Enantioselective Radical Reactions Using Chiral Catalysts

Chemical Reviews, Journal Year: 2022, Volume and Issue: 122(6), P. 5842 - 5976

Published: Jan. 24, 2022

Benefiting from the impressive increase in fundamental knowledge, last 20 years have shown a continuous burst of new ideas and consequently plethora catalytic methods for enantioselective radical reactions. This review aims to provide complete survey progress achieved over this latter period. The first part focuses on use chiral organocatalysts, these include catalysts covalently linked substrate those that interact with by weaker interactions like hydrogen bonds. second is devoted transition-metal redox catalysis which organized according increasing atomic number first-row transition metals (Ti, Cr, Fe, Mn, Co, Ni, Cu). Bioinspired manganese- iron-mediated hydroxylations oxidations are also discussed. A specific section dedicated reactivity Ru, Rh, Ir complexes as Lewis acids special focus at metal. Absorption photons result different events such energy transfer, single-electron hydrogen-atom transfer facilitating formation radicals. Organocatalysis has been successfully combined photocatalysts, opened pathways enlarging precursors available. merger photocatalysis organo- or metalla-photocatalysis brought novelty allowed discovery large original transformations. enzyme-catalyzed reactions involving intermediates largely benefit visible-light irradiation included review. provides comprehensive inventory goal detailing reaction mechanisms involved transformations any nonspecialist could find their own creativity invent yet unknown applications.

Language: Английский

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Visible-Light-Driven Catalytic Reductive Carboxylation with CO₂

ACS Catalysis, Journal Year: 2020, Volume and Issue: 10(19), P. 10871 - 10885

Published: Aug. 28, 2020

Carbon dioxide (CO2) is an important C1 source for the generation of carboxylic acids and derivatives. Stoichiometric catalytic carboxylation nucleophiles, including organometallic reagents, with CO2 has been widely investigated. Since many kinds reagents are prepared from electrophiles, transition-metal-catalyzed direct diverse electrophiles attracted much attention high step economy user-friendly protocols. Although significant progress achieved, use stoichiometric metallic or pyrophoric reductants common. The renaissance photochemistry seen numerous efforts devoted to light-driven CO2, which become one most active directions in this field. In Perspective, we summarize recent advances visible-light-driven reductive substrates, such as unsaturated hydrocarbons, organic (pseudo)halides, imines, presence mild electron donors, amines, Hantzsch esters, formates. We highlight mechanisms reactions, can proceed absence a photoredox catalyst dual visible light photoredox/transition metal system. also discuss future field offer some insight into challenges that remain.

Language: Английский

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Exploiting attractive non-covalent interactions for the enantioselective catalysis of reactions involving radical intermediates

Nature Chemistry, Journal Year: 2020, Volume and Issue: 12(11), P. 990 - 1004

Published: Oct. 19, 2020

Language: Английский

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Recent advances in tandem selenocyclization and tellurocyclization with alkenes and alkynes

Organic Chemistry Frontiers, Journal Year: 2020, Volume and Issue: 7(19), P. 3100 - 3119

Published: Jan. 1, 2020

This review highlights recent progress in tandem selenocyclization and tellurocyclization with alkenes alkynes, an emphasis on the scopes, limitations mechanisms of these different reactions.

Language: Английский

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Access to axially chiral styrenes via a photoinduced asymmetric radical reaction involving a sulfur dioxide insertion

Chem Catalysis, Journal Year: 2022, Volume and Issue: 2(1), P. 164 - 177

Published: Jan. 1, 2022

Language: Английский

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Catalytic Asymmetric Synthesis of Atropisomers Bearing Multiple Chiral Elements: An Emerging Field

Angewandte Chemie International Edition, Journal Year: 2023, Volume and Issue: 63(3)

Published: Nov. 2, 2023

With the rapid development of asymmetric catalysis, demand for enantioselective synthesis complex and diverse molecules with different chiral elements is increasing. Owing to unique features atropisomerism, catalytic atropisomers has attracted a considerable interest from chemical science community. In particular, introducing additional elements, such as carbon centered chirality, heteroatomic planar helical into provides an opportunity incorporate new properties axially compounds, thus expanding potential applications atropisomers. Thus, it important perform transformations synthesize bearing multiple elements. spite challenges in transformations, recent years, chemists have devised powerful strategies under organocatalysis or metal synthesizing wide range enantioenriched Therefore, become emerging field. This review summarizes progress this field indicates challenges, thereby promoting horizon.

Language: Английский

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Enantioselective [2π + 2σ] Cycloadditions of Bicyclo[1.1.0]butanes with Vinylazaarenes through Asymmetric Photoredox Catalysis

Journal of the American Chemical Society, Journal Year: 2024, Volume and Issue: 146(12), P. 8372 - 8380

Published: March 18, 2024

Here we present a highly enantioselective [2π + 2σ] photocycloaddition of bicyclo[1.1.0]butanes (BCBs). The reaction uses variety vinylazaarenes as partners and is catalyzed by polycyclic aromatic hydrocarbon (PAH)-containing chiral phosphoric acid bifunctional photosensitizer. A wide array pharmaceutically important bicyclo[2.1.1]hexane (BCH) derivatives have been synthesized with high yields, enantioselectivity, diastereoselectivity. In addition to the diverse 1-ketocarbonyl-3-substituted BCBs, α/β-substituted are compatible such an unprecedented photoredox catalytic pathway, resulting in successful assembly all-carbon quaternary stereocenter or two adjacent tertiary stereocenters on product.

Language: Английский

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Asymmetric photoredox catalytic formal de Mayo reaction enabled by sensitization-initiated electron transfer

Nature Chemistry, Journal Year: 2024, Volume and Issue: 16(7), P. 1169 - 1176

Published: April 2, 2024

Language: Английский

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Catalytic asymmetric photocycloaddition reactions mediated by enantioselective radical approaches

Chemical Society Reviews, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

The use of olefins in the construction cyclic compounds represents a powerful strategy for advancing pharmaceutical industry.

Language: Английский

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Catalytic Reductive Cross Coupling and Enantioselective Protonation of Olefins to Construct Remote Stereocenters for Azaarenes

Journal of the American Chemical Society, Journal Year: 2021, Volume and Issue: 143(10), P. 4024 - 4031

Published: March 2, 2021

A novel enantioselective protonation protocol that is triggered by reductive cross coupling of olefins reported. When under cooperative photoredox and chiral hydrogen-bonding catalytic conditions using a terminal reductant, various α-branched vinylketones with diverse vinylazaarenes could provide important enantioenriched azaarene derivatives containing tertiary stereocenters at their remote δ-position high yields enantioselectivities. This reaction system also suitable for vinylazaarenes, thus successfully assembling elusive 1,4-stereocenters. The convenient late-stage modifications products, especially the formation ε-tertiary ε-heteroquaternary carbon stereocenters, further highlight synthetic value this method. Control experiments density functional theory (DFT) calculations were conducted to elucidate plausible mechanism origins regioselectivity stereoselectivity.

Language: Английский

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