Click 1,4-regioselective synthesis, characterization, and antimicrobial screening of novel 1,2,3-triazoles tethering fluorinated 1,2,4-triazole and lipophilic side chain View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2017-02

AUTHORS

Nadjet Rezki, Mariem Mohammed Mayaba, Fawzia Faleh Al-blewi, Mohamed Reda Aouad, El Sayed Helmi El Ashry

ABSTRACT

Base-catalyzed alkylation of 5-(4-fluorophenyl)-2,4-dihydro-1,2,4-triazole-3-thione (3) with one or two equivalents of propargyl bromide in presence of triethylamine as catalyst selectively produced the thiopropargylated 1,2,4-triazole 7 in 90 % yield. Under the same reaction conditions, 4-ethyl-5-(4-fluorophenyl)-3-(prop-2-yn-1-ylthio)-1,2,4-triazole (8) was produced. Conversely, when the propargylation was carried out in presence of sodium bicarbonate, a mixture of S,N4- (24) and S,N2-bis(propargylated) triazoles (25) was obtained in 85 % overall yield. The click 1,3-dipolar cycloaddition reaction of the mono- (7, 8) and/or bis(propargylated)-1,2,4-triazoles (24) with a variety of long-chain alkyl azides, conducted in t-BuOH:H2O (10:1) in presence of sodium ascorbate and copper(II) sulfate at room temperature, afforded the regioselective 1,4-disubstituted mono- (14–18) and bis(1,2,3-triazole) derivatives (26–30) containing a fluorinated 1,2,4-triazole moiety and a lipophilic side chain. The structures of the new products were elucidated by infrared (IR), 1H and 13C nuclear magnetic resonance (NMR), and mass spectrometry. They were also assessed in vitro for their antimicrobial potency against six bacteria (Bacillus subtilis, Streptococcus pneumonia, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumonia) and two fungi (Aspergillus fumigatus and Candida albicans). The bioassay results revealed that some of the tested compounds displayed promising antimicrobial activity. More... »

