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Published in 2018 at "Catalysis Surveys from Asia"
DOI: 10.1007/s10563-018-9245-6
Abstract: The graphene supported Cu2O nanoparticles were prepared via a two-step liquid-phase method and exhibited high catalytic activity and stability for the Ullmann coupling of aryl halides with N–H containing compounds under mild and ligand-free conditions.…
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Keywords:
ligand free;
containing compounds;
cu2o graphene;
aryl halides ... See more keywords
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Published in 2020 at "International journal of biological macromolecules"
DOI: 10.1016/j.ijbiomac.2020.01.157
Abstract: This work reports i) green synthesis of palladium nanoparticles (Pd NPs) on the developed biodegradable microbeads as stabilizers, featuring chitosan, agarose and beta-cyclodextrin, ii) investigation of the catalytic role of the Pd NPs prepared in…
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Keywords:
palladium nanoparticles;
developed biodegradable;
cyanation;
biodegradable microbeads ... See more keywords
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Published in 2017 at "Tetrahedron Letters"
DOI: 10.1016/j.tetlet.2017.03.016
Abstract: Transition-metal-free hydrodehalogenation of aryl halides (eg. bromides) can take place efficiently in the presence of green polyethylene glycol (PEG-800) and t-BuOK without adding any extra solvents and additives. A radical mechanism is proposed for this…
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Keywords:
hydrodehalogenation aryl;
glycol peg;
polyethylene glycol;
aryl halides ... See more keywords
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2
Published in 2022 at "Inorganic chemistry"
DOI: 10.1021/acs.inorgchem.2c02385
Abstract: Transition-metal-catalyzed amination of aryl halides is a useful approach for the synthesis of medicinal compounds, organic functional materials, and agrochemical compounds. A systematic DFT study has been performed to investigate the mechanism of the Co(I)-catalyzed…
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Keywords:
aryl halides;
catalyzed amination;
amination;
amination aryl ... See more keywords
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Published in 2020 at "Organic letters"
DOI: 10.1021/acs.orglett.0c03069
Abstract: Boric acid, B(OH)3, is proved to be an efficient hydroxide reagent in converting (hetero)aryl halides to the corresponding phenols with a Pd catalyst under mild conditions. Various phenol products were obtained in good to excellent…
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Keywords:
catalyzed hydroxylation;
palladium catalyzed;
aryl halides;
hydroxylation aryl ... See more keywords
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1
Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c02358
Abstract: Aromatic halides constitute a valuable class of building blocks that are commonly used in organic synthesis. In this study, we demonstrate usage of aryl bromides and aryl iodides in C-Br or C-I bond formation. Methyl…
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Keywords:
tethered diols;
bromination iodination;
arene tethered;
aryl halides ... See more keywords
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1
Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c02631
Abstract: We report the synthesis of aryl boronic esters and aryl phosphonate esters promoted by visible-light in the absence of transition-metals or photoredox catalysts. The transformation proceeds at room temperature using sodium hydride, as a non-nucleophilic…
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Keywords:
enable photoinduced;
aryl halides;
eda;
photoinduced borylation ... See more keywords
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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c03840
Abstract: A highly efficient hydroxylation of (hetero)aryl halides using water as a hydroxyl source via Ni catalysis promoted by PhSiH3 under thermal catalysis is reported. This methodology provides a general procedure to obtain diverse multifunctional pharmaceutically…
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Keywords:
catalysis;
thermal catalysis;
aryl halides;
water ... See more keywords
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2
Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.2c04210
Abstract: A general strategy for the construction of dual-functional carbon-heteroatom bonds has been developed via a light-promoted nickel catalytic system. Employing a simple NiBr2 as the catalyst without any exogeneous ligands and photosensitizers, a variety of…
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Keywords:
promoted nickel;
coupling aryl;
nickel catalyzed;
aryl halides ... See more keywords
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2
Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.3c01147
Abstract: An efficient photoredox/nickel dual-catalyzed coupling of allyl trifluoroborates with aryl halides has been developed, which provides an attractive route to diverse-substituted allylic benzenes. The method offers several advantages, such as high efficiency and regioselectivity, mild…
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Keywords:
trifluoroborates aryl;
allyl trifluoroborates;
aryl halides;
dual catalyzed ... See more keywords
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Published in 2017 at "Organic letters"
DOI: 10.1021/acs.orglett.7b00111
Abstract: A palladium-catalyzed, three-component reaction between propargylic alcohols, CO2, and aryl halides was developed whereby a sequential carboxylation, trans-oxopalladation of the C≡C bond by an ArPdX species, and a reductive elimination procedure afforded a series of…
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Keywords:
functionalized alkylidene;
palladium catalyzed;
propargylic alcohols;
aryl halides ... See more keywords