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Synthesis of (E)-(4-(Aryl)phenyl)(3-(2-(1-phenyl-3-(thiophen-2-yl)-1H-pyrazol-4-yl)vinyl)benzofuran-2-yl)methanones by Claisen Schmidt-Suzuki Cross Coupling and their Antibacterial and Antifungal Activity
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Synthesis of (E)-(4-(Aryl)phenyl)(3-(2-(1-phenyl-3-(thiophen-2-yl)-1H-pyrazol-4-yl)vinyl)benzofuran-2-yl)methanones by Claisen Schmidt-Suzuki Cross Coupling and their Antibacterial and Antifungal Activity

Journal of the Mexican Chemical Society, 2017-09, Vol.61 (3), p.167-176 [Peer Reviewed Journal]

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. ;ISSN: 1870-249X ;DOI: 10.29356/jmcs.v61i3.342

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2
Reações de acoplamento cruzado de organossilanos catalisadas por paládio: aspectos históricos, sintéticos e mecanísticos
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Reações de acoplamento cruzado de organossilanos catalisadas por paládio: aspectos históricos, sintéticos e mecanísticos

Química Nova, 2007, Vol.30 (7), p.1704-1720 [Peer Reviewed Journal]

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. ;ISSN: 0100-4042 ;ISSN: 1678-7064 ;DOI: 10.1590/S0100-40422007000700038

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3
Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds
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Recent Progress in the Use of Pd-Catalyzed C-C Cross-Coupling Reactions in the Synthesis of Pharmaceutical Compounds

Journal of the Brazilian Chemical Society, 2014-12, Vol.25 (12), p.2186-2214 [Peer Reviewed Journal]

This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 International License. ;ISSN: 0103-5053 ;ISSN: 1678-4790 ;EISSN: 1678-4790 ;DOI: 10.5935/0103-5053.20140255

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4
Pd-catalyzed Suzuki cross-Coupling reaction of bromostilbene: insights on the nature of the boron Species
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Pd-catalyzed Suzuki cross-Coupling reaction of bromostilbene: insights on the nature of the boron Species

Journal of the Brazilian Chemical Society, 2007, Vol.18 (7), p.1443-1447 [Peer Reviewed Journal]

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. ;ISSN: 0103-5053 ;ISSN: 1678-4790 ;EISSN: 1678-4790 ;DOI: 10.1590/S0103-50532007000700021

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