PAGES

995-1011

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11164-016-2679-4

DOI

http://dx.doi.org/10.1007/s11164-016-2679-4

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1043755371


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/2008/0601", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Biochemistry and Cell Biology", 
        "type": "DefinedTerm"
      }, 
      {
        "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/06", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Biological Sciences", 
        "type": "DefinedTerm"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "Universit\u00e9 des Sciences et de la Technologie d'Oran Mohamed Boudiaf", 
          "id": "https://www.grid.ac/institutes/grid.442511.7", 
          "name": [
            "Department of Chemistry, Faculty of Sciences, Taibah University, PO Box 344, Al-Madinah Al-Munawarah, Saudi Arabia", 
            "Laboratoire de Chimie and Electrochimie des Complexes M\u00e9talliques (LCECM), Department of Chemistry, Faculty of Sciences, University of Sciences and Technology Mohamed Boudiaf, USTO-MB, PO Box 1505, Oran, El M\u2019nouar, Algeria"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Rezki", 
        "givenName": "Nadjet", 
        "id": "sg:person.0604030744.39", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0604030744.39"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Taibah University", 
          "id": "https://www.grid.ac/institutes/grid.412892.4", 
          "name": [
            "Department of Chemistry, Faculty of Sciences, Taibah University, PO Box 344, Al-Madinah Al-Munawarah, Saudi Arabia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Mayaba", 
        "givenName": "Mariem Mohammed", 
        "id": "sg:person.015032703145.36", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015032703145.36"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Taibah University", 
          "id": "https://www.grid.ac/institutes/grid.412892.4", 
          "name": [
            "Department of Chemistry, Faculty of Sciences, Taibah University, PO Box 344, Al-Madinah Al-Munawarah, Saudi Arabia"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Al-blewi", 
        "givenName": "Fawzia Faleh", 
        "id": "sg:person.016425644145.50", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016425644145.50"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Universit\u00e9 des Sciences et de la Technologie d'Oran Mohamed Boudiaf", 
          "id": "https://www.grid.ac/institutes/grid.442511.7", 
          "name": [
            "Department of Chemistry, Faculty of Sciences, Taibah University, PO Box 344, Al-Madinah Al-Munawarah, Saudi Arabia", 
            "Laboratoire de Chimie and Electrochimie des Complexes M\u00e9talliques (LCECM), Department of Chemistry, Faculty of Sciences, University of Sciences and Technology Mohamed Boudiaf, USTO-MB, PO Box 1505, Oran, El M\u2019nouar, Algeria"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Aouad", 
        "givenName": "Mohamed Reda", 
        "id": "sg:person.01242641720.33", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01242641720.33"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Alexandria University", 
          "id": "https://www.grid.ac/institutes/grid.7155.6", 
          "name": [
            "Chemistry Department, Faculty of Science, Alexandria University, Alexandria, Egypt"
          ], 
          "type": "Organization"
        }, 
        "familyName": "El Ashry", 
        "givenName": "El Sayed Helmi", 
        "id": "sg:person.013346776112.31", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013346776112.31"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "https://doi.org/10.1002/jhet.5570450511", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1000497960"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/jhet.5570450511", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1000497960"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1080/14756360701425014", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1002331145"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.colsurfa.2011.12.014", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1002456417"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/cr0783479", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1003689578"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/cr0783479", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1003689578"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.jcis.2011.07.049", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1005467285"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1046/j.1469-0691.2000.00142.x", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1007617940"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.carres.2009.01.026", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1009112411"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/ps.2780170414", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1009401225"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.tetlet.2012.01.102", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1013509763"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.colsurfa.2012.11.004", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1014726072"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.jfluchem.2006.06.007", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1021551030"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/ardp.201500292", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1025334225"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.carres.2011.11.020", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1026441077"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1002/1521-3773(20020715)41:14<2596::aid-anie2596>3.0.co;2-4", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1028820752"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.3390/molecules20058666", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1031356264"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.3390/molecules20058666", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1031356264"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.bioorg.2015.11.005", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1034086618"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.bmc.2015.10.042", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1044473096"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.bmc.2008.08.008", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1045192950"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1016/j.molstruc.2008.05.028", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1047638429"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1080/15257770.2015.1109098", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1049992837"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1080/15257770.2012.751491", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1052746739"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm00298a021", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055941889"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm990373e", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055959575"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.1021/jm990373e", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1055959575"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.2174/156802606777951073", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1069193386"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.2174/157018013804142429", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1069202452"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://doi.org/10.2174/1871520615666150819121106", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1069219184"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "https://app.dimensions.ai/details/publication/pub.1083245742", 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2017-02", 
    "datePublishedReg": "2017-02-01", 
    "description": "Base-catalyzed alkylation of 5-(4-fluorophenyl)-2,4-dihydro-1,2,4-triazole-3-thione (3) with one or two equivalents of propargyl bromide in presence of triethylamine as catalyst selectively produced the thiopropargylated 1,2,4-triazole 7 in 90 % yield. Under the same reaction conditions, 4-ethyl-5-(4-fluorophenyl)-3-(prop-2-yn-1-ylthio)-1,2,4-triazole (8) was produced. Conversely, when the propargylation was carried out in presence of sodium bicarbonate, a mixture of S,N4- (24) and S,N2-bis(propargylated) triazoles (25) was obtained in 85 % overall yield. The click 1,3-dipolar cycloaddition reaction of the mono- (7, 8) and/or bis(propargylated)-1,2,4-triazoles (24) with a variety of long-chain alkyl azides, conducted in t-BuOH:H2O (10:1) in presence of sodium ascorbate and copper(II) sulfate at room temperature, afforded the regioselective 1,4-disubstituted mono- (14\u201318) and bis(1,2,3-triazole) derivatives (26\u201330) containing a fluorinated 1,2,4-triazole moiety and a lipophilic side chain. The structures of the new products were elucidated by infrared (IR), 1H and 13C nuclear magnetic resonance (NMR), and mass spectrometry. They were also assessed in vitro for their antimicrobial potency against six bacteria (Bacillus subtilis, Streptococcus pneumonia, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumonia) and two fungi (Aspergillus fumigatus and Candida albicans). The bioassay results revealed that some of the tested compounds displayed promising antimicrobial activity.", 
    "genre": "research_article", 
    "id": "sg:pub.10.1007/s11164-016-2679-4", 
    "inLanguage": [
      "en"
    ], 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1127880", 
        "issn": [
          "0922-6168", 
          "1568-5675"
        ], 
        "name": "Research on Chemical Intermediates", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "2", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "43"
      }
    ], 
    "name": "Click 1,4-regioselective synthesis, characterization, and antimicrobial screening of novel 1,2,3-triazoles tethering fluorinated 1,2,4-triazole and lipophilic side chain", 
    "pagination": "995-1011", 
    "productId": [
      {
        "name": "readcube_id", 
        "type": "PropertyValue", 
        "value": [
          "d06c9bd417d77b1928810c8b50740ff6eae968f06a3f44a813ebfe9e8fdb71c3"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s11164-016-2679-4"
        ]
      }, 
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1043755371"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s11164-016-2679-4", 
      "https://app.dimensions.ai/details/publication/pub.1043755371"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2019-04-11T12:42", 
    "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/v90/0000000363_0000000363/records_70061_00000001.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://link.springer.com/10.1007%2Fs11164-016-2679-4"
  }
]
 

