Synthesis of new 1,5-diaryl-3-(arylamino)-1H-pyrrol-2(5H)-ones under catalyst-free and solvent-free conditions View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2014-02

AUTHORS

Khodabakhsh Niknam, Sanaz Mojikhalifeh

ABSTRACT

Several new 1,5-diaryl-3-(arylamino)-1H-pyrrol-2(5H)-ones were synthesized via the three-component condensation reaction of aldehydes, aromatic amines, and ethyl pyruvate under catalyst-free and solvent-free conditions. Also, 5-(4-hydroxyl-3-nitrophenyl)-1-(4-methoxy-phenyl)-3-(4-methoxyphenylamino)-1,5-dihydro-pyrrol-2-one was synthesized using oxime instead of aldehyde. The eco-friendly, simple procedure, green procedure, catalyst-free and solvent-free conditions, short reaction times, and high yields of the products are the advantages of this method. More... »

PAGES

111-117

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11030-013-9496-0

DOI

http://dx.doi.org/10.1007/s11030-013-9496-0

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1008673722

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/24357192


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"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Aldehydes", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Amines", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Chemistry Techniques, Synthetic", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Pyrroles", 
        "type": "DefinedTerm"
      }, 
      {
        "inDefinedTermSet": "https://www.nlm.nih.gov/mesh/", 
        "name": "Pyruvates", 
        "type": "DefinedTerm"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "Persian Gulf University", 
          "id": "https://www.grid.ac/institutes/grid.412491.b", 
          "name": [
            "Department of Chemistry, Faculty of Sciences, Persian Gulf University, 75169, Bushehr, Iran"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Niknam", 
        "givenName": "Khodabakhsh", 
        "id": "sg:person.01277600267.81", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01277600267.81"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Persian Gulf University", 
          "id": "https://www.grid.ac/institutes/grid.412491.b", 
          "name": [
            "Department of Chemistry, Faculty of Sciences, Persian Gulf University, 75169, Bushehr, Iran"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Mojikhalifeh", 
        "givenName": "Sanaz", 
        "id": "sg:person.0643157062.95", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0643157062.95"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "https://doi.org/10.1016/j.tetlet.2009.04.096", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1001281199"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/ejoc.200800249", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1003871233"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570430421", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1005074853"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570430421", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1005074853"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/0223-5234(91)90102-s", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1007221106"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s1872-2067(12)60532-4", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1008985607"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.tetlet.2009.06.140", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1009434447"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/cjoc.201180323", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1012713795"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s11164-012-0749-9", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1022735837", 
          "https://doi.org/10.1007/s11164-012-0749-9"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/ejoc.200600092", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1025298547"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s1872-2067(11)60421-x", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1025519211"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/s1872-2067(11)60457-9", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1027021219"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/bf00819965", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1043084773", 
          "https://doi.org/10.1007/bf00819965"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/bf00819965", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1043084773", 
          "https://doi.org/10.1007/bf00819965"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s00706-012-0910-6", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1051087142", 
          "https://doi.org/10.1007/s00706-012-0910-6"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570410306", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1051384856"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570410306", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1051384856"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.tetlet.2011.06.105", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1051766623"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/cr020100i", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1054030332"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/cr020100i", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1054030332"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/ja01501a064", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055802314"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm031089x", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055948440"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm031089x", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055948440"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://app.dimensions.ai/details/publication/pub.1082822303", 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2014-02", 
    "datePublishedReg": "2014-02-01", 
    "description": "Several new 1,5-diaryl-3-(arylamino)-1H-pyrrol-2(5H)-ones were synthesized via the three-component condensation reaction of aldehydes, aromatic amines, and ethyl pyruvate under catalyst-free and solvent-free conditions. Also, 5-(4-hydroxyl-3-nitrophenyl)-1-(4-methoxy-phenyl)-3-(4-methoxyphenylamino)-1,5-dihydro-pyrrol-2-one was synthesized using oxime instead of aldehyde. The eco-friendly, simple procedure, green procedure, catalyst-free and solvent-free conditions, short reaction times, and high yields of the products are the advantages of this method. ", 
    "genre": "research_article", 
    "id": "sg:pub.10.1007/s11030-013-9496-0", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1114785", 
        "issn": [
          "1381-1991", 
          "1573-501X"
        ], 
        "name": "Molecular Diversity", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "1", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "18"
      }
    ], 
    "name": "Synthesis of new 1,5-diaryl-3-(arylamino)-1H-pyrrol-2(5H)-ones under catalyst-free and solvent-free conditions", 
    "pagination": "111-117", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "2952d08316e94d551ae894f3f35a4e45c100c01c6b9c2c8c6fba5a4e5dea2e16"
        ]
      }, 
      {
        "name": "pubmed_id", 
        "type": "PropertyValue", 
        "value": [
          "24357192"
        ]
      }, 
      {
        "name": "nlm_unique_id", 
        "type": "PropertyValue", 
        "value": [
          "9516534"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s11030-013-9496-0"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1008673722"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s11030-013-9496-0", 
      "https://app.dimensions.ai/details/publication/pub.1008673722"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-10T21:36", 
    "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_8687_00000510.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "http://link.springer.com/10.1007%2Fs11030-013-9496-0"
  }
]
 

