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Published in 2022 at "Inorganic chemistry"
DOI: 10.1021/acs.inorgchem.1c03961
Abstract: We report herein an exploration of the straightforward one-pot dual-catalysis strategy, i.e., direct combination of a photoactive coordination polymer (CP) with another metal catalyst, for carrying out the desirable photoinduced organic transformation. The strategy overcomes…
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Keywords:
reaction;
dual catalysis;
pot dual;
one pot ... See more keywords
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Published in 2021 at "Organic letters"
DOI: 10.1021/acs.orglett.1c00189
Abstract: We describe an efficient photoredox system, relying on decatungstate/disulfide catalysts, for the hydrofunctionalization of styrenes. In this methodology the use of disulfide as a cocatalyst was shown to be crucial for the reaction efficiency. This…
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Keywords:
disulfide dual;
disulfide;
visible light;
decatungstate disulfide ... See more keywords
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1
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…
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Keywords:
sp3;
dual catalysis;
photoredox nickel;
cyclopropanes via ... See more keywords
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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c00969
Abstract: The development of mild and practical conditions for the fluoroalkylation of arenes is an ongoing challenge in chemical organic synthesis. Herein, we report a metallaphotoredox method for the preparation of fluoroalkyl arenes based on the…
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Keywords:
catalysis;
synthesis fluorinated;
dual catalysis;
copper dual ... See more keywords
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1
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…
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Keywords:
unactivated alkene;
dicarbofunctionalizations unactivated;
dual catalysis;
photoredox nickel ... See more keywords
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1
Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c03481
Abstract: Hydroacylation of alkynes is undoubtedly the simplest and most atom-efficient approach for the synthesis of enones with diverse synthetic applications. Despite significant progress in hydroacylations, no hydroacylations exist that make use of aldehydes without a…
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Keywords:
hydroacylation;
catalysis chelation;
dual catalysis;
terminal alkynes ... See more keywords
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Published in 2019 at "Journal of the American Chemical Society"
DOI: 10.1021/jacs.9b08282
Abstract: An intermolecular, photocatalytic dicarbofunctionalization (DCF) of olefins enabled by the merger of Giese-type addition with Ni/photoredox dual catalysis has been realized. Capitalizing on the rapid addition of 3° radicals to alkenes and their reluctance toward…
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Keywords:
olefin;
photoredox dual;
three component;
dicarbofunctionalization ... See more keywords
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Published in 2019 at "Chemical communications"
DOI: 10.1039/c9cc00493a
Abstract: A dual catalysis system was developed to synthesize hydrolyzable polyether-polyester copolymers from propylene oxide and cyclic esters such as γ-butyrolactone, δ-valerolactone, and ε-caprolactone. A bimetallic chromium catalyst active for the enantioselective polymerisation of propylene oxide…
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Keywords:
catalysis copolymerisation;
epoxides lactones;
catalysis;
copolymerisation epoxides ... See more keywords
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Published in 2019 at "Chemical communications"
DOI: 10.1039/c9cc08559a
Abstract: A relay Rh(ii)/Pd(0) dual catalysis that enables domino [1,2]-sigmatropic rearrangement/allylic alkylation of α-diazo tertiary alcohols is described. This transformation represents a highly efficient method for the one-pot synthesis of α-quaternary β-keto-esters under mild conditions, in…
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Keywords:
diazo tertiary;
relay dual;
sigmatropic rearrangement;
allylic alkylation ... See more keywords
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Published in 2022 at "Chemical communications"
DOI: 10.1039/d2cc03595b
Abstract: An enantioselective ortho-C(sp2)-H functionalization of ketones with 1,6-enynes is demonstrated via photoredox/cobalt dual catalysis. The method exhibits high yields, functional group tolerance, and selectivity. Mechanistic studies suggested the operation of visible-light mediated low-valent cobalt complex…
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Keywords:
cobalt;
via photoredox;
ketones enynes;
dual catalysis ... See more keywords
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2
Published in 2023 at "Chemical Science"
DOI: 10.1039/d2sc06303d
Abstract: A three-component reductive cross-coupling of aryl halides, aldehydes, and alkenes by nickel/photoredox dual catalysis is disclosed. The key to success for this tandem transformation is to identify α-silylamine as a unique organic reductant, which releases…
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Keywords:
conjugate addition;
component reductive;
dual catalysis;
photoredox dual ... See more keywords