Metallaphotoredox: The Merger of Photoredox and Transition Metal Catalysis

Chemical Reviews, Journal Year: 2021, Volume and Issue: 122(2), P. 1485 - 1542

Published: Nov. 18, 2021

The merger of photoredox catalysis with transition metal catalysis, termed metallaphotoredox has become a mainstay in synthetic methodology over the past decade. Metallaphotoredox combined unparalleled capacity for bond formation broad utility photoinduced electron- and energy-transfer processes. Photocatalytic substrate activation allowed engagement simple starting materials metal-mediated bond-forming Moreover, electron or energy transfer directly key organometallic intermediates provided novel modes entirely complementary to traditional catalytic platforms. This Review details contextualizes advancements molecule construction brought forth by metallaphotocatalysis.

Language: Английский

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Visible Light-Driven Radical-Mediated C–C Bond Cleavage/Functionalization in Organic Synthesis

Chemical Reviews, Journal Year: 2020, Volume and Issue: 121(1), P. 506 - 561

Published: May 29, 2020

Thermal C–C bond cleavage reactions allow the construction of structurally diverse molecular skeletons via predictable and efficient reorganizations. Visible light photoredox-catalyzed radical-mediated have recently emerged as a powerful alternative method for overcoming thermodynamic kinetic barrier in scaffolds. In recent years, plethora elegant useful been invented, products are sometimes otherwise inaccessible by classic thermal reactions. Considering great influence synthetic potential these reactions, we provide summary state art visible light-driven cleavage/functionalization strategies with specific emphasis on working models. We hoped that this review will be medicinal organic chemists inspire further reaction development interesting area.

Language: Английский

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Copper’s rapid ascent in visible-light photoredox catalysis

Science, Journal Year: 2019, Volume and Issue: 364(6439)

Published: May 2, 2019

Visible-light photoredox catalysis offers a distinct activation mode complementary to thermal transition metal catalyzed reactions. The vast majority of processes capitalizes on precious ruthenium(II) or iridium(III) complexes that serve as single-electron reductants oxidants in their photoexcited states. As low-cost alternative, organic dyes are also frequently used but general suffer from lower photostability. Copper-based photocatalysts rapidly emerging, offering not only economic and ecological advantages otherwise inaccessible inner-sphere mechanisms, which have been successfully applied challenging transformations. Moreover, the combination conventional with copper(I) copper(II) salts has emerged an efficient dual catalytic system for cross-coupling

Language: Английский

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Visible Light-Induced Transition Metal Catalysis

Chemical Reviews, Journal Year: 2021, Volume and Issue: 122(2), P. 1543 - 1625

Published: Oct. 8, 2021

In recent years, visible light-induced transition metal catalysis has emerged as a new paradigm in organic photocatalysis, which led to the discovery of unprecedented transformations well improvement known reactions. this subfield complex serves double duty by harvesting photon energy and then enabling bond forming/breaking events mostly via single catalytic cycle, thus contrasting established dual photocatalysis an exogenous photosensitizer is employed. addition, approach often synergistically combines catalyst–substrate interaction with photoinduced process, feature that uncommon conventional photoredox chemistry. This Review describes early development advances emerging field.

Language: Английский

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When Light Meets Nitrogen-Centered Radicals: From Reagents to Catalysts

Accounts of Chemical Research, Journal Year: 2020, Volume and Issue: 53(5), P. 1066 - 1083

Published: April 14, 2020

ConspectusNitrogen-centered radicals (NCRs) are a versatile class of highly reactive species that have longer history than the classical carbon-based in synthetic chemistry. Depending on N-hybridization and substitution patterns, NCRs can serve as electrophiles or nucleophiles to undergo various radical transformations. Despite their power, progress nitrogen-radical chemistry is still slow compared with popularity carbon radicals, considerable potential has been largely underexplored, which is, concluded by Zard, mainly hampered "a dearth convenient access these lack awareness pertaining reactivity".Over past decade, visible-light photoredox catalysis established powerful toolbox chemists use generate diverse range intermediates from native organic functional groups via single electron transfer process energy under mild reaction conditions. This catalytic strategy typically obviates need for external stoichiometric activation reagents toxic initiators often enables traditionally inaccessible ionic chemical reactions. On basis our long-standing interest nitrogen catalysis, we emphasized tactic discover develop novel methods generating controlled fashion applications. In this Account, describe recent advances development visible-light-driven photoredox-catalyzed generation applications.Inspired natural biological proton-coupled (PCET) process, first developed oxidative deprotonation activate N–H bonds hydrazones, benzamides, sulfonamides give corresponding With species, then achieved 5-exo 6-endo cyclizations well cascade reactions regioselective manner, providing variety potentially useful heterocycles. To further expand repertoire possible NCRs, also revealed iminyl derived O-acyl cycloalkanone oxime esters, facile ring-opening C–C bond cleavage cyanoalkyl radicals. These newly formed bond-forming allow synthesis distally functionalized alkyl nitriles. Stimulated studies, wide copper-catalyzed cross-coupling Because inherent transient properties, heteroatom-centered underexplored synthesis. Building understanding fundamental time concept NCR covalent involves situ-photogenerated allyl sulfones, vinylcyclopropanes, N-tosyl vinylaziridines. thus enabled efficient difunctionalization alkenes late-stage modification complex biologically active molecules.In panoramic picture contributions since 2014 application systems field studies provide not only functionally rich molecules but some insight into exploration new reactivity modes NCRs.

