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-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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Transition Metal-Catalyzed Organic Reactions under Visible Light: Recent Developments and Future Perspectives

ACS Catalysis, Journal Year: 2020, Volume and Issue: 10(16), P. 9170 - 9196

Published: July 20, 2020

The development of transition metal (TM) catalysis for organic synthesis under visible light without recourse to typical photoredox catalysts has become a rapidly growing area research and been actively explored in the past several years. Distinct from extensively developed catalysis, which photocatalyst generally does not directly participate bond-forming process, photocatalyst/TM synergistic absorbs photon energy transfers TM catalyst through redox or transfer this Review focuses on summarizing recent developments photocatalytic reactions that use complexes both absorb catalytic bond formation involving covalently bonded intermediate. contents are categorized by used (Pd, Cu, Co, Ni, Mn, Au, Rh, Fe, Ru), with descending sequence according number examples reported each metal, provide an overview April 2020. Future perspectives personal opinions regarding expanding field also discussed.

Language: Английский

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Single Electron Transfer-Induced Redox Processes Involving N-(Acyloxy)phthalimides

ACS Catalysis, Journal Year: 2021, Volume and Issue: 11(3), P. 1640 - 1683

Published: Jan. 20, 2021

The past decade has witnessed the emergence of N-(acyloxy)phthalimides (NHPI esters) and its derivatives at forefront synthetic methods facilitating construction diverse molecular frameworks from readily available carboxylic acid feedstock. NHPI esters are predisposed to undergo reductive fragmentation via a single electron transfer (SET) process under thermal, photochemical, or electrochemical conditions generate corresponding carbon- nitrogen-centered radicals that participate in multitude transformations forge carbon–carbon carbon–heteroatom bonds. chemistry involving received broad applicability not only well-designed cascade annulations but also medicinal natural product synthesis. This comprehensive Review, broadly categorized according nature bond formation, details progress made this field since initial discovery by providing representative examples with mechanistic details, an emphasis on challenges future directions.

Language: Английский

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Transition metal-catalysed allylic functionalization reactions involving radicals

Chemical Society Reviews, Journal Year: 2020, Volume and Issue: 49(17), P. 6186 - 6197

Published: Jan. 1, 2020

In this tutorial review, different types of transition metal-catalysed allylic functionalization reactions involving radicals are highlighted.

Language: Английский

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Three-Component, Interrupted Radical Heck/Allylic Substitution Cascade Involving Unactivated Alkyl Bromides

Journal of the American Chemical Society, Journal Year: 2020, Volume and Issue: 142(22), P. 10173 - 10183

Published: May 7, 2020

Developing efficient and selective strategies to approach complex architectures containing (multi)stereogenic centers has been a long-standing synthetic challenge in both academia industry. Catalytic cascade reactions represent powerful means of rapidly leveraging molecular complexity from simple feedstocks. Unfortunately, carrying out Heck-type involving unactivated (tertiary) alkyl halides remains an unmet owing unavoidable β-hydride elimination. Herein, we show that modular, practical, general palladium-catalyzed, radical three-component coupling can indeed overcome the aforementioned limitations through interrupted Heck/allylic substitution sequence mediated by visible light. Selective 1,4-difunctionalization 1,3-dienes, such as butadiene, achieved employing different commercially available nitrogen-, oxygen-, sulfur-, or carbon-based nucleophiles bromides (>130 examples, mostly >95:5 E/Z, >20:1 rr). Sequential C(sp3)–C(sp3) C–X (N, O, S) bonds have constructed efficiently with broad scope high functional group tolerance. The flexibility versatility strategy illustrated gram-scale reaction streamlined syntheses ether, sulfone, tertiary amine products, some which would be difficult access via currently established methods.

Language: Английский

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Bifunctional reagents in organic synthesis

Nature Reviews Chemistry, Journal Year: 2021, Volume and Issue: 5(5), P. 301 - 321

Published: April 12, 2021

Language: Английский

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Photoinduced Palladium-Catalyzed Carbofunctionalization of Conjugated Dienes Proceeding via Radical-Polar Crossover Scenario: 1,2-Aminoalkylation and Beyond

Journal of the American Chemical Society, Journal Year: 2020, Volume and Issue: 142(22), P. 9932 - 9937

Published: May 14, 2020

A photoinduced palladium-catalyzed 1,2-carbofunctionalization of conjugated dienes has been developed. This mild modular approach, which does not require employment exogeneous photosensitizers and external oxidants, allows for efficient highly regio- stereoselective synthesis a broad range allylic amines from readily available 1,3-dienes, alkyl iodides, amines. Employment O- C-nucleophiles toward oxyalkylation dialkylation products was also demonstrated. putative π-allyl palladium radical-polar crossover path is proposed as key event in this three-component coupling process. The utility protocol highlighted by its application derivatization several amine-containing drugs.

Language: Английский

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Photoinduced Copper-Catalyzed Asymmetric C–O Cross-Coupling

Journal of the American Chemical Society, Journal Year: 2021, Volume and Issue: 143(33), P. 13382 - 13392

Published: Aug. 10, 2021

The construction of carbon–heteroatom bonds is one the most active areas research in organic chemistry because function molecules often derived from presence heteroatoms. Although considerable advances have recently been achieved radical-involved catalytic asymmetric C–N bond formation, there has little progress corresponding C–O bond-forming processes. Here, we describe a photoinduced copper-catalyzed cross-coupling readily available oxime esters and 1,3-dienes to generate diversely substituted allylic with high regio- enantioselectivity (>75 examples; up 95% ee). reaction proceeds at room temperature under excitation by purple light-emitting diodes (LEDs) features use single, earth-abundant copper-based chiral catalyst as both photoredox for radical generation source induction coupling. Combined experimental density functional theory (DFT) computational studies suggest formation π-allylcopper complexes redox-active bifunctional reagents through radical–polar crossover process.

Language: Английский

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Visible‐Light‐Induced 1,3‐Aminopyridylation of [1.1.1]Propellane with N‐Aminopyridinium Salts

Angewandte Chemie International Edition, Journal Year: 2021, Volume and Issue: 60(14), P. 7873 - 7879

Published: Jan. 7, 2021

Through the formation of an electron donor-acceptor (EDA) complex, strain-release aminopyridylation [1.1.1]propellane with N-aminopyridinium salts as bifunctional reagents enabled direct installation amino and pyridyl groups onto bicyclo[1.1.1]pentane (BCP) frameworks in absence external photocatalyst. The robustness this method to synthesize 1,3-aminopyridylated BCPs under mild metal-free conditions is highlighted by late-stage modification structurally complex biorelevant molecules. Moreover, strategy was extended P-centered CF3 radicals for unprecedented incorporation such functional pyridine across BCP core a three-component coupling. This practical lays foundation straightforward construction new valuable C4-pyridine-functionalized chemical entities, thus significantly expanding range accessibility BCP-type bioisosteres applications drug discovery.

Language: Английский

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