α = 109.76(2),β = 103.47(1),γ = 89.87(2)°. FinalR = 0.037 for 3601 reflections collected atT = 153(1) K. Crystals of1·DMSO (1: 2) are monoclinic (P21/n) withZ = 4 and cell dimensionsa = 10.744(1),b = 10.806(1),c = 21.302(2) Å,β = 101.68(1)°. The clathrate structure was refined toR = 0.034 for 1671 reflections obtained atT = 173(1) K. In the unsolvated host compound cyclic pairs of O-H ... bonds, commonly observed in carboxylic acids, couple the carboxylic functions two by two, thus giving rise to endless chains due to the bifunctionality and thetrans position of the acid groups of1. The complex with DMSO as guest, however, consists of distinct hydrogen-bonded 1:2 host-guest associates, held together by weak intermolecular interactions. More... »

PAGES

131-140

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf01029660

DOI

http://dx.doi.org/10.1007/bf01029660

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1006909977


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": {
          "alternateName": "Stockholm University", 
          "id": "https://www.grid.ac/institutes/grid.10548.38", 
          "name": [
            "Department of Structural Chemistry, Arrhenius Laboratory, Stockholm University, S-106 91, Stockholm, Sweden"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Cs\u00f6regh", 
        "givenName": "Ingeborg", 
        "id": "sg:person.015544624271.40", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015544624271.40"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Stockholm University", 
          "id": "https://www.grid.ac/institutes/grid.10548.38", 
          "name": [
            "Department of Structural Chemistry, Arrhenius Laboratory, Stockholm University, S-106 91, Stockholm, Sweden"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Gallardo", 
        "givenName": "Olga", 
        "id": "sg:person.013716237331.32", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013716237331.32"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "University of Bonn", 
          "id": "https://www.grid.ac/institutes/grid.10388.32", 
          "name": [
            "Institut f\u00fcr Organische Chemie und Biochemie der Universit\u00e4t Bonn, Gerhard-Domagk-Stra\u00dfe 1, D-5300, Bonn-1, Germany"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Weber", 
        "givenName": "Edwin", 
        "id": "sg:person.01016205541.34", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01016205541.34"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "University of Bonn", 
          "id": "https://www.grid.ac/institutes/grid.10388.32", 
          "name": [
            "Institut f\u00fcr Organische Chemie und Biochemie der Universit\u00e4t Bonn, Gerhard-Domagk-Stra\u00dfe 1, D-5300, Bonn-1, Germany"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Hecker", 
        "givenName": "Manfred", 
        "id": "sg:person.07461224345.87", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07461224345.87"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "University of Bonn", 
          "id": "https://www.grid.ac/institutes/grid.10388.32", 
          "name": [
            "Institut f\u00fcr Organische Chemie und Biochemie der Universit\u00e4t Bonn, Gerhard-Domagk-Stra\u00dfe 1, D-5300, Bonn-1, Germany"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Wierig", 
        "givenName": "Andreas", 
        "id": "sg:person.07605334477.35", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07605334477.35"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "https://doi.org/10.1107/s0108767390000277", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1010133616"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1107/s0567740876003968", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1012189855"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1246/bcsj.64.2539", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1013354727"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1039/p29860000507", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1014189202"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1039/p29920001939", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1015619463"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/0263-7855(89)80053-0", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1033151998"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1039/p29900000283", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1034612263"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/bf01041884", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1043246814", 
          "https://doi.org/10.1007/bf01041884"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1039/c39910001239", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1047186805"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ar00010a002", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055148223"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ar00127a005", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055149145"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ar00172a005", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055149454"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/cen-v064n029.p028", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055344588"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ed067p829", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055459217"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ja00202a030", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055713910"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ja00368a031", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055726940"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ja00383a012", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055728003"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jo00260a007", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055975918"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "1992-06", 
    "datePublishedReg": "1992-06-01", 
    "description": "The crystal structures of the unsolvatedtrans-3,3-bis(4-methylphenyl)cyclopropane-1,2-dicarboxylic acid (1) and of its inclusion compound with dimethyl sulphoxide,1\u00b7DMSO (1:2), have been studied by X-ray diffraction. Crystals of1 show triclinic symmetry (P) withZ = 4 and the unit cell dimensionsa = 7.617(2),b = 15.321(4),c = 15.297(3) \u00c5,\u03b1 = 109.76(2),\u03b2 = 103.47(1),\u03b3 = 89.87(2)\u00b0. FinalR = 0.037 for 3601 reflections collected atT = 153(1) K. Crystals of1\u00b7DMSO (1: 2) are monoclinic (P21/n) withZ = 4 and cell dimensionsa = 10.744(1),b = 10.806(1),c = 21.302(2) \u00c5,\u03b2 = 101.68(1)\u00b0. The clathrate structure was refined toR = 0.034 for 1671 reflections obtained atT = 173(1) K. In the unsolvated host compound cyclic pairs of O-H ... bonds, commonly observed in carboxylic acids, couple the carboxylic functions two by two, thus giving rise to endless chains due to the bifunctionality and thetrans position of the acid groups of1. The complex with DMSO as guest, however, consists of distinct hydrogen-bonded 1:2 host-guest associates, held together by weak intermolecular interactions.", 
    "genre": "research_article", 
    "id": "sg:pub.10.1007/bf01029660", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1119385", 
        "issn": [
          "1388-3127", 
          "2212-1765"
        ], 
        "name": "Journal of Inclusion Phenomena and Macrocyclic Chemistry", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "2", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "14"
      }
    ], 
    "name": "Small-ring inclusion hosts. 4. X-ray crystal structures oftrans-3,3-Bis(4-methylphenyl)cyclopropane-1,2-dicarboxylic acid and of its inclusion complex with Dimethyl Sulphoxide (1:2)", 
    "pagination": "131-140", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "20ea679887d0588f915e868f65d5d46e612f583683fe11faf47fc755d6fec3da"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/bf01029660"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1006909977"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/bf01029660", 
      "https://app.dimensions.ai/details/publication/pub.1006909977"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-11T13:34", 
    "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/v90/0000000370_0000000370/records_46772_00000000.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "http://link.springer.com/10.1007/BF01029660"
  }
]
 

