Results 51 to 60 of about 482,822 (233)

Dicyanopyrazine: 10th Anniversary in Photoredox Catalysis. [PDF]

open access: yesChem Rec
The last decade unveiled dicyanopyrazine as a purely organic photocatalyst capable of initiating a variety of unprecedented photoredox transformations. The latest discoveries also pointed to a facile Mallory‐type photocyclization of the catalyst to quinoxaline‐2,3‐dicarbonitrile derivative, which proved to be the active catalytic species. Its principal
Burešová Z, Bureš F.
europepmc   +4 more sources

Direct allylic acylation via cross-coupling involving cooperative N‑heterocyclic carbene, hydrogen atom transfer, and photoredox catalysis

open access: yesNature Communications, 2023
Herein, we report a mild, operationally simple, multicatalytic method for the synthesis of β,γ-unsaturated ketones via allylic acylation of alkenes. Specifically, the method combines N‑heterocyclic carbene catalysis, hydrogen atom transfer catalysis, and
Xiao-Chen Wang   +6 more
semanticscholar   +1 more source

Photoredox catalysis harnessing oxygen-centered radicals [PDF]

open access: yes, 2020
Visible light provides an abundant and renewable source of energy with an ample capacity to mediate chemical transformations. Photoredox catalysis utilizes this energy for the generation of high-energy radical intermediates and strategically employs ...
Ondrejková, Alica   +8 more
core   +1 more source

Photons or Electrons? A Critical Comparison of Electrochemistry and Photoredox Catalysis for Organic Synthesis

open access: yesChemical Reviews, 2021
Redox processes are at the heart of synthetic methods that rely on either electrochemistry or photoredox catalysis, but how do electrochemistry and photoredox catalysis compare? Both approaches provide access to high energy intermediates (e.g.
Nicholas E. S. Tay   +2 more
semanticscholar   +1 more source

An anion-binding approach to enantioselective photoredox catalysis. [PDF]

open access: yesScience
Photoredox catalysis has emerged as a transformative strategy in synthetic chemistry, enabling a wide variety of valuable chemical reactions through generation of highly reactive radical ion intermediates. Pairing chiral counteranions with cation radical intermediates provides a potentially generalizable tool for controlling absolute stereochemistry in
Vojáčková P, Jacobsen EN.
europepmc   +3 more sources

Visible-Light Photoredox Catalysis in Water

open access: yesThe Journal of Organic Chemistry, 2022
The use of water in organic synthesis draws attention to its green chemistry features and its unique ability to unveil unconventional reactivities. Herein, literature about the use of water as a reaction medium under visible-light photocatalytic conditions is summarized in order to highlight challenges and opportunities.
Camilla Russo   +3 more
openaire   +4 more sources

Single-molecule photoredox catalysis

open access: yesChemical Science, 2019
Photocatalytic dehalogenation by a common dyestuff under aqueous conditions is driven by energy-additive absorption of two photons on the single-molecule level.
Josef Haimerl   +4 more
openaire   +3 more sources

Photo-induced oxidant-free oxidative C–H/N–H cross-coupling between arenes and azoles

open access: yesNature Communications, 2017
Functionalization of unactivated C–H bonds is an attractive strategy to introduce functionality without the need for pre-functionalized starting materials.
Linbin Niu   +5 more
doaj   +1 more source

Developing Organometallic Nucleophilic Reagents Via Photoredox Catalysis [PDF]

open access: yes, 2023
The addition of organometallic reagents to the carbonyl group represents a key transformation, both in academia and industry. Most of these transformations rely on a mechanism in which accessible and reactive halides are transformed into the ...
Cozzi P. G.   +4 more
core   +1 more source

Ligand-controlled stereodivergent alkenylation of alkynes to access functionalized trans- and cis-1,3-dienes

open access: yesNature Communications, 2023
The stereoselective synthesis of 1,3-dienes represents a challenge in organic synthesis. Here, the authors report a ligand-controlled stereodivergent access to both Z- and E-sulfonyl-1,3-dienes via photoredox and nickel catalysis.
Tianyu Long   +6 more
doaj   +1 more source

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