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      Generation of Alkyl Radicals: From the Tyranny of Tin to the Photon Democracy

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      , ,
      Chemical Reviews
      American Chemical Society

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          Abstract

          Alkyl radicals are key intermediates in organic synthesis. Their classic generation from alkyl halides has a severe drawback due to the employment of toxic tin hydrides to the point that “flight from the tyranny of tin” in radical processes was considered for a long time an unavoidable issue. This review summarizes the main alternative approaches for the generation of unstabilized alkyl radicals, using photons as traceless promoters. The recent development in photochemical and photocatalyzed processes enabled the discovery of a plethora of new alkyl radical precursors, opening the world of radical chemistry to a broader community, thus allowing a new era of photon democracy.

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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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            Dual Catalysis Strategies in Photochemical Synthesis

            The interaction between an electronically excited photocatalyst and an organic molecule can result in the genertion of a diverse array of reactive intermediates that can be manipulated in a variety of ways to result in synthetically useful bond constructions. This Review summarizes dual-catalyst strategies that have been applied to synthetic photochemistry. Mechanistically distinct modes of photocatalysis are discussed, including photoinduced electron transfer, hydrogen atom transfer, and energy transfer. We focus upon the cooperative interactions of photocatalysts with redox mediators, Lewis and Brønsted acids, organocatalysts, enzymes, and transition metal complexes.
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              The merger of transition metal and photocatalysis

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                Author and article information

                Journal
                Chem Rev
                Chem Rev
                cr
                chreay
                Chemical Reviews
                American Chemical Society
                0009-2665
                1520-6890
                06 August 2020
                09 September 2020
                : 120
                : 17
                : 9790-9833
                Affiliations
                []Stratingh Institute for Chemistry, Center for Systems Chemistry University of Groningen , Nijenborgh 4, 9747 AG Groningen, The Netherlands
                []PhotoGreen Lab , Department of Chemistry, V. Le Taramelli 10, 27100 Pavia, Italy
                Author notes
                [* ]Email: fagnoni@ 123456unipv.it . Tel: +39 0382 987198. Fax: +39 0382 987323.
                Article
                10.1021/acs.chemrev.0c00278
                8009483
                32786419
                93e578fa-da83-4817-bb85-230d0b4f35c3

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 08 April 2020
                Categories
                Review
                Custom metadata
                cr0c00278
                cr0c00278

                Chemistry
                Chemistry

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