Articles with "light photoredox" as a keyword



Visible-light-photoredox catalytic CC, CN bond formation: Synthesis of pyrazole derivatives via radical ions

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Published in 2017 at "Catalysis Communications"

DOI: 10.1016/j.catcom.2017.06.051

Abstract: Abstract A new approach for 5-amino-pyrazole-4-carbonitriles has been developed employing visible light photoredox catalysis. The green attributes of our work exploit on the utilization of visible light and Eosin Y organo photocatalyst as inexpensive, non-toxic,… read more here.

Keywords: light photoredox; visible light; formation; catalytic bond ... See more keywords
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Visible-light photoredox catalyzed cyclization of aryl alkynoates for the synthesis of trifluoromethylated coumarins

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Published in 2018 at "Catalysis Communications"

DOI: 10.1016/j.catcom.2018.06.009

Abstract: Abstract A strategy for the synthesis of coumarin derivatives via visible-light photoredox catalysis has been developed using fac-Ir(ppy)3 as the photocatalyst under mild conditions. Trifluoromethanesulfonyl chloride is utilized as the trifluoromethylation reagent, which is cheap… read more here.

Keywords: cyclization; light photoredox; visible light; photoredox catalyzed ... See more keywords
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Regioselective oxidative ring-opening of cyclopropenyl carboxylates by visible light photoredox catalysis

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Published in 2018 at "Tetrahedron Letters"

DOI: 10.1016/j.tetlet.2018.05.047

Abstract: Abstract Catalyzed by Ir(dFCF 3 ppy) 2 (dtbbpy)PF 6 , several aroyl methylidenemalonates were synthesized in good to excellent yields via visible light photoredox-catalyzed the oxidative ring-opening of cyclopropenyl carboxylate derivatives. The possible mechanism of… read more here.

Keywords: ring opening; oxidative ring; opening cyclopropenyl; light photoredox ... See more keywords
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Alcohol Etherification via Alkoxy Radicals Generated by Visible-Light Photoredox Catalysis

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Published in 2020 at "Organic Letters"

DOI: 10.1021/acs.orglett.0c03058

Abstract: A mechanistically divergent method is described that, employing a commercially available hypervalent iodine(III) reagent, generates alkoxy radicals from 1°, 2°, and 3° alcohols and allows their use in the functionalization of C(sp3)–H and C(sp2)–H bonds.… read more here.

Keywords: alkoxy radicals; photoredox catalysis; light photoredox; visible light ... See more keywords

An I2-Catalyzed, Visible-Light Photoredox-Mediated Radical Conversion of α-Nitrocarbonyls to Nitrile Oxides: Catalytic Access to Isoxazolines and Isoxazoles from Alkenes and Alkynes.

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Published in 2025 at "Organic letters"

DOI: 10.1021/acs.orglett.5c04111

Abstract: A visible light-mediated, I2-catalyzed intermolecular transformation of alkenes, conjugated dienes, styrenes, and alkynes to isoxazolines and isoxazoles with α-nitrocarbonyls is reported. The reaction is also applicable to 1,1-disubstituted terminal, 1,2-disubstituted internal and trisubstituted alkenes, and… read more here.

Keywords: isoxazolines isoxazoles; light photoredox; visible light; conversion ... See more keywords

Radical Sulfimidation via Visible-Light Photoredox Catalysis: N-Acyloxyamides as Bench-Stable Nitrene Surrogates.

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Published in 2025 at "Organic letters"

DOI: 10.1021/acs.orglett.5c04127

Abstract: Herein, we describe a visible-light-driven sulfimidation of thioethers with N-acyloxyamides catalyzed by TPT. The protocol proceeds under ambient conditions, tolerates a broad range of functional groups, and delivers the desired products in yields of up… read more here.

Keywords: sulfimidation; radical sulfimidation; light photoredox; visible light ... See more keywords
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Synthesis of 4-Isoxazolines via Visible-Light Photoredox-Catalyzed [3 + 2] Cycloaddition of Oxaziridines with Alkynes.

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Published in 2017 at "Organic letters"

DOI: 10.1021/acs.orglett.7b03369

Abstract: A method for [3 + 2] cycloaddition of oxaziridines with alkynes to form 4-isoxazolines via visible-light photoredox catalysis is described. This method is a greener, atom-economical reaction that tolerates various functional groups and provides good… read more here.

Keywords: cycloaddition oxaziridines; oxaziridines alkynes; visible light; light photoredox ... See more keywords
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Visible-Light Photoredox/Nickel Dual Catalysis for the Cross-Coupling of Sulfinic Acid Salts with Aryl Iodides.

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Published in 2018 at "Organic letters"

DOI: 10.1021/acs.orglett.7b03896

Abstract: An efficient cross-coupling of sodium or lithium sulfinates with aryl iodides, using a combination of nickel and photoredox catalysis, is described. The dual catalyst system enables a versatile synthesis of aryl sulfones at room temperature… read more here.

Keywords: light photoredox; aryl iodides; catalysis; visible light ... See more keywords

Visible-Light Photoredox-Catalyzed Iminyl Radical Formation by N-H Cleavage with Hydrogen Release and Its Application in Synthesis of Isoquinolines.

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Published in 2018 at "Organic letters"

DOI: 10.1021/acs.orglett.8b00193

Abstract: An unprecedented visible-light photoredox-catalyzed iminyl radical formation by N-H cleavage with H2 release has been developed. Its application in the synthesis of various isoquinolines and related polyaromatics in high atom economy at ambient temperature by… read more here.

Keywords: iminyl radical; light photoredox; visible light; catalyzed iminyl ... See more keywords
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Visible-Light Photoredox-Catalyzed Hydroalkoxymethylation of Activated Alkenes Using α-Silyl Ethers as Alkoxymethyl Radical Equivalents.

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Published in 2018 at "Organic letters"

DOI: 10.1021/acs.orglett.8b02721

Abstract: A new neutral silicon-based traceless activation group (TAG) for visible-light photoredox-catalyzed hydroalkoxymethylation of alkenes is presented. This reaction involves in-situ-generated alkoxymethyl radical via single electron oxidation (SET) of α-TMS-substituted ethers, followed by subsequent conjugate addition… read more here.

Keywords: alkoxymethyl radical; light photoredox; visible light; activated alkenes ... See more keywords

Photocatalyst-Free Visible-Light Photoredox Dearomatization of Phenol Derivatives Containing Ketoximes: An Easy Access to Spiropyrrolines.

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Published in 2019 at "Organic letters"

DOI: 10.1021/acs.orglett.9b00372

Abstract: A novel and simple visible-light photoredox intramolecular dearomatization of phenol derivatives containing ketoximes leading to spiropyrrolines has been developed. The protocol uses readily available 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) as the base and electron-donor, visible light as the… read more here.

Keywords: phenol derivatives; dearomatization phenol; light photoredox; visible light ... See more keywords