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1
Palladium-Catalyzed Desulfitative Cross-Coupling Reaction of Sodium Arylsulfinates with H-Phosphonate Diesters
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Palladium-Catalyzed Desulfitative Cross-Coupling Reaction of Sodium Arylsulfinates with H-Phosphonate Diesters

Advanced synthesis & catalysis, 2014-03, Vol.356 (5), p.967-971 [Peer Reviewed Journal]

2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1615-4150 ;EISSN: 1615-4169 ;DOI: 10.1002/adsc.201300983

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2
High-Turnover Palladium Catalysts in Cross-Coupling and Heck Chemistry: A Critical Overview
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High-Turnover Palladium Catalysts in Cross-Coupling and Heck Chemistry: A Critical Overview

Advanced synthesis & catalysis, 2004-12, Vol.346 (13-15), p.1553-1582 [Peer Reviewed Journal]

Copyright © 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1615-4150 ;EISSN: 1615-4169 ;DOI: 10.1002/adsc.200404178

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3
A Polymer-Bound Monodentate-P-Ligated Palladium Complex as a Recyclable Catalyst for the Suzuki-Miyaura Coupling Reaction of Aryl Chlorides
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A Polymer-Bound Monodentate-P-Ligated Palladium Complex as a Recyclable Catalyst for the Suzuki-Miyaura Coupling Reaction of Aryl Chlorides

Advanced synthesis & catalysis, 2015-08, Vol.357 (11), p.2503-2508 [Peer Reviewed Journal]

2015 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1615-4150 ;EISSN: 1615-4169 ;DOI: 10.1002/adsc.201500070

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4
Immobilized Pd on (S)-methyl histidinate-modified multi-walled carbon nanotubes: a powerful and recyclable catalyst for Mizoroki-Heck and Suzuki-Miyaura C-C cross-coupling reactions in green solvents and under mild conditions
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Immobilized Pd on (S)-methyl histidinate-modified multi-walled carbon nanotubes: a powerful and recyclable catalyst for Mizoroki-Heck and Suzuki-Miyaura C-C cross-coupling reactions in green solvents and under mild conditions

Applied organometallic chemistry, 2016-05, Vol.30 (5), p.256-261 [Peer Reviewed Journal]

Copyright © 2016 John Wiley & Sons, Ltd. ;ISSN: 0268-2605 ;EISSN: 1099-0739 ;DOI: 10.1002/aoc.3425

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5
Preparation, Characterization, and Catalytic Properties of Pd-Graphene Quantum Dot Catalysts
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Preparation, Characterization, and Catalytic Properties of Pd-Graphene Quantum Dot Catalysts

Catalysts, 2022-06, Vol.12 (6), p.619 [Peer Reviewed Journal]

2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2073-4344 ;EISSN: 2073-4344 ;DOI: 10.3390/catal12060619

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6
Single-atom Pd catalyst anchored on Zr-based metal-organic polyhedra for Suzuki-Miyaura cross coupling reactions in aqueous media
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Single-atom Pd catalyst anchored on Zr-based metal-organic polyhedra for Suzuki-Miyaura cross coupling reactions in aqueous media

Nano research, 2021-02, Vol.14 (2), p.486-492 [Peer Reviewed Journal]

Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature 2020 ;Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature 2020. ;ISSN: 1998-0124 ;EISSN: 1998-0000 ;DOI: 10.1007/s12274-020-2885-7

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7
Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond
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Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond

Catalysts, 2020-01, Vol.10 (1), p.4 [Peer Reviewed Journal]

2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2073-4344 ;EISSN: 2073-4344 ;DOI: 10.3390/catal10010004

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8
Recent Advances in the Applications of the Intramolecular Suzuki Cross-coupling Reaction in Cyclization and Heterocyclization: An Update
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Recent Advances in the Applications of the Intramolecular Suzuki Cross-coupling Reaction in Cyclization and Heterocyclization: An Update

Current organic chemistry, 2019-01, Vol.23 (22), p.2469-2488 [Peer Reviewed Journal]

ISSN: 1385-2728 ;EISSN: 1875-5348 ;DOI: 10.2174/1385272823666191023115842

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9
Iminophosphine palladium(II) complexes: synthesis, characterization, and application in Heck cross-coupling reaction of aryl bromides
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Iminophosphine palladium(II) complexes: synthesis, characterization, and application in Heck cross-coupling reaction of aryl bromides

Applied organometallic chemistry, 2014-07, Vol.28 (7), p.529-536 [Peer Reviewed Journal]

Copyright © 2014 John Wiley & Sons, Ltd. ;ISSN: 0268-2605 ;EISSN: 1099-0739 ;DOI: 10.1002/aoc.3158

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10
Fabrication of covalently functionalized mesoporous silica core-shell magnetite nanoparticles with palladium(II) acetylacetonate: application as a magnetically separable nanocatalyst for Suzuki cross-coupling reaction of acyl halides with boronic acids
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Fabrication of covalently functionalized mesoporous silica core-shell magnetite nanoparticles with palladium(II) acetylacetonate: application as a magnetically separable nanocatalyst for Suzuki cross-coupling reaction of acyl halides with boronic acids

Applied organometallic chemistry, 2015-04, Vol.29 (4), p.247-253 [Peer Reviewed Journal]

Copyright © 2015 John Wiley & Sons, Ltd. ;ISSN: 0268-2605 ;EISSN: 1099-0739 ;DOI: 10.1002/aoc.3280

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11
Preparation of Synthetic and Natural Derivatives of Flavonoids Using Suzuki-Miyaura Cross-Coupling Reaction
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Preparation of Synthetic and Natural Derivatives of Flavonoids Using Suzuki-Miyaura Cross-Coupling Reaction

