Results 91 to 100 of about 482,822 (233)

Lutetium texaphyrin: A photocatalyst that triggers pyroptosis via biomolecular photoredox catalysis

open access: yesProceedings of the National Academy of Sciences of the United States of America
Significance Photon-controlled pyroptosis activation (PhotoPyro) holds promise for cancer immunotherapy by selectively triggering cell death. Here, we report that biomolecular photoredox catalysis in cells contributes to PhotoPyro.
Yun-Jie Xu   +8 more
semanticscholar   +1 more source

The dark side of photocatalysis: near-infrared photoredox catalysis for organic synthesis

open access: yes, 2021
Near-Infrared photoredox catalysis is now consider as the next evolution of this field. Photoredox catalysis is now considered as a major topic in the field of organic synthesis.
Cormier, Morgan   +2 more
core   +1 more source

Deal;Photoredox Catalysis for the Cycloaddition Reactions

open access: yesChemCatChem, 2020
AbstractCycloaddition reaction is a powerful tool for the synthesis of cyclic structures in a green way. High‐energy ultraviolet (UV) light was strictly required for the traditional photochemical processes. However, in the past ten years, discovery of photoredox catalysis for the cycloaddition reactions have attracted significant attention.
Tong Zhang, Yu Zhang, Shoubhik Das
openaire   +3 more sources

Switching on elusive organometallic mechanisms with photoredox catalysis [PDF]

open access: yesNature, 2015
Transition-metal-catalysed cross-coupling reactions have become one of the most used carbon-carbon and carbon-heteroatom bond-forming reactions in chemical synthesis. Recently, nickel catalysis has been shown to participate in a wide variety of C-C bond-forming reactions, most notably Negishi, Suzuki-Miyaura, Stille, Kumada and Hiyama couplings ...
Jack A. Terrett   +3 more
openaire   +2 more sources

Photoredox-Catalyzed Hydroxymethylation of Heteroaromatic Bases

open access: yes, 2016
We report the development of a method for room-temperature C–H hydroxymethylation of heteroarenes. A key enabling advance in this work was achieved by implementing visible light photoredox catalysis that proved to be applicable to many classes of ...
Ryan D. Cohen (1458091)   +5 more
core   +1 more source

A Multiphoton Single-Electron Reduction of Olefins via Tandem Photoredox Catalysis [PDF]

open access: yes, 2020
Herein we report a visible light multiphoton tandem photoredox catalysis strategy enabling a distinctive mode of olefin activation via a one electron reduction to the corresponding radical anion.
Anastasios, Polyzos   +3 more
core   +3 more sources

A modern approach to intermittent illumination for the characterization of chain-propagation in photoredox catalysis

open access: yesTetrahedron Chem
Photoredox catalysis has become an invaluable tool for the construction of organic molecules, allowing for unparalleled control over radical intermediates enabled by the mild conditions achieved through visible-light activation of a photocatalyst.
K.A. Viraj Miyuranga   +2 more
doaj   +1 more source

Asymmetric 1,4-functionalization of 1,3-enynes via dual photoredox and chromium catalysis

open access: yesNature Communications, 2022
In contrast to the better-studied ionic pathway, radical-involved asymmetric 1,4-functionalization of 1,3-enynes remains a prominent challenge. Here, the authors describe the asymmetric three-component 1,4-dialkylation of 1,3-enynes via dual photoredox ...
Feng-Hua Zhang   +3 more
doaj   +1 more source

Double-shelled hollow rods assembled from nitrogen/sulfur-codoped carbon coated indium oxide nanoparticles as excellent photocatalysts

open access: yesNature Communications, 2019
While photoredox catalysis presents exciting avenues for molecular transformations, balancing optimal photochemical and materials properties can be challenging. Here, the authors prepare carbon-coated In2O3 nanoparticles as recoverable photocatalysts for
Liming Sun   +6 more
doaj   +1 more source

Decarboxylative C(sp3)–N cross-coupling via synergetic photoredox and copper catalysis [PDF]

open access: yes
Amines are a quintessential moiety in bioactive molecules, pharmaceuticals and organic materials. Transition-metal-catalysed C–N coupling of aryl electrophiles has been established as a powerful and reliable method for amine synthesis.
Frey, Adrian   +3 more
core   +3 more sources

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