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Published in 2020 at "Organic letters"
DOI: 10.1021/acs.orglett.0c01683
Abstract: Allylboronates are unique building blocks widely used in organic synthesis, but the construction of cyclic allylboranates remains a challenging subject. We demonstrate here a mild and efficient access to this type of compound through the…
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Keywords:
allylboronates vinyl;
triflates chloroboronates;
nickel catalysis;
chloroboronates reductive ... See more keywords
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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…
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Keywords:
butadiene;
nickel catalysis;
merging photoredox;
photoredox nickel ... See more keywords
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Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.2c04228
Abstract: We present a novel nickel-catalyzed reaction of indole-tethered 2-alkynylphenol esters with various (hetero)aryl boronic acids, resulting in the synthesis of diversely functionalized pentacyclic benzofurocyclohepta[b]indole derivatives. This unprecedented cascade reaction involves the arylative cyclization of alkynes,…
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Keywords:
nickel catalysis;
construction pentacyclic;
framework enabled;
enabled nickel ... See more keywords
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Published in 2022 at "Journal of the American Chemical Society"
DOI: 10.1021/jacs.2c03220
Abstract: Introducing the novel concept of amino radical transfer (ART) enables the use of easily accessible and commercially available alkyl boronic esters as cross-coupling partners for aryl halides in dual photoredox/nickel catalysis mediated by visible light.…
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Keywords:
radical transfer;
sp2 sp3;
nickel catalysis;
amino radical ... See more keywords
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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…
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Keywords:
internal alkynes;
nickel catalysis;
via photoredox;
site stereoselective ... See more keywords
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Published in 2017 at "Journal of the American Chemical Society"
DOI: 10.1021/jacs.7b02326
Abstract: In this article a successful protocol was developed to construct carbon-carbon bonds by the extrusion of the O atom of ethers via nickel catalysis in the presence of reductants. This methodology is featured as a…
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Keywords:
carbon bonds;
nickel catalysis;
carbon;
carbon carbon ... See more keywords
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Published in 2020 at "Nature"
DOI: 10.1038/s41586-020-2701-2
Abstract: Strained cyclic organic molecules, such as arynes, cyclic alkynes and cyclic allenes, have intrigued chemists for more than a century with their unusual structures and high chemical reactivity 1 . The considerable ring strain (30–50…
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Keywords:
nickel catalysis;
absolute stereochemistry;
allene;
asymmetric nickel ... See more keywords
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1
Published in 2022 at "Chemical communications"
DOI: 10.1039/d2cc04408k
Abstract: Herein, we describe a protocol for the direct and selective acylation and alkynylation of the C(sp3)-H bonds of saturated hydrocarbons by synergistic decatungstate photo-HAT and nickel catalysis. This method, using cheap and easy-to-synthesize TBADT as…
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Keywords:
decatungstate photo;
synergistic decatungstate;
nickel catalysis;
hat nickel ... See more keywords