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/s11164-016-2679-4'

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/s11164-016-2679-4'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s11164-016-2679-4'

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

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s11164-016-2679-4'


 

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

176 TRIPLES      21 PREDICATES      54 URIs      19 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s11164-016-2679-4 schema:about anzsrc-for:06
2 anzsrc-for:0601
3 schema:author N59d782f60884475fbfb392f330f6674b
4 schema:citation https://app.dimensions.ai/details/publication/pub.1083245742
5 https://doi.org/10.1002/1521-3773(20020715)41:14<2596::aid-anie2596>3.0.co;2-4
6 https://doi.org/10.1002/ardp.201500292
7 https://doi.org/10.1002/jhet.5570450511
8 https://doi.org/10.1002/ps.2780170414
9 https://doi.org/10.1016/j.bioorg.2015.11.005
10 https://doi.org/10.1016/j.bmc.2008.08.008
11 https://doi.org/10.1016/j.bmc.2015.10.042
12 https://doi.org/10.1016/j.carres.2009.01.026
13 https://doi.org/10.1016/j.carres.2011.11.020
14 https://doi.org/10.1016/j.colsurfa.2011.12.014
15 https://doi.org/10.1016/j.colsurfa.2012.11.004
16 https://doi.org/10.1016/j.jcis.2011.07.049
17 https://doi.org/10.1016/j.jfluchem.2006.06.007
18 https://doi.org/10.1016/j.molstruc.2008.05.028
19 https://doi.org/10.1016/j.tetlet.2012.01.102
20 https://doi.org/10.1021/cr0783479
21 https://doi.org/10.1021/jm00298a021
22 https://doi.org/10.1021/jm990373e
23 https://doi.org/10.1046/j.1469-0691.2000.00142.x
24 https://doi.org/10.1080/14756360701425014
25 https://doi.org/10.1080/15257770.2012.751491
26 https://doi.org/10.1080/15257770.2015.1109098
27 https://doi.org/10.2174/156802606777951073
28 https://doi.org/10.2174/157018013804142429
29 https://doi.org/10.2174/1871520615666150819121106
30 https://doi.org/10.3390/molecules20058666
31 schema:datePublished 2017-02
32 schema:datePublishedReg 2017-02-01
33 schema:description Base-catalyzed alkylation of 5-(4-fluorophenyl)-2,4-dihydro-1,2,4-triazole-3-thione (3) with one or two equivalents of propargyl bromide in presence of triethylamine as catalyst selectively produced the thiopropargylated 1,2,4-triazole 7 in 90 % yield. Under the same reaction conditions, 4-ethyl-5-(4-fluorophenyl)-3-(prop-2-yn-1-ylthio)-1,2,4-triazole (8) was produced. Conversely, when the propargylation was carried out in presence of sodium bicarbonate, a mixture of S,N4- (24) and S,N2-bis(propargylated) triazoles (25) was obtained in 85 % overall yield. The click 1,3-dipolar cycloaddition reaction of the mono- (7, 8) and/or bis(propargylated)-1,2,4-triazoles (24) with a variety of long-chain alkyl azides, conducted in t-BuOH:H2O (10:1) in presence of sodium ascorbate and copper(II) sulfate at room temperature, afforded the regioselective 1,4-disubstituted mono- (14–18) and bis(1,2,3-triazole) derivatives (26–30) containing a fluorinated 1,2,4-triazole moiety and a lipophilic side chain. The structures of the new products were elucidated by infrared (IR), 1H and 13C nuclear magnetic resonance (NMR), and mass spectrometry. They were also assessed in vitro for their antimicrobial potency against six bacteria (Bacillus subtilis, Streptococcus pneumonia, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumonia) and two fungi (Aspergillus fumigatus and Candida albicans). The bioassay results revealed that some of the tested compounds displayed promising antimicrobial activity.
34 schema:genre research_article
35 schema:inLanguage en
36 schema:isAccessibleForFree false
37 schema:isPartOf Nc7ff85fac1c048969b0e315e9afb2585
38 Ndc14b4280a844316a2fabd0ce61a10cc
39 sg:journal.1127880
40 schema:name Click 1,4-regioselective synthesis, characterization, and antimicrobial screening of novel 1,2,3-triazoles tethering fluorinated 1,2,4-triazole and lipophilic side chain
41 schema:pagination 995-1011
42 schema:productId N001ce771995a41ff9a6a26cdd36090ad
43 N0164f8a13dc04e73afda9b2835b47cca
44 Na9e23520b080476caa7624bd85bc208f
45 schema:sameAs https://app.dimensions.ai/details/publication/pub.1043755371
46 https://doi.org/10.1007/s11164-016-2679-4
47 schema:sdDatePublished 2019-04-11T12:42
