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1
Recent advances in noble metal nanocatalysts for Suzuki and Heck cross-coupling reactions
Recent advances in noble metal nanocatalysts for Suzuki and Heck cross-coupling reactions
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Recent advances in noble metal nanocatalysts for Suzuki and Heck cross-coupling reactions

Molecules, 2010-03, Vol.15 (4), p.2124-2138 [Peer Reviewed Journal]

Copyright MDPI AG 2010 ;2010 by the authors; 2010 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules15042124 ;PMID: 20428032

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2
Biogenic palladium nanostructures for Suzuki-Miyaura and Sonogashira cross-coupling reaction under mild reaction conditions
Biogenic palladium nanostructures for Suzuki-Miyaura and Sonogashira cross-coupling reaction under mild reaction conditions
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Biogenic palladium nanostructures for Suzuki-Miyaura and Sonogashira cross-coupling reaction under mild reaction conditions

Current research in green and sustainable chemistry, 2022, Vol.5, p.100301, Article 100301 [Peer Reviewed Journal]

2022 The Authors ;ISSN: 2666-0865 ;EISSN: 2666-0865 ;DOI: 10.1016/j.crgsc.2022.100301

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3
Investigating the Effects of Fluorine Substituents on Organic Dyes in Dye-Sensitized Solar Cells
Investigating the Effects of Fluorine Substituents on Organic Dyes in Dye-Sensitized Solar Cells
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Investigating the Effects of Fluorine Substituents on Organic Dyes in Dye-Sensitized Solar Cells

Journal of the Turkish Chemical Society, Section A, Chemistry, 2024-02, Vol.11 (1), p.1-10 [Peer Reviewed Journal]

ISSN: 2149-0120 ;EISSN: 2149-0120 ;DOI: 10.18596/jotcsa.1355244

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4
N-Methylphthalimide-substituted benzimidazolium salts and PEPPSI Pd-NHC complexes: synthesis, characterization and catalytic activity in carbon-carbon bond-forming reactions
N-Methylphthalimide-substituted benzimidazolium salts and PEPPSI Pd-NHC complexes: synthesis, characterization and catalytic activity in carbon-carbon bond-forming reactions
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N-Methylphthalimide-substituted benzimidazolium salts and PEPPSI Pd-NHC complexes: synthesis, characterization and catalytic activity in carbon-carbon bond-forming reactions

Beilstein journal of organic chemistry, 2016-01, Vol.12 (1), p.81-88 [Peer Reviewed Journal]

Copyright © 2016, Akkoç et al; licensee Beilstein-Institut. This work is licensed under the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright © 2016, Akkoç et al. 2016 Akkoç et al. ;ISSN: 1860-5397 ;ISSN: 2195-951X ;EISSN: 1860-5397 ;DOI: 10.3762/bjoc.12.9 ;PMID: 26877810

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5
Pd Nanocatalyst Adorned on Magnetic Chitosan@N-Heterocyclic Carbene: Eco-Compatible Suzuki Cross-Coupling Reaction
Pd Nanocatalyst Adorned on Magnetic Chitosan@N-Heterocyclic Carbene: Eco-Compatible Suzuki Cross-Coupling Reaction
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Pd Nanocatalyst Adorned on Magnetic Chitosan@N-Heterocyclic Carbene: Eco-Compatible Suzuki Cross-Coupling Reaction

Molecules (Basel, Switzerland), 2019-08, Vol.24 (17), p.3048 [Peer Reviewed Journal]

2019 by the authors. 2019 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules24173048 ;PMID: 31443412

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6
Preparation, Characterization, and Catalytic Properties of Pd-Graphene Quantum Dot Catalysts
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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7
Palladacyclic N-heterocyclic carbene precatalysts for transition metal catalysis
Palladacyclic N-heterocyclic carbene precatalysts for transition metal catalysis
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Palladacyclic N-heterocyclic carbene precatalysts for transition metal catalysis

Green synthesis and catalysis, 2022-11, Vol.3 (4), p.327-338 [Peer Reviewed Journal]

ISSN: 2666-5549 ;EISSN: 2666-5549 ;DOI: 10.1016/j.gresc.2022.06.008

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8
Effective Synthesis of a Novel Betulinic Acid Conjugate with Mitochondria-Targeting Cation F16
Effective Synthesis of a Novel Betulinic Acid Conjugate with Mitochondria-Targeting Cation F16
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Conference Proceeding 		Add to My Research

Effective Synthesis of a Novel Betulinic Acid Conjugate with Mitochondria-Targeting Cation F16

Chemistry Proceedings, 2021, Vol.8 (1), p.97 [Peer Reviewed Journal]

EISSN: 2673-4583 ;DOI: 10.3390/ecsoc-25-11638

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9
Recent Advances in Catalytic Alkyne Transformation via Copper Carbene Intermediates
Recent Advances in Catalytic Alkyne Transformation via Copper Carbene Intermediates
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Recent Advances in Catalytic Alkyne Transformation via Copper Carbene Intermediates

Molecules (Basel, Switzerland), 2022-05, Vol.27 (10), p.3088 [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/molecules27103088 ;PMID: 35630567

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10
Rational Design of Bifunctional Microporous Organic Polymers Containing Anthracene and Triphenylamine Units for Energy Storage and Biological Applications
Rational Design of Bifunctional Microporous Organic Polymers Containing Anthracene and Triphenylamine Units for Energy Storage and Biological Applications
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Rational Design of Bifunctional Microporous Organic Polymers Containing Anthracene and Triphenylamine Units for Energy Storage and Biological Applications