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/s11030-013-9496-0'

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/s11030-013-9496-0'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s11030-013-9496-0'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s11030-013-9496-0'


 

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

155 TRIPLES      21 PREDICATES      53 URIs      26 LITERALS      14 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s11030-013-9496-0 schema:about N65e82ed86a23464c82cf49cd54dadec9
2 N7601e4b5397d467f846665ab433944ba
3 Nabbf94629f1945078befdff2d6fd26b3
4 Ne0cfebd32c2a4475a9600dd25c2ec42d
5 Nf1f24bd757ac4a6eaf5330bbdbd8556c
6 anzsrc-for:03
7 anzsrc-for:0306
8 schema:author N1b856c1197c84f54b56fd46684b864af
9 schema:citation sg:pub.10.1007/bf00819965
10 sg:pub.10.1007/s00706-012-0910-6
11 sg:pub.10.1007/s11164-012-0749-9
12 https://app.dimensions.ai/details/publication/pub.1082822303
13 https://doi.org/10.1002/cjoc.201180323
14 https://doi.org/10.1002/ejoc.200600092
15 https://doi.org/10.1002/ejoc.200800249
16 https://doi.org/10.1002/jhet.5570410306
17 https://doi.org/10.1002/jhet.5570430421
18 https://doi.org/10.1016/0223-5234(91)90102-s
19 https://doi.org/10.1016/j.tetlet.2009.04.096
20 https://doi.org/10.1016/j.tetlet.2009.06.140
21 https://doi.org/10.1016/j.tetlet.2011.06.105
22 https://doi.org/10.1016/s1872-2067(11)60421-x
23 https://doi.org/10.1016/s1872-2067(11)60457-9
24 https://doi.org/10.1016/s1872-2067(12)60532-4
25 https://doi.org/10.1021/cr020100i
26 https://doi.org/10.1021/ja01501a064
27 https://doi.org/10.1021/jm031089x
28 schema:datePublished 2014-02
29 schema:datePublishedReg 2014-02-01
30 schema:description Several new 1,5-diaryl-3-(arylamino)-1H-pyrrol-2(5H)-ones were synthesized via the three-component condensation reaction of aldehydes, aromatic amines, and ethyl pyruvate under catalyst-free and solvent-free conditions. Also, 5-(4-hydroxyl-3-nitrophenyl)-1-(4-methoxy-phenyl)-3-(4-methoxyphenylamino)-1,5-dihydro-pyrrol-2-one was synthesized using oxime instead of aldehyde. The eco-friendly, simple procedure, green procedure, catalyst-free and solvent-free conditions, short reaction times, and high yields of the products are the advantages of this method.
31 schema:genre research_article
32 schema:inLanguage en
33 schema:isAccessibleForFree false
34 schema:isPartOf N7d3275424f0648c9a8aa82c9d3f08315
35 Nb228fddc1516407393893093fd91f0b3
36 sg:journal.1114785
37 schema:name Synthesis of new 1,5-diaryl-3-(arylamino)-1H-pyrrol-2(5H)-ones under catalyst-free and solvent-free conditions
38 schema:pagination 111-117
39 schema:productId N49b1178b8a5e489e917dc5b4ac669f1d
40 N53a485fc2e3844a0b348e321719eedc4
41 N6b5c368536544e8b9e75f5999411dfe6
42 Nae5e844bf9ad48a8b5b73ed7ab3bb7b5
43 Nf8f9c46023674abfa8bc3b962629b816
44 schema:sameAs https://app.dimensions.ai/details/publication/pub.1008673722
45 https://doi.org/10.1007/s11030-013-9496-0
46 schema:sdDatePublished 2019-04-10T21:36
47 schema:sdLicense https://scigraph.springernature.com/explorer/license/
48 schema:sdPublisher N8c1c4118dd2b48cfb7c0e3dfb0329ab9