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/bf01029660'

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/bf01029660'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf01029660'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf01029660'


 

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

147 TRIPLES      21 PREDICATES      45 URIs      19 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/bf01029660 schema:about anzsrc-for:03
2 anzsrc-for:0306
3 schema:author N200cfb0f454f424492d180ceffccc86e
4 schema:citation sg:pub.10.1007/bf01041884
5 https://doi.org/10.1016/0263-7855(89)80053-0
6 https://doi.org/10.1021/ar00010a002
7 https://doi.org/10.1021/ar00127a005
8 https://doi.org/10.1021/ar00172a005
9 https://doi.org/10.1021/cen-v064n029.p028
10 https://doi.org/10.1021/ed067p829
11 https://doi.org/10.1021/ja00202a030
12 https://doi.org/10.1021/ja00368a031
13 https://doi.org/10.1021/ja00383a012
14 https://doi.org/10.1021/jo00260a007
15 https://doi.org/10.1039/c39910001239
16 https://doi.org/10.1039/p29860000507
17 https://doi.org/10.1039/p29900000283
18 https://doi.org/10.1039/p29920001939
19 https://doi.org/10.1107/s0108767390000277
20 https://doi.org/10.1107/s0567740876003968
21 https://doi.org/10.1246/bcsj.64.2539
22 schema:datePublished 1992-06
23 schema:datePublishedReg 1992-06-01
24 schema:description The crystal structures of the unsolvatedtrans-3,3-bis(4-methylphenyl)cyclopropane-1,2-dicarboxylic acid (1) and of its inclusion compound with dimethyl sulphoxide,1·DMSO (1:2), have been studied by X-ray diffraction. Crystals of1 show triclinic symmetry (P) withZ = 4 and the unit cell dimensionsa = 7.617(2),b = 15.321(4),c = 15.297(3) Å,α = 109.76(2),β = 103.47(1),γ = 89.87(2)°. FinalR = 0.037 for 3601 reflections collected atT = 153(1) K. Crystals of1·DMSO (1: 2) are monoclinic (P21/n) withZ = 4 and cell dimensionsa = 10.744(1),b = 10.806(1),c = 21.302(2) Å,β = 101.68(1)°. The clathrate structure was refined toR = 0.034 for 1671 reflections obtained atT = 173(1) K. In the unsolvated host compound cyclic pairs of O-H ... bonds, commonly observed in carboxylic acids, couple the carboxylic functions two by two, thus giving rise to endless chains due to the bifunctionality and thetrans position of the acid groups of1. The complex with DMSO as guest, however, consists of distinct hydrogen-bonded 1:2 host-guest associates, held together by weak intermolecular interactions.
25 schema:genre research_article
26 schema:inLanguage en
27 schema:isAccessibleForFree false
28 schema:isPartOf N5d5c8973267f47b3ad574baf21b7cd86
29 Nc2873fc1a37c4704ab4370fcada53dd0
30 sg:journal.1119385
31 schema:name Small-ring inclusion hosts. 4. X-ray crystal structures oftrans-3,3-Bis(4-methylphenyl)cyclopropane-1,2-dicarboxylic acid and of its inclusion complex with Dimethyl Sulphoxide (1:2)
32 schema:pagination 131-140
33 schema:productId N60c47d3837a840e8b8788f56a5244e6b
34 Na19d04dd56254e2a8e007979cd9bf5ea
35 Nf64d758086a74f3db89796cd66fb6827
36 schema:sameAs https://app.dimensions.ai/details/publication/pub.1006909977
37 https://doi.org/10.1007/bf01029660
38 schema:sdDatePublished 2019-04-11T13:34