Language: Английский

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Visible light photocatalysis in the late-stage functionalization of pharmaceutically relevant compounds

Chemical Society Reviews, Journal Year: 2020, Volume and Issue: 50(2), P. 766 - 897

Published: Dec. 22, 2020

Recent developments and future prospects of visible-light photocatalysis in the late-stage functionalization pharmaceuticals natural bioactive compounds.

Language: Английский

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The emerging roles of N6-methyladenosine (m6A) deregulation in liver carcinogenesis

Molecular Cancer, Journal Year: 2020, Volume and Issue: 19(1)

Published: Feb. 28, 2020

Abstract Liver cancer is a common worldwide. Although the etiological factors of liver carcinogenesis are well defined, underlying molecular mechanisms remain largely elusive. Epigenetic deregulations, such as aberrant DNA methylation and histone modifications, play critical role in carcinogenesis. Analogous to core proteins, reversible chemical modifications on mRNA have recently been recognized important regulatory control gene expression. N6-methyladenosine (m6A) most prevalent internal modification mammalian cells. m6A for controlling many cellular biological processes. Deregulation has implicated human carcinogenesis, including cancer. In this review, we summarize recent findings regulation its impacts normal We will focus deregulation regulators diseases cancers. highlight clinical relevance also discuss potential exploiting diagnosis therapeutics.

Language: Английский

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Strategies to Generate Nitrogen-centered Radicals That May Rely on Photoredox Catalysis: Development in Reaction Methodology and Applications in Organic Synthesis

Chemical Reviews, Journal Year: 2021, Volume and Issue: 122(2), P. 2353 - 2428

Published: Oct. 8, 2021

For more than 70 years, nitrogen-centered radicals have been recognized as potent synthetic intermediates. This review is a survey designed for use by chemists engaged in target-oriented synthesis. summarizes the recent paradigm shift access to and application of N-centered enabled visible-light photocatalysis. broadens streamlines approaches many small molecules because photocatalysis conditions are mild. Explicit attention paid innovative advances N–X bonds radical precursors, where X = Cl, N, S, O, H. clarity, key mechanistic data noted, available. Synthetic applications limitations summarized illuminate tremendous utility photocatalytically generated radicals.

Language: Английский

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Cleavage of Carbon–Carbon σ-Bonds of Four-Membered Rings

Chemical Reviews, Journal Year: 2020, Volume and Issue: 121(1), P. 264 - 299

Published: Sept. 23, 2020

This article reviews synthetic transformations involving cleavage of a carbon-carbon bond four-membered ring, with particular focus on the examples reported during period from 2011 to end 2019. Most significant is progress catalytic reactions oxidative addition bonds onto transition metals or β-carbon elimination metal alkoxides. When they are looked at perspectives, offer unique and efficient methods build complex natural products structures that difficult construct by conventional methods. On other hand, β-scission radical intermediates has also attracted increasing attention as an alternative elementary step cleave bonds. Its site-selectivity often complementary metal-catalyzed reactions. In addition, Lewis acid-mediated thermally induced ring-opening cyclobutanone derivatives garnered renewed attention. whole, these demonstrate potentials structurally strained ring compounds for construction organic skeletons.

Language: Английский

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Catalytic cascade reactions by radical relay

Chemical Society Reviews, Journal Year: 2019, Volume and Issue: 48(17), P. 4626 - 4638

Published: Jan. 1, 2019

Radical cascade reactions are an attractive tool for the rapid construction of complex molecular architectures. Although a large number powerful radical cascades have been developed, stoichiometric amounts reagents and/or additives often required to mediate these processes. relay strategies, in which character is recycled, require only catalytic amount reagent and particularly as they promise that high atom economy. This tutorial review highlights recent advances this rapidly developing area by setting out dissecting reaction designs underpinning state-of-the-art processes involving relays. Advances field will open door more efficient synthesis with far-reaching benefits makers end-users molecules.

Language: Английский

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