48 schema:sdLicense https://scigraph.springernature.com/explorer/license/
49 schema:sdPublisher N8197bc8e8f594cd5adc414ca92c82592
50 schema:url https://link.springer.com/10.1007%2Fs11164-016-2679-4
51 sgo:license sg:explorer/license/
52 sgo:sdDataset articles
53 rdf:type schema:ScholarlyArticle
54 N001ce771995a41ff9a6a26cdd36090ad schema:name dimensions_id
55 schema:value pub.1043755371
56 rdf:type schema:PropertyValue
57 N0164f8a13dc04e73afda9b2835b47cca schema:name readcube_id
58 schema:value d06c9bd417d77b1928810c8b50740ff6eae968f06a3f44a813ebfe9e8fdb71c3
59 rdf:type schema:PropertyValue
60 N01bdfa0b4c27400b9ff8ac77a32d3881 rdf:first sg:person.013346776112.31
61 rdf:rest rdf:nil
62 N05adae6676b3488097bfc1791cb1a4db rdf:first sg:person.01242641720.33
63 rdf:rest N01bdfa0b4c27400b9ff8ac77a32d3881
64 N419992948c334d89868c5dc4bd7ec5f6 rdf:first sg:person.015032703145.36
65 rdf:rest Nbebb7e973e23492789c4840985d1bb07
66 N59d782f60884475fbfb392f330f6674b rdf:first sg:person.0604030744.39
67 rdf:rest N419992948c334d89868c5dc4bd7ec5f6
68 N8197bc8e8f594cd5adc414ca92c82592 schema:name Springer Nature - SN SciGraph project
69 rdf:type schema:Organization
70 Na9e23520b080476caa7624bd85bc208f schema:name doi
71 schema:value 10.1007/s11164-016-2679-4
72 rdf:type schema:PropertyValue
73 Nbebb7e973e23492789c4840985d1bb07 rdf:first sg:person.016425644145.50
74 rdf:rest N05adae6676b3488097bfc1791cb1a4db
75 Nc7ff85fac1c048969b0e315e9afb2585 schema:issueNumber 2
76 rdf:type schema:PublicationIssue
77 Ndc14b4280a844316a2fabd0ce61a10cc schema:volumeNumber 43
78 rdf:type schema:PublicationVolume
79 anzsrc-for:06 schema:inDefinedTermSet anzsrc-for:
80 schema:name Biological Sciences
81 rdf:type schema:DefinedTerm
82 anzsrc-for:0601 schema:inDefinedTermSet anzsrc-for:
83 schema:name Biochemistry and Cell Biology
84 rdf:type schema:DefinedTerm
85 sg:journal.1127880 schema:issn 0922-6168
86 1568-5675
87 schema:name Research on Chemical Intermediates
88 rdf:type schema:Periodical
89 sg:person.01242641720.33 schema:affiliation https://www.grid.ac/institutes/grid.442511.7
90 schema:familyName Aouad
91 schema:givenName Mohamed Reda
92 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01242641720.33
93 rdf:type schema:Person
94 sg:person.013346776112.31 schema:affiliation https://www.grid.ac/institutes/grid.7155.6
95 schema:familyName El Ashry
96 schema:givenName El Sayed Helmi
97 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.013346776112.31
98 rdf:type schema:Person
99 sg:person.015032703145.36 schema:affiliation https://www.grid.ac/institutes/grid.412892.4
100 schema:familyName Mayaba
101 schema:givenName Mariem Mohammed
102 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015032703145.36
103 rdf:type schema:Person
104 sg:person.016425644145.50 schema:affiliation https://www.grid.ac/institutes/grid.412892.4
105 schema:familyName Al-blewi
106 schema:givenName Fawzia Faleh
107 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.016425644145.50
108 rdf:type schema:Person
109 sg:person.0604030744.39 schema:affiliation https://www.grid.ac/institutes/grid.442511.7
110 schema:familyName Rezki
111 schema:givenName Nadjet
112 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0604030744.39
113 rdf:type schema:Person
114 https://app.dimensions.ai/details/publication/pub.1083245742 schema:CreativeWork
115 https://doi.org/10.1002/1521-3773(20020715)41:14<2596::aid-anie2596>3.0.co;2-4 schema:sameAs https://app.dimensions.ai/details/publication/pub.1028820752
116 rdf:type schema:CreativeWork
117 https://doi.org/10.1002/ardp.201500292 schema:sameAs https://app.dimensions.ai/details/publication/pub.1025334225
118 rdf:type schema:CreativeWork
119 https://doi.org/10.1002/jhet.5570450511 schema:sameAs https://app.dimensions.ai/details/publication/pub.1000497960
120 rdf:type schema:CreativeWork
121 https://doi.org/10.1002/ps.2780170414 schema:sameAs https://app.dimensions.ai/details/publication/pub.1009401225
122 rdf:type schema:CreativeWork
123 https://doi.org/10.1016/j.bioorg.2015.11.005 schema:sameAs https://app.dimensions.ai/details/publication/pub.1034086618
124 rdf:type schema:CreativeWork
125 https://doi.org/10.1016/j.bmc.2008.08.008 schema:sameAs https://app.dimensions.ai/details/publication/pub.1045192950
