Results 21 to 30 of about 229,704 (190)

Organic synthesis using photoredox catalysis [PDF]

open access: yesBeilstein Journal of Organic Chemistry, 2014
Natural photosynthesis is a remarkable chemical machinery that enables our life on earth and delivers a constant stream of oxygen and organic biomass. We should acknowledge this fact with humbleness, especially because we have not been able yet to mimic this process in a reliable way even after decades of intense research.
Axel G. Griesbeck
doaj   +3 more sources

Hydroxyl-Diazomethylation of Alkenes via Photoredox Catalysis [PDF]

open access: yes, 2023
α-Diazoesters belong to significantly important carbenoid precursors in synthetic chemistry, diazomethylation-based difunctionalization of alkenes is highly valuable but remain nontrivial. Herein, we reported a general and modular approach for the direct
Haisheng, Xie   +7 more
core   +1 more source

Combined Photoredox and Carbene Catalysis for the Synthesis of Ketones from Carboxylic Acids [PDF]

open access: yes, 2020
Disclosed herein is the development of a novel single-electron reduction of acyl azoliums for the formation of ketones from carboxylic acids. Facile construction of the acyl azolium in situ followed by a radical-radical coupling was made possible using ...
Karl, Scheidt   +3 more
core   +1 more source

Oxidase reactions in photoredox catalysis

open access: yesChemical Society Reviews, 2021
This tutorial review highlights the distinctive mechanistic roles of and practical considerations regarding terminal oxidants in photocatalytic “oxidase”-type reactions.
Nicholas L. Reed, Tehshik P. Yoon
openaire   +3 more sources

RECENTES APLICAÇÕES EM SÍNTESE ORGÂNICA DE CATÁLISE FOTO REDOX MEDIADA POR LUZ VISÍVEL

open access: yesQuímica Nova, 2015
In the past few years, photoredox catalysis has become a powerful tool in the field of organic synthesis. Using this efficient method, it is possible to excite organic compounds from visible light and attain alternative mechanistic pathways for the ...
Angelina M. de Almeida   +2 more
doaj   +1 more source

Spin-Forbidden Excitation Enables Infrared Photoredox Catalysis [PDF]

open access: yes, 2020
We describe a new family of catalysts that undergo direct ground state singlet to excited state triplet excitation with IR light, leading to photoredox catalysis without the energy waste associated with intersystem crossing.
Martin, Eastgate   +8 more
core   +2 more sources

Activation of Alkyl Chlorides Enabled by Zirconocene and Photoredox Catalysis [PDF]

open access: yes, 2022
C–Cl bond cleavage of unactivated alkyl chlorides with zirconocene and photoredox catalysis has been achieved. The present protocol exhibited a broader scope of alkyl chlorides compared to the preceding methods with titanocene. This scope expansion could
Keisuke, Tanaka   +4 more
core   +2 more sources

Temperature‐Dependent Photoredox Catalysis for CO2 Reduction Coupled with Selective Benzyl Alcohol Oxidation over ZnIn2S4/In2O3 Heterostructure

open access: yesAdvanced Energy & Sustainability Research, 2023
CO2 reduction (CO2RR) with selective benzyl alcohol (BA) oxidation in a single photoredox reaction can simultaneously utilize photogenerated electrons and holes to realize efficient production of fuels and value‐added chemicals.
Jian Lei   +6 more
doaj   +1 more source

Merging Visible-Light-Photoredox and Nickel Catalysis [PDF]

open access: yes, 2020
A new combination: The merging of visible‐light‐photoredox catalysis and nickel catalysis has been successfully achieved for cross‐coupling reactions. The synthetic scope and limitations of the combination of nickel and photoredox catalysis for Csp3-Csp2
Vila Descals, Carlos
core   +1 more source

Functionalized Polyamine Synthesis with Photoredox Catalysis

open access: yesChemistry – A European Journal, 2023
Abstract Polyamines, such as putrescine and spermidine, are pivotal in various biological processes across living organisms. Despite their significance, structurally modified polyamines offer a less‐explored avenue for discovering bioactive compounds. The limitation is attributed to the synthetic difficulty of accessing functionalized
Yuta Makihara   +4 more
openaire   +2 more sources

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