Traditional and sustainable approaches for the construction of C–C bonds by harnessing C–H arylation DOI Creative Commons
Jagrit Grover, Gaurav Prakash, Nupur Goswami

и другие.

Nature Communications, Год журнала: 2022, Номер 13(1)

Опубликована: Фев. 28, 2022

Abstract Biaryl scaffolds are found in natural products and drug molecules exhibit a wide range of biological activities. In past decade, the transition metal-catalyzed C–H arylation reaction came out as an effective tool for construction biaryl motifs. However, traditional reactions have limitations like harsh conditions, narrow substrate scope, use additives etc. therefore encouraged synthetic chemists to look alternate greener approaches. This review aims draw general overview on bond formation C–C bonds with aid different methodologies, majorly highlighting sustainable

Язык: Английский

3d Transition Metals for C–H Activation DOI
Parthasarathy Gandeepan, Thomas Müller, Daniel Zell

и другие.

Chemical Reviews, Год журнала: 2018, Номер 119(4), С. 2192 - 2452

Опубликована: Ноя. 27, 2018

C–H activation has surfaced as an increasingly powerful tool for molecular sciences, with notable applications to material crop protection, drug discovery, and pharmaceutical industries, among others. Despite major advances, the vast majority of these functionalizations required precious 4d or 5d transition metal catalysts. Given cost-effective sustainable nature earth-abundant first row metals, development less toxic, inexpensive 3d catalysts gained considerable recent momentum a significantly more environmentally-benign economically-attractive alternative. Herein, we provide comprehensive overview on until summer 2018.

Язык: Английский

Процитировано

1980

Metallaphotoredox: The Merger of Photoredox and Transition Metal Catalysis DOI
Amy Chan, Ian B. Perry, Noah B. Bissonnette

и другие.

Chemical Reviews, Год журнала: 2021, Номер 122(2), С. 1485 - 1542

Опубликована: Ноя. 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.

Язык: Английский

Процитировано

1186

Photoredox-Catalyzed C–H Functionalization Reactions DOI

Natalie Holmberg‐Douglas,

David A. Nicewicz

Chemical Reviews, Год журнала: 2021, Номер 122(2), С. 1925 - 2016

Опубликована: Сен. 29, 2021

The fields of C–H functionalization and photoredox catalysis have garnered enormous interest utility in the past several decades. Many different scientific disciplines relied on strategies including natural product synthesis, drug discovery, radiolabeling, bioconjugation, materials, fine chemical synthesis. In this Review, we highlight use reactions. We separate review into inorganic/organometallic catalysts organic-based catalytic systems. Further subdivision by reaction class─either sp2 or sp3 functionalization─lends perspective tactical for these methods synthetic applications.

Язык: Английский

Процитировано

661

The Persistent Radical Effect in Organic Synthesis DOI
Dirk Leifert, Armido Studer

Angewandte Chemie International Edition, Год журнала: 2019, Номер 59(1), С. 74 - 108

Опубликована: Май 22, 2019

Abstract Radical–radical couplings are mostly nearly diffusion‐controlled processes. Therefore, the selective cross‐coupling of two different radicals is challenging and not a synthetically valuable transformation. However, if have lifetimes they generated at equal rates, will become dominant process. This high cross‐selectivity based on kinetic phenomenon called persistent radical effect (PRE). In this Review, an explanation PRE supported by simulations simple model systems provided. Radical stabilities discussed within context their lifetimes, various examples PRE‐mediated radical–radical in synthesis summarized. It shown that restricted to coupling with transient radical. If one partner longer‐lived than other radical, operates achieved. important point expands scope chemistry. The Review divided into parts, namely 1) or organic 2) “radical–metal crossover reactions”; here, metal‐centered species more generally transition‐metal complexes able react discussed—a field has flourished recently.

Язык: Английский

Процитировано

652

Alkyl Carbon–Carbon Bond Formation by Nickel/Photoredox Cross‐Coupling DOI
John A. Milligan, James P. Phelan, Shorouk O. Badir

и другие.

Angewandte Chemie International Edition, Год журнала: 2018, Номер 58(19), С. 6152 - 6163

Опубликована: Окт. 6, 2018

The union of photoredox and nickel catalysis has resulted in a renaissance radical chemistry as well the use nickel-catalyzed transformations, specifically for carbon-carbon bond formation. Collectively, these advances address longstanding challenge late-stage cross-coupling functionalized alkyl fragments. Empowered by notion that photocatalytically generated radicals readily undergo capture Ni complexes, wholly new feedstocks have been realized. Herein, we highlight recent developments several types cross-couplings are accessible exclusively through this approach.

