Articles with "photoredox nickel" as a keyword



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Ti(OiPr)4-Enabled Dual Photoredox and Nickel-Catalyzed Arylation and Alkenylation of Cyclopropanols.

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Published in 2021 at "Organic letters"

DOI: 10.1021/acs.orglett.1c01795

Abstract: Readily available from esters or ketones, cyclopropanols are inclined to undergo diverse ring-opening transformations. Their one-electron oxidation is a conventional way to β-carbonyl radicals. However, despite this fact, their application as a coupling partner in… read more here.

Keywords: photoredox nickel; oipr enabled; nickel catalyzed; dual photoredox ... See more keywords
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Photoredox/Nickel Dual Catalysis Enables the Synthesis of Alkyl Cyclopropanes via C(sp3)-C(sp3) Cross Electrophile Coupling of Unactivated Alkyl Electrophiles.

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Published in 2022 at "Organic letters"

DOI: 10.1021/acs.orglett.1c04268

Abstract: A facile synthesis of mono-, 1,1- and 1,2-disubstituted cyclopropanes via visible light-mediated photoredox/nickel dual catalysis is demonstrated. The challenging intramolecular C(sp3)-C(sp3) cross-electrophile coupling of readily available unactivated 1,3-dialkyl electrophiles was performed under mild conditions that… read more here.

Keywords: sp3; dual catalysis; photoredox nickel; cyclopropanes via ... See more keywords
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Dicarbofunctionalizations of an Unactivated Alkene via Photoredox/Nickel Dual Catalysis.

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Published in 2022 at "Organic letters"

DOI: 10.1021/acs.orglett.2c02355

Abstract: 1,2-Dicarbofunctionalization of unactivated olefin has been reported under photoredox/nickel dual catalysis. The mildness of the visible-light-mediated reaction allows the use of various alkyl and aryl electrophiles with several sensitive functional groups. The protocol was equally… read more here.

Keywords: unactivated alkene; dicarbofunctionalizations unactivated; dual catalysis; photoredox nickel ... See more keywords
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Redox-Neutral 1,4-Dicarbonfunctionalization of 1,3-Butadiene by Merging Photoredox and Nickel Catalysis.

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Published in 2022 at "Organic letters"

DOI: 10.1021/acs.orglett.2c04060

Abstract: The diverse functionalization of 1,3-butadiene provides wide applicability toward the synthesis of abundant and useful allylic compounds. Here, we describe a three-component and redox-neutral assembly of readily available C═X compounds, 1,3-butadiene, and various nucleophiles by… read more here.

Keywords: butadiene; nickel catalysis; merging photoredox; photoredox nickel ... See more keywords
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Photoredox/Nickel Dual-Catalyzed Regioselective Allylic Arylations of Allyl Trifluoroborates with Aryl Halides.

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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… read more here.

Keywords: trifluoroborates aryl; allyl trifluoroborates; aryl halides; dual catalyzed ... See more keywords
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Dual Photoredox/Nickel-Catalyzed Conversion of Aryl Halides to Aryl Aminooxetanes: Computational Evidence for a Substrate-Dependent Switch in Mechanism

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Published in 2019 at "ACS Catalysis"

DOI: 10.1021/acscatal.9b03596

Abstract: A mild and direct strategy for the construction of aryl aminooxetanes has been accomplished through the synergistic combination of photoredox and nickel catalysis. This approach represents a rare example of harnessing challenging tertiary radicals in… read more here.

Keywords: photoredox nickel; aryl aminooxetanes; photoredox; nickel catalyzed ... See more keywords
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Synthesis of C6-Substituted Purine Nucleoside Analogues via Late-Stage Photoredox/Nickel Dual Catalytic Cross-Coupling.

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Published in 2021 at "ACS medicinal chemistry letters"

DOI: 10.1021/acsmedchemlett.0c00673

Abstract: Nucleoside analogues have been and continue to be extremely important compounds in drug discovery. Despite the significant effort dedicated to their synthesis, medicinal chemistry campaigns around these structures are often hampered by synthetic challenges. We… read more here.

Keywords: photoredox nickel; medicinal chemistry; chemistry; nucleoside analogues ... See more keywords
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Site- and Stereoselective Synthesis of Alkenyl Chlorides by Dual Functionalization of Internal Alkynes via Photoredox/Nickel Catalysis.

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Published in 2023 at "Journal of the American Chemical Society"

DOI: 10.1021/jacs.3c02748

Abstract: Herein, we report a redox-neutral and atom-economical protocol to synthesize valuable alkenyl chlorides from unactivated internal alkynes and abundant organochlorides via photoredox and nickel catalysis. This protocol enables the site- and stereoselective addition of organochlorides… read more here.

Keywords: internal alkynes; nickel catalysis; via photoredox; site stereoselective ... See more keywords
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Dual photoredox and nickel-catalyzed desymmetric C–O coupling reactions: visible light-mediated enantioselective synthesis of 1,4-benzodioxanes

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Published in 2018 at "Organic chemistry frontiers"

DOI: 10.1039/c8qo00805a

Abstract: 1,4-Benzodioxane widely exists as the core structure in many therapeutic agents and bioactive natural compounds. Hence, to access this kind of molecule, an enantioselective desymmetric C–O cross coupling reaction has been developed through dual visible… read more here.

Keywords: photoredox nickel; catalyzed desymmetric; dual photoredox; visible light ... See more keywords
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Recent advances in photoredox and nickel dual-catalyzed cascade reactions: pushing the boundaries of complexity

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Published in 2020 at "Chemical Science"

DOI: 10.1039/d0sc00712a

Abstract: Cascade reactions that produce multiple chemical bonds in one synthetic operation are important in the efficient construction of complex molecules. read more here.

Keywords: photoredox nickel; cascade reactions; nickel dual; cascade ... See more keywords
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Reductive hydrobenzylation of terminal alkynes via photoredox and nickel dual catalysis.

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Published in 2021 at "Chemical communications"

DOI: 10.1039/d1cc03668h

Abstract: A photoredox/nickel dual catalyzed reductive hydrobenzylation of alkynes and benzyl chlorides by employing alkyl amines as a stoichiometric reductant is described. This synergistic protocol proceeds via Markovnikov-selective migratory insertion of an alkyne into nickel hydride,… read more here.

Keywords: photoredox nickel; hydrobenzylation terminal; reductive hydrobenzylation; nickel dual ... See more keywords