39 schema:sdLicense https://scigraph.springernature.com/explorer/license/
40 schema:sdPublisher N24ee1b65fc484828900a8c34b155ea3d
41 schema:url http://link.springer.com/10.1007/BF01029660
42 sgo:license sg:explorer/license/
43 sgo:sdDataset articles
44 rdf:type schema:ScholarlyArticle
45 N0075a32c29e04d14ab7699007af2187e rdf:first sg:person.01016205541.34
46 rdf:rest N442f63ccd8c44a9cbbac6986b83812fd
47 N1c8ecd7eb31b4c4cb71b7155ceed6b7d rdf:first sg:person.07605334477.35
48 rdf:rest rdf:nil
49 N200cfb0f454f424492d180ceffccc86e rdf:first sg:person.015544624271.40
50 rdf:rest N6af590c360df4243b78f428612d94ba7
51 N24ee1b65fc484828900a8c34b155ea3d schema:name Springer Nature - SN SciGraph project
52 rdf:type schema:Organization
53 N442f63ccd8c44a9cbbac6986b83812fd rdf:first sg:person.07461224345.87
54 rdf:rest N1c8ecd7eb31b4c4cb71b7155ceed6b7d
55 N5d5c8973267f47b3ad574baf21b7cd86 schema:issueNumber 2
56 rdf:type schema:PublicationIssue
57 N60c47d3837a840e8b8788f56a5244e6b schema:name readcube_id
58 schema:value 20ea679887d0588f915e868f65d5d46e612f583683fe11faf47fc755d6fec3da
59 rdf:type schema:PropertyValue
60 N6af590c360df4243b78f428612d94ba7 rdf:first sg:person.013716237331.32
61 rdf:rest N0075a32c29e04d14ab7699007af2187e
62 Na19d04dd56254e2a8e007979cd9bf5ea schema:name doi
63 schema:value 10.1007/bf01029660
64 rdf:type schema:PropertyValue
65 Nc2873fc1a37c4704ab4370fcada53dd0 schema:volumeNumber 14
66 rdf:type schema:PublicationVolume
67 Nf64d758086a74f3db89796cd66fb6827 schema:name dimensions_id
68 schema:value pub.1006909977
69 rdf:type schema:PropertyValue
70 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
71 schema:name Chemical Sciences
72 rdf:type schema:DefinedTerm
73 anzsrc-for:0306 schema:inDefinedTermSet anzsrc-for:
74 schema:name Physical Chemistry (incl. Structural)
75 rdf:type schema:DefinedTerm
76 sg:journal.1119385 schema:issn 1388-3127
77 2212-1765
78 schema:name Journal of Inclusion Phenomena and Macrocyclic Chemistry
79 rdf:type schema:Periodical
80 sg:person.01016205541.34 schema:affiliation https://www.grid.ac/institutes/grid.10388.32
81 schema:familyName Weber
82 schema:givenName Edwin
83 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01016205541.34
84 rdf:type schema:Person
85 sg:person.013716237331.32 schema:affiliation https://www.grid.ac/institutes/grid.10548.38
86 schema:familyName Gallardo
87 schema:givenName Olga
88 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013716237331.32
89 rdf:type schema:Person
90 sg:person.015544624271.40 schema:affiliation https://www.grid.ac/institutes/grid.10548.38
91 schema:familyName Csöregh
92 schema:givenName Ingeborg
93 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015544624271.40
94 rdf:type schema:Person
95 sg:person.07461224345.87 schema:affiliation https://www.grid.ac/institutes/grid.10388.32
96 schema:familyName Hecker
97 schema:givenName Manfred
98 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07461224345.87
99 rdf:type schema:Person
100 sg:person.07605334477.35 schema:affiliation https://www.grid.ac/institutes/grid.10388.32
101 schema:familyName Wierig
102 schema:givenName Andreas
103 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.07605334477.35
104 rdf:type schema:Person