Molecules (Basel, Switzerland), 2022-01, Vol.27 (3), p.967 [Peer Reviewed Journal]

2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2022 by the authors. 2022 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules27030967 ;PMID: 35164232

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12
Highly Active Fe3O4@SBA-15@NHC-Pd Catalyst for Suzuki–Miyaura Cross-Coupling Reaction
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Highly Active Fe3O4@SBA-15@NHC-Pd Catalyst for Suzuki–Miyaura Cross-Coupling Reaction

Catalysis letters, 2022-06, Vol.152 (6), p.1621-1638 [Peer Reviewed Journal]

The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021 ;The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021. ;ISSN: 1011-372X ;EISSN: 1572-879X ;DOI: 10.1007/s10562-021-03755-w

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13
Palladium Mesoionic Carbene Pre-catalyst for General Cross-Coupling Transformations in Deep Eutectic Solvents
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Palladium Mesoionic Carbene Pre-catalyst for General Cross-Coupling Transformations in Deep Eutectic Solvents

Frontiers in chemistry, 2019-10, Vol.7, p.700-700 [Peer Reviewed Journal]

Copyright © 2019 Marset, Saavedra, González-Gallardo, Beaton, León, Luna, Ramón and Guillena. 2019 Marset, Saavedra, González-Gallardo, Beaton, León, Luna, Ramón and Guillena ;ISSN: 2296-2646 ;EISSN: 2296-2646 ;DOI: 10.3389/fchem.2019.00700 ;PMID: 31709230

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14
A sustainable strategy for production and functionalization of nanocelluloses
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Article
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A sustainable strategy for production and functionalization of nanocelluloses

Pure and applied chemistry, 2019-05, Vol.91 (5), p.865 [Peer Reviewed Journal]

ISSN: 0033-4545 ;ISSN: 1365-3075 ;EISSN: 1365-3075 ;DOI: 10.1515/pac-2018-0204

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15
An alternative C–P cross-coupling route for the synthesis of novel V-shaped aryldiphosphonic acids
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An alternative C–P cross-coupling route for the synthesis of novel V-shaped aryldiphosphonic acids

Beilstein journal of organic chemistry, 2022-11, Vol.18, p.1518-1523 [Peer Reviewed Journal]

Copyright Beilstein-Institut zur Föerderung der Chemischen Wissenschaften 2022 ;Copyright © 2022, Shearan et al. 2022 Shearan et al. ;ISSN: 1860-5397 ;ISSN: 2195-951X ;EISSN: 1860-5397 ;DOI: 10.3762/bjoc.18.160

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16
Synthesis, characterization and catalytic activity of new aminomethyldiphosphine-Pd(II) complexes for Suzuki cross-coupling reaction
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Synthesis, characterization and catalytic activity of new aminomethyldiphosphine-Pd(II) complexes for Suzuki cross-coupling reaction

Applied organometallic chemistry, 2014-02, Vol.28 (2), p.91-94 [Peer Reviewed Journal]

Copyright © 2013 John Wiley & Sons, Ltd. ;ISSN: 0268-2605 ;EISSN: 1099-0739 ;DOI: 10.1002/aoc.3085

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17
Magnetic Nanoparticle-Supported N-Heterocyclic Carbene-Palladium(II): A Convenient, Efficient and Recyclable Catalyst for Suzuki–Miyaura Cross-Coupling Reactions
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Magnetic Nanoparticle-Supported N-Heterocyclic Carbene-Palladium(II): A Convenient, Efficient and Recyclable Catalyst for Suzuki–Miyaura Cross-Coupling Reactions

Catalysis letters, 2017-04, Vol.147 (4), p.900-918 [Peer Reviewed Journal]

Springer Science+Business Media New York 2017 ;COPYRIGHT 2017 Springer ;Catalysis Letters is a copyright of Springer, (2017). All Rights Reserved. ;ISSN: 1011-372X ;EISSN: 1572-879X ;DOI: 10.1007/s10562-017-1987-7

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18
Hiyama cross-coupling reaction catalyzed by a palladium salt of 1-benzyl-4-aza-1-azoniabicyclo[2.2.2]octane chloride under microwave irradiation
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Article
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Hiyama cross-coupling reaction catalyzed by a palladium salt of 1-benzyl-4-aza-1-azoniabicyclo[2.2.2]octane chloride under microwave irradiation

Applied organometallic chemistry, 2014-04, Vol.28 (4), p.217-220 [Peer Reviewed Journal]

Copyright © 2014 John Wiley & Sons, Ltd. ;ISSN: 0268-2605 ;EISSN: 1099-0739 ;DOI: 10.1002/aoc.3100

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19
Mild and Ligand-Free Palladium-Catalyzed Cross-Couplings between Aryl Halides and Arylboronic Acids for the Synthesis of Biaryls and Heterocycle-Containing Biaryls
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Mild and Ligand-Free Palladium-Catalyzed Cross-Couplings between Aryl Halides and Arylboronic Acids for the Synthesis of Biaryls and Heterocycle-Containing Biaryls

European Journal of Organic Chemistry, 2007-03, Vol.2007 (9), p.1457-1462 [Peer Reviewed Journal]

Copyright © 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1434-193X ;EISSN: 1099-0690 ;DOI: 10.1002/ejoc.200600879

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20
Cross coupling reactions catalyzed by (NHC)Pd(II) complexes
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Cross coupling reactions catalyzed by (NHC)Pd(II) complexes

Turkish journal of chemistry, 2015, Vol.39, p.1115-1157 [Peer Reviewed Journal]

ISSN: 1300-0527 ;EISSN: 1303-6130 ;DOI: 10.3906/kim-1510-31

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