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      Photocatalytic Difluoromethylation Reactions of Aromatic Compounds and Aliphatic Multiple C–C Bonds

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          Abstract

          Among the realm of visible light photocatalytic transformations, late-stage difluoromethylation reactions (introduction of difluoromethyl groups in the last stages of synthetic protocols) have played relevant roles as the CF 2X group substitutions exert positive impacts on the physical properties of organic compounds including solubility, metabolic stability, and lipophilicity, which are tenets of considerable importance in pharmaceutical, agrochemical, and materials science. Visible-light-photocatalyzed difluoromethylation reactions are shown to be accomplished on (hetero)aromatic and carbon–carbon unsaturated aliphatic substrates under mild and environmentally benign conditions.

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          Visible light photoredox catalysis with transition metal complexes: applications in organic synthesis.

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            Organic Photoredox Catalysis.

            In this review, we highlight the use of organic photoredox catalysts in a myriad of synthetic transformations with a range of applications. This overview is arranged by catalyst class where the photophysics and electrochemical characteristics of each is discussed to underscore the differences and advantages to each type of single electron redox agent. We highlight both net reductive and oxidative as well as redox neutral transformations that can be accomplished using purely organic photoredox-active catalysts. An overview of the basic photophysics and electron transfer theory is presented in order to provide a comprehensive guide for employing this class of catalysts in photoredox manifolds.
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              Visible-Light Photocatalysis: Does It Make a Difference in Organic Synthesis?

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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Molecules
                Molecules
                molecules
                Molecules
                MDPI
                1420-3049
                06 December 2019
                December 2019
                : 24
                : 24
                : 4483
                Affiliations
                Universidad de Buenos Aires, Facultad de Farmacia y Bioquímica, Departamento de Química Orgánica, Junín 954, Buenos Aires CP1113, Argentina; sbaratavallejo@ 123456ffyb.uba.ar
                Author notes
                [* ]Correspondence: apostigo@ 123456ffyb.uba.ar
                Article
                molecules-24-04483
                10.3390/molecules24244483
                6943576
                31817797
                e090f658-1ac9-4450-9d3d-500d06872f30
                © 2019 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 18 November 2019
                : 05 December 2019
                Categories
                Review

                difluoromethylation,photocatalytic difluoromethylation,visible light,difluoromethyl-substituted (hetero)arenes,difluoromethylation of olefins

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