126 rdf:type schema:CreativeWork
127 https://doi.org/10.1016/j.bmc.2015.10.042 schema:sameAs https://app.dimensions.ai/details/publication/pub.1044473096
128 rdf:type schema:CreativeWork
129 https://doi.org/10.1016/j.carres.2009.01.026 schema:sameAs https://app.dimensions.ai/details/publication/pub.1009112411
130 rdf:type schema:CreativeWork
131 https://doi.org/10.1016/j.carres.2011.11.020 schema:sameAs https://app.dimensions.ai/details/publication/pub.1026441077
132 rdf:type schema:CreativeWork
133 https://doi.org/10.1016/j.colsurfa.2011.12.014 schema:sameAs https://app.dimensions.ai/details/publication/pub.1002456417
134 rdf:type schema:CreativeWork
135 https://doi.org/10.1016/j.colsurfa.2012.11.004 schema:sameAs https://app.dimensions.ai/details/publication/pub.1014726072
136 rdf:type schema:CreativeWork
137 https://doi.org/10.1016/j.jcis.2011.07.049 schema:sameAs https://app.dimensions.ai/details/publication/pub.1005467285
138 rdf:type schema:CreativeWork
139 https://doi.org/10.1016/j.jfluchem.2006.06.007 schema:sameAs https://app.dimensions.ai/details/publication/pub.1021551030
140 rdf:type schema:CreativeWork
141 https://doi.org/10.1016/j.molstruc.2008.05.028 schema:sameAs https://app.dimensions.ai/details/publication/pub.1047638429
142 rdf:type schema:CreativeWork
143 https://doi.org/10.1016/j.tetlet.2012.01.102 schema:sameAs https://app.dimensions.ai/details/publication/pub.1013509763
144 rdf:type schema:CreativeWork
145 https://doi.org/10.1021/cr0783479 schema:sameAs https://app.dimensions.ai/details/publication/pub.1003689578
146 rdf:type schema:CreativeWork
147 https://doi.org/10.1021/jm00298a021 schema:sameAs https://app.dimensions.ai/details/publication/pub.1055941889
148 rdf:type schema:CreativeWork
149 https://doi.org/10.1021/jm990373e schema:sameAs https://app.dimensions.ai/details/publication/pub.1055959575
150 rdf:type schema:CreativeWork
151 https://doi.org/10.1046/j.1469-0691.2000.00142.x schema:sameAs https://app.dimensions.ai/details/publication/pub.1007617940
152 rdf:type schema:CreativeWork
153 https://doi.org/10.1080/14756360701425014 schema:sameAs https://app.dimensions.ai/details/publication/pub.1002331145
154 rdf:type schema:CreativeWork
155 https://doi.org/10.1080/15257770.2012.751491 schema:sameAs https://app.dimensions.ai/details/publication/pub.1052746739
156 rdf:type schema:CreativeWork
157 https://doi.org/10.1080/15257770.2015.1109098 schema:sameAs https://app.dimensions.ai/details/publication/pub.1049992837
158 rdf:type schema:CreativeWork
159 https://doi.org/10.2174/156802606777951073 schema:sameAs https://app.dimensions.ai/details/publication/pub.1069193386
160 rdf:type schema:CreativeWork
161 https://doi.org/10.2174/157018013804142429 schema:sameAs https://app.dimensions.ai/details/publication/pub.1069202452
162 rdf:type schema:CreativeWork
163 https://doi.org/10.2174/1871520615666150819121106 schema:sameAs https://app.dimensions.ai/details/publication/pub.1069219184
164 rdf:type schema:CreativeWork
165 https://doi.org/10.3390/molecules20058666 schema:sameAs https://app.dimensions.ai/details/publication/pub.1031356264
166 rdf:type schema:CreativeWork
167 https://www.grid.ac/institutes/grid.412892.4 schema:alternateName Taibah University
168 schema:name Department of Chemistry, Faculty of Sciences, Taibah University, PO Box 344, Al-Madinah Al-Munawarah, Saudi Arabia
169 rdf:type schema:Organization
170 https://www.grid.ac/institutes/grid.442511.7 schema:alternateName Université des Sciences et de la Technologie d'Oran Mohamed Boudiaf
171 schema:name Department of Chemistry, Faculty of Sciences, Taibah University, PO Box 344, Al-Madinah Al-Munawarah, Saudi Arabia
172 Laboratoire de Chimie and Electrochimie des Complexes Métalliques (LCECM), Department of Chemistry, Faculty of Sciences, University of Sciences and Technology Mohamed Boudiaf, USTO-MB, PO Box 1505, Oran, El M’nouar, Algeria
173 rdf:type schema:Organization
174 https://www.grid.ac/institutes/grid.7155.6 schema:alternateName Alexandria University
175 schema:name Chemistry Department, Faculty of Science, Alexandria University, Alexandria, Egypt
176 rdf:type schema:Organization
 




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


...