105 sg:pub.10.1007/bf01041884 schema:sameAs https://app.dimensions.ai/details/publication/pub.1043246814
106 https://doi.org/10.1007/bf01041884
107 rdf:type schema:CreativeWork
108 https://doi.org/10.1016/0263-7855(89)80053-0 schema:sameAs https://app.dimensions.ai/details/publication/pub.1033151998
109 rdf:type schema:CreativeWork
110 https://doi.org/10.1021/ar00010a002 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055148223
111 rdf:type schema:CreativeWork
112 https://doi.org/10.1021/ar00127a005 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055149145
113 rdf:type schema:CreativeWork
114 https://doi.org/10.1021/ar00172a005 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055149454
115 rdf:type schema:CreativeWork
116 https://doi.org/10.1021/cen-v064n029.p028 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055344588
117 rdf:type schema:CreativeWork
118 https://doi.org/10.1021/ed067p829 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055459217
119 rdf:type schema:CreativeWork
120 https://doi.org/10.1021/ja00202a030 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055713910
121 rdf:type schema:CreativeWork
122 https://doi.org/10.1021/ja00368a031 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055726940
123 rdf:type schema:CreativeWork
124 https://doi.org/10.1021/ja00383a012 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055728003
125 rdf:type schema:CreativeWork
126 https://doi.org/10.1021/jo00260a007 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055975918
127 rdf:type schema:CreativeWork
128 https://doi.org/10.1039/c39910001239 schema:sameAs https://app.dimensions.ai/details/publication/pub.1047186805
129 rdf:type schema:CreativeWork
130 https://doi.org/10.1039/p29860000507 schema:sameAs https://app.dimensions.ai/details/publication/pub.1014189202
131 rdf:type schema:CreativeWork
132 https://doi.org/10.1039/p29900000283 schema:sameAs https://app.dimensions.ai/details/publication/pub.1034612263
133 rdf:type schema:CreativeWork
134 https://doi.org/10.1039/p29920001939 schema:sameAs https://app.dimensions.ai/details/publication/pub.1015619463
135 rdf:type schema:CreativeWork
136 https://doi.org/10.1107/s0108767390000277 schema:sameAs https://app.dimensions.ai/details/publication/pub.1010133616
137 rdf:type schema:CreativeWork
138 https://doi.org/10.1107/s0567740876003968 schema:sameAs https://app.dimensions.ai/details/publication/pub.1012189855
139 rdf:type schema:CreativeWork
140 https://doi.org/10.1246/bcsj.64.2539 schema:sameAs https://app.dimensions.ai/details/publication/pub.1013354727
141 rdf:type schema:CreativeWork
142 https://www.grid.ac/institutes/grid.10388.32 schema:alternateName University of Bonn
143 schema:name Institut für Organische Chemie und Biochemie der Universität Bonn, Gerhard-Domagk-Straße 1, D-5300, Bonn-1, Germany
144 rdf:type schema:Organization
145 https://www.grid.ac/institutes/grid.10548.38 schema:alternateName Stockholm University
146 schema:name Department of Structural Chemistry, Arrhenius Laboratory, Stockholm University, S-106 91, Stockholm, Sweden
147 rdf:type schema:Organization
 




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


...