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[1]
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ppm level supported Pd-catalyzed carbonylative Suzuki–Miyaura cross-coupling of aryl iodides using oxalic acid as CO source
Molecular Catalysis,
2023
DOI:10.1016/j.mcat.2023.113546
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[2]
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Tetra- and Dinuclear Palladium Complexes Based on a Ligand of 2,8-Di-2-pyridinylanthyridine: Preparation, Characterization, and Catalytic Activity
Organometallics,
2021
DOI:10.1021/acs.organomet.1c00226
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[3]
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Advances in Transition‐Metal Catalyzed Carbonylative Suzuki‐Miyaura Coupling Reaction: An Update
Advanced Synthesis & Catalysis,
2021
DOI:10.1002/adsc.202001509
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[4]
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Advances in Transition‐Metal Catalyzed Carbonylative Suzuki‐Miyaura Coupling Reaction: An Update
Advanced Synthesis & Catalysis,
2021
DOI:10.1002/adsc.202001509
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[5]
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Tetra- and Dinuclear Palladium Complexes Based on a Ligand of 2,8-Di-2-pyridinylanthyridine: Preparation, Characterization, and Catalytic Activity
Organometallics,
2021
DOI:10.1021/acs.organomet.1c00226
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[6]
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Novel and efficient bridged bis(
N
‐heterocyclic carbene)palladium(II) catalysts for selective carbonylative Suzuki–Miyaura coupling reactions to biaryl ketones and biaryl diketones
Applied Organometallic Chemistry,
2020
DOI:10.1002/aoc.5636
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[7]
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Novel and efficient bridged bis(N‐heterocyclic carbene)palladium(II) catalysts for selective carbonylative Suzuki–Miyaura coupling reactions to biaryl ketones and biaryl diketones
Applied Organometallic Chemistry,
2020
DOI:10.1002/aoc.5636
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[8]
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“CO” as a Carbon Bridge to Build Complex C2-Branched Glycosides Using a Palladium-Catalyzed Carbonylative Suzuki–Miyaura Reaction from 2-Iodoglycals
The Journal of Organic Chemistry,
2019
DOI:10.1021/acs.joc.8b03248
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[9]
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“CO” as a Carbon Bridge to Build Complex C2-Branched Glycosides Using a Palladium-Catalyzed Carbonylative Suzuki–Miyaura Reaction from 2-Iodoglycals
The Journal of Organic Chemistry,
2019
DOI:10.1021/acs.joc.8b03248
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[10]
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Pd‐NHC catalysed Carbonylative Suzuki coupling reaction and its application towards the synthesis of biologically active 3‐aroylquinolin‐4 (1H)‐one and acridone scaffolds
Applied Organometallic Chemistry,
2018
DOI:10.1002/aoc.4173
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[11]
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Palladium Catalyzed Carbonylative Coupling for Synthesis of Arylketones and Arylesters Using Chloroform as the Carbon Monoxide Source
The Journal of Organic Chemistry,
2017
DOI:10.1021/acs.joc.6b02711
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[12]
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Palladium Catalyzed Carbonylative Coupling for Synthesis of Arylketones and Arylesters Using Chloroform as the Carbon Monoxide Source
The Journal of Organic Chemistry,
2017
DOI:10.1021/acs.joc.6b02711
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[13]
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Pd-NHC catalysed Carbonylative Suzuki coupling reaction and its application towards the synthesis of biologically active 3-aroylquinolin-4 (1H
)-one and acridone scaffolds
Applied Organometallic Chemistry,
2017
DOI:10.1002/aoc.4173
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[14]
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Carbonylative Suzuki–Miyaura coupling catalyzed by palladium supported on aminopropyl polymethylsiloxane microspheres under atmospheric pressure of CO
Journal of Molecular Catalysis A: Chemical,
2016
DOI:10.1016/j.molcata.2016.03.017
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[15]
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Biaryl Diketone Synthesis via Palladium-catalyzed Carbonylative Coupling with Carbon Monoxide or Various Metal Carbonyls
Bulletin of the Korean Chemical Society,
2016
DOI:10.1002/bkcs.10904
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[16]
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Biaryl Diketone Synthesis via Palladium‐catalyzed Carbonylative Coupling with Carbon Monoxide or Various Metal Carbonyls
Bulletin of the Korean Chemical Society,
2016
DOI:10.1002/bkcs.10904
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