49 schema:url http://link.springer.com/10.1007%2Fs11030-013-9496-0
50 sgo:license sg:explorer/license/
51 sgo:sdDataset articles
52 rdf:type schema:ScholarlyArticle
53 N1b856c1197c84f54b56fd46684b864af rdf:first sg:person.01277600267.81
54 rdf:rest N2d8c06206cf341759dd0840044552ff9
55 N2d8c06206cf341759dd0840044552ff9 rdf:first sg:person.0643157062.95
56 rdf:rest rdf:nil
57 N49b1178b8a5e489e917dc5b4ac669f1d schema:name dimensions_id
58 schema:value pub.1008673722
59 rdf:type schema:PropertyValue
60 N53a485fc2e3844a0b348e321719eedc4 schema:name doi
61 schema:value 10.1007/s11030-013-9496-0
62 rdf:type schema:PropertyValue
63 N65e82ed86a23464c82cf49cd54dadec9 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
64 schema:name Aldehydes
65 rdf:type schema:DefinedTerm
66 N6b5c368536544e8b9e75f5999411dfe6 schema:name nlm_unique_id
67 schema:value 9516534
68 rdf:type schema:PropertyValue
69 N7601e4b5397d467f846665ab433944ba schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
70 schema:name Amines
71 rdf:type schema:DefinedTerm
72 N7d3275424f0648c9a8aa82c9d3f08315 schema:issueNumber 1
73 rdf:type schema:PublicationIssue
74 N8c1c4118dd2b48cfb7c0e3dfb0329ab9 schema:name Springer Nature - SN SciGraph project
75 rdf:type schema:Organization
76 Nabbf94629f1945078befdff2d6fd26b3 schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
77 schema:name Pyrroles
78 rdf:type schema:DefinedTerm
79 Nae5e844bf9ad48a8b5b73ed7ab3bb7b5 schema:name readcube_id
80 schema:value 2952d08316e94d551ae894f3f35a4e45c100c01c6b9c2c8c6fba5a4e5dea2e16
81 rdf:type schema:PropertyValue
82 Nb228fddc1516407393893093fd91f0b3 schema:volumeNumber 18
83 rdf:type schema:PublicationVolume
84 Ne0cfebd32c2a4475a9600dd25c2ec42d schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
85 schema:name Pyruvates
86 rdf:type schema:DefinedTerm
87 Nf1f24bd757ac4a6eaf5330bbdbd8556c schema:inDefinedTermSet https://www.nlm.nih.gov/mesh/
88 schema:name Chemistry Techniques, Synthetic
89 rdf:type schema:DefinedTerm
90 Nf8f9c46023674abfa8bc3b962629b816 schema:name pubmed_id
91 schema:value 24357192
92 rdf:type schema:PropertyValue
93 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
94 schema:name Chemical Sciences
95 rdf:type schema:DefinedTerm
96 anzsrc-for:0306 schema:inDefinedTermSet anzsrc-for:
97 schema:name Physical Chemistry (incl. Structural)
98 rdf:type schema:DefinedTerm
99 sg:journal.1114785 schema:issn 1381-1991
100 1573-501X
101 schema:name Molecular Diversity
102 rdf:type schema:Periodical
103 sg:person.01277600267.81 schema:affiliation https://www.grid.ac/institutes/grid.412491.b
104 schema:familyName Niknam
105 schema:givenName Khodabakhsh
106 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01277600267.81
107 rdf:type schema:Person
108 sg:person.0643157062.95 schema:affiliation https://www.grid.ac/institutes/grid.412491.b
109 schema:familyName Mojikhalifeh
110 schema:givenName Sanaz
111 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0643157062.95
112 rdf:type schema:Person
113 sg:pub.10.1007/bf00819965 schema:sameAs https://app.dimensions.ai/details/publication/pub.1043084773