International journal of molecular sciences, 2023-05, Vol.24 (10), p.8966 [Peer Reviewed Journal]

COPYRIGHT 2023 MDPI AG ;2023 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. ;2023 by the authors. 2023 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms24108966 ;PMID: 37240313

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11
Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond
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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12
Recent Advances in the Synthesis and Applications of m-Aryloxy Phenols
Recent Advances in the Synthesis and Applications of m-Aryloxy Phenols
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Article 		Add to My Research

Recent Advances in the Synthesis and Applications of m-Aryloxy Phenols

Molecules (Basel, Switzerland), 2023-03, Vol.28 (6), p.2657 [Peer Reviewed Journal]

COPYRIGHT 2023 MDPI AG ;2023 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. ;2023 by the authors. 2023 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules28062657 ;PMID: 36985628

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13
Magnetic Pd-Fe3O4 Heterodimer Nanocrystals as Recoverable Catalysts for Ligand-Free Hiyama Cross-Coupling Reactions
Magnetic Pd-Fe3O4 Heterodimer Nanocrystals as Recoverable Catalysts for Ligand-Free Hiyama Cross-Coupling Reactions
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Magnetic Pd-Fe3O4 Heterodimer Nanocrystals as Recoverable Catalysts for Ligand-Free Hiyama Cross-Coupling Reactions

Bulletin of the Korean Chemical Society, 2016, 37(12), , pp.1992-1997 [Peer Reviewed Journal]

2016 Korean Chemical Society, Seoul & Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1229-5949 ;ISSN: 0253-2964 ;EISSN: 1229-5949 ;DOI: 10.1002/bkcs.11013

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14
Synthesis of New Azetidine and Oxetane Amino Acid Derivatives through Aza-Michael Addition of NH-Heterocycles with Methyl 2-(Azetidin- or Oxetan-3-Ylidene)Acetates
Synthesis of New Azetidine and Oxetane Amino Acid Derivatives through Aza-Michael Addition of NH-Heterocycles with Methyl 2-(Azetidin- or Oxetan-3-Ylidene)Acetates
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Synthesis of New Azetidine and Oxetane Amino Acid Derivatives through Aza-Michael Addition of NH-Heterocycles with Methyl 2-(Azetidin- or Oxetan-3-Ylidene)Acetates

Molecules (Basel, Switzerland), 2023-01, Vol.28 (3), p.1091 [Peer Reviewed Journal]

COPYRIGHT 2023 MDPI AG ;2023 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. ;2023 by the authors. 2023 ;ISSN: 1420-3049 ;EISSN: 1420-3049 ;DOI: 10.3390/molecules28031091 ;PMID: 36770762

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15
Phosphine-incorporated Metal-Organic Framework for Palladium Catalyzed Heck Coupling Reaction
Phosphine-incorporated Metal-Organic Framework for Palladium Catalyzed Heck Coupling Reaction
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Phosphine-incorporated Metal-Organic Framework for Palladium Catalyzed Heck Coupling Reaction

ChemistryOpen (Weinheim), 2024-04, p.e202300249-e202300249 [Peer Reviewed Journal]

2024 The Authors. ChemistryOpen published by Wiley-VCH GmbH. ;EISSN: 2191-1363 ;DOI: 10.1002/open.202300249 ;PMID: 38593358

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16
New Allosteric Modulators of AMPA Receptors: Synthesis and Study of Their Functional Activity by Radioligand-Receptor Binding Analysis
New Allosteric Modulators of AMPA Receptors: Synthesis and Study of Their Functional Activity by Radioligand-Receptor Binding Analysis
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Article 		Add to My Research

New Allosteric Modulators of AMPA Receptors: Synthesis and Study of Their Functional Activity by Radioligand-Receptor Binding Analysis

International journal of molecular sciences, 2023-06, Vol.24 (12), p.10293 [Peer Reviewed Journal]

COPYRIGHT 2023 MDPI AG ;2023 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. ;2023 by the authors. 2023 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms241210293 ;PMID: 37373440

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17
Recent Advances in Microwave-Assisted Copper-Catalyzed Cross-Coupling Reactions
Recent Advances in Microwave-Assisted Copper-Catalyzed Cross-Coupling Reactions
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Recent Advances in Microwave-Assisted Copper-Catalyzed Cross-Coupling Reactions

Catalysts, 2021-01, Vol.11 (1), p.46 [Peer Reviewed Journal]

2021. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). 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/catal11010046

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18
Preparation of Synthetic and Natural Derivatives of Flavonoids Using Suzuki-Miyaura Cross-Coupling Reaction
Preparation of Synthetic and Natural Derivatives of Flavonoids Using Suzuki-Miyaura Cross-Coupling Reaction
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Article 		Add to My Research

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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19
N,N-Bis(4′-(hexyloxy)-[1,1′-biphenyl]-4-yl)thiophen-2-amine
N,N-Bis(4′-(hexyloxy)-[1,1′-biphenyl]-4-yl)thiophen-2-amine
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N,N-Bis(4′-(hexyloxy)-[1,1′-biphenyl]-4-yl)thiophen-2-amine

MolBank, 2021-12, Vol.2021 (4), p.M1290 [Peer Reviewed Journal]

2021 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: 1422-8599 ;EISSN: 1422-8599 ;DOI: 10.3390/M1290

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20
Palladium Mesoionic Carbene Pre-catalyst for General Cross-Coupling Transformations in Deep Eutectic Solvents
Palladium Mesoionic Carbene Pre-catalyst for General Cross-Coupling Transformations in Deep Eutectic Solvents
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Article 		Add to My Research

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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