Язык: Английский

Процитировано

568

The Evolution of High-Throughput Experimentation in Pharmaceutical Development and Perspectives on the Future DOI Creative Commons
Steven M. Mennen, Carolina Alhambra,

C. Liana Allen

и другие.

Organic Process Research & Development, Год журнала: 2019, Номер 23(6), С. 1213 - 1242

Опубликована: Май 7, 2019

High-throughput experimentation (HTE) has revolutionized the pharmaceutical industry, most notably allowing for rapid screening of compound libraries against therapeutic targets. The past decade also witnessed extension HTE principles toward realm small-molecule process chemistry. Today, major companies have created dedicated groups within their development teams, invested in automation technology to accelerate screening, or both. industry's commitment accelerating led innovations space. This review will deliver an overview latest best practices currently taking place our teams chemistry by sharing frequently studied transformations, perspective next several years field, and manual automated tools enable experimentation. A series case studies are presented exemplify state-of-the-art workflows developed laboratories.

Язык: Английский

Процитировано

450

Photons or Electrons? A Critical Comparison of Electrochemistry and Photoredox Catalysis for Organic Synthesis DOI
Nicholas E. S. Tay, Dan Lehnherr, Tomislav Rovis

и другие.

Chemical Reviews, Год журнала: 2021, Номер 122(2), С. 2487 - 2649

Опубликована: Ноя. 9, 2021

Redox processes are at the heart of synthetic methods that rely on either electrochemistry or photoredox catalysis, but how do and catalysis compare? Both approaches provide access to high energy intermediates (e.g., radicals) enable bond formations not constrained by rules ionic 2 electron (e) mechanisms. Instead, they 1e mechanisms capable bypassing electronic steric limitations protecting group requirements, thus enabling chemists disconnect molecules in new different ways. However, while providing similar intermediates, differ several physical chemistry principles. Understanding those differences can be key designing transformations forging disconnections. This review aims highlight these similarities between comparing their underlying principles describing impact electrochemical photochemical methods.

Язык: Английский

Процитировано

364

Recent advances in visible light-activated radical coupling reactions triggered by (i) ruthenium, (ii) iridium and (iii) organic photoredox agents DOI Creative Commons
Jonathan D. Bell, John A. Murphy

Chemical Society Reviews, Год журнала: 2021, Номер 50(17), С. 9540 - 9685

Опубликована: Янв. 1, 2021

Visible light-activated reactions continue to expand and diversify. The example shown here is a Birch reduction achieved by organophotoredox reagents.

Язык: Английский

Процитировано

347

Photocatalytic Late-Stage C–H Functionalization DOI
Peter Bellotti, Huan‐Ming Huang,

Teresa Faber

и другие.

Chemical Reviews, Год журнала: 2023, Номер 123(8), С. 4237 - 4352

Опубликована: Янв. 24, 2023

The emergence of modern photocatalysis, characterized by mildness and selectivity, has significantly spurred innovative late-stage C–H functionalization approaches that make use low energy photons as a controllable source. Compared to traditional strategies, photocatalysis paves the way toward complementary and/or previously unattainable regio- chemoselectivities. Merging compelling benefits with workflow offers potentially unmatched arsenal tackle drug development campaigns beyond. This Review highlights photocatalytic strategies small-molecule drugs, agrochemicals, natural products, classified according targeted bond newly formed one. Emphasis is devoted identifying, describing, comparing main mechanistic scenarios. draws critical comparison between established ionic chemistry photocatalyzed radical-based manifolds. aims establish current state-of-the-art illustrate key unsolved challenges be addressed in future. authors aim introduce general readership functionalization, specialist practitioners evaluation methodologies, potential for improvement, future uncharted directions.

Язык: Английский

Процитировано

336

Photoinduced intermolecular hydrogen atom transfer reactions in organic synthesis DOI Creative Commons
Hui Cao, Xinxin Tang,

Haidi Tang

и другие.

Chem Catalysis, Год журнала: 2021, Номер 1(3), С. 523 - 598

Опубликована: Май 24, 2021

Язык: Английский

Процитировано

333