114 https://doi.org/10.1007/bf00819965
115 rdf:type schema:CreativeWork
116 sg:pub.10.1007/s00706-012-0910-6 schema:sameAs https://app.dimensions.ai/details/publication/pub.1051087142
117 https://doi.org/10.1007/s00706-012-0910-6
118 rdf:type schema:CreativeWork
119 sg:pub.10.1007/s11164-012-0749-9 schema:sameAs https://app.dimensions.ai/details/publication/pub.1022735837
120 https://doi.org/10.1007/s11164-012-0749-9
121 rdf:type schema:CreativeWork
122 https://app.dimensions.ai/details/publication/pub.1082822303 schema:CreativeWork
123 https://doi.org/10.1002/cjoc.201180323 schema:sameAs https://app.dimensions.ai/details/publication/pub.1012713795
124 rdf:type schema:CreativeWork
125 https://doi.org/10.1002/ejoc.200600092 schema:sameAs https://app.dimensions.ai/details/publication/pub.1025298547
126 rdf:type schema:CreativeWork
127 https://doi.org/10.1002/ejoc.200800249 schema:sameAs https://app.dimensions.ai/details/publication/pub.1003871233
128 rdf:type schema:CreativeWork
129 https://doi.org/10.1002/jhet.5570410306 schema:sameAs https://app.dimensions.ai/details/publication/pub.1051384856
130 rdf:type schema:CreativeWork
131 https://doi.org/10.1002/jhet.5570430421 schema:sameAs https://app.dimensions.ai/details/publication/pub.1005074853
132 rdf:type schema:CreativeWork
133 https://doi.org/10.1016/0223-5234(91)90102-s schema:sameAs https://app.dimensions.ai/details/publication/pub.1007221106
134 rdf:type schema:CreativeWork
135 https://doi.org/10.1016/j.tetlet.2009.04.096 schema:sameAs https://app.dimensions.ai/details/publication/pub.1001281199
136 rdf:type schema:CreativeWork
137 https://doi.org/10.1016/j.tetlet.2009.06.140 schema:sameAs https://app.dimensions.ai/details/publication/pub.1009434447
138 rdf:type schema:CreativeWork
139 https://doi.org/10.1016/j.tetlet.2011.06.105 schema:sameAs https://app.dimensions.ai/details/publication/pub.1051766623
140 rdf:type schema:CreativeWork
141 https://doi.org/10.1016/s1872-2067(11)60421-x schema:sameAs https://app.dimensions.ai/details/publication/pub.1025519211
142 rdf:type schema:CreativeWork
143 https://doi.org/10.1016/s1872-2067(11)60457-9 schema:sameAs https://app.dimensions.ai/details/publication/pub.1027021219
144 rdf:type schema:CreativeWork
145 https://doi.org/10.1016/s1872-2067(12)60532-4 schema:sameAs https://app.dimensions.ai/details/publication/pub.1008985607
146 rdf:type schema:CreativeWork
147 https://doi.org/10.1021/cr020100i schema:sameAs https://app.dimensions.ai/details/publication/pub.1054030332
148 rdf:type schema:CreativeWork
149 https://doi.org/10.1021/ja01501a064 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055802314
150 rdf:type schema:CreativeWork
151 https://doi.org/10.1021/jm031089x schema:sameAs https://app.dimensions.ai/details/publication/pub.1055948440
152 rdf:type schema:CreativeWork
153 https://www.grid.ac/institutes/grid.412491.b schema:alternateName Persian Gulf University
154 schema:name Department of Chemistry, Faculty of Sciences, Persian Gulf University, 75169, Bushehr, Iran
155 rdf:type schema:Organization
 




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


...