Ruthenium-Catalyzed Electrochemical Dehydrogenative Alkyne Annulation DOI Creative Commons
Fan Xu, Yanjie Li, Chong Huang

и другие.

ACS Catalysis, Год журнала: 2018, Номер 8(5), С. 3820 - 3824

Опубликована: Март 9, 2018

A ruthenium-catalyzed electrochemical dehydrogenative annulation reaction of aniline derivatives and alkynes has been developed for the synthesis indoles. Electric current is used to recycle active ruthenium-based catalyst promote H2 evolution. The electrolysis operationally convenient as it employs a simple undivided cell, proceeds efficiently in an aqueous solution, insensitive air.

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

1966

Electrochemical strategies for C–H functionalization and C–N bond formation DOI Creative Commons
Markus D. Kärkäs

Chemical Society Reviews, Год журнала: 2018, Номер 47(15), С. 5786 - 5865

Опубликована: Янв. 1, 2018

This review provides an overview of the use electrochemistry as appealing platform for expediting carbon–hydrogen functionalization and carbon–nitrogen bond formation.

Язык: Английский

Процитировано

880

Bidentate Directing Groups: An Efficient Tool in C–H Bond Functionalization Chemistry for the Expedient Construction of C–C Bonds DOI
Supriya Rej, Yusuke Ano, Naoto Chatani

и другие.

Chemical Reviews, Год журнала: 2020, Номер 120(3), С. 1788 - 1887

Опубликована: Янв. 6, 2020

During the past decades, synthetic organic chemistry discovered that directing group assisted C–H activation is a key tool for expedient and siteselective construction of C–C bonds. Among various strategies, bidentate groups are now recognized as one most efficient devices selective functionalization certain positions due to fact its metal center permits fine, tunable, reversible coordination. The family permit types assistance be achieved, such N,N-dentate, N,O-dentate, N,S-dentate auxiliaries, which categorized based on coordination site. In this review, we broadly discuss bond reactions formation bonds with aid groups.

Язык: Английский

Процитировано

812

Electrochemical Arylation Reaction DOI Creative Commons
Siegfried R. Waldvogel,

Sebastian Lips,

Maximilian Selt

и другие.

Chemical Reviews, Год журнала: 2018, Номер 118(14), С. 6706 - 6765

Опубликована: Июль 2, 2018

Arylated products are found in various fields of chemistry and represent essential entities for many applications. Therefore, the formation this structural feature represents a central issue contemporary organic synthesis. By action electricity necessity leaving groups, metal catalysts, stoichiometric oxidizers, or reducing agents can be omitted part even completely. The replacement conventional reagents by sustainable not only will environmentally benign but also allows significant short cuts electrochemical In addition, methodology considered as inherently safe. current survey is organized cathodic anodic conversions well number groups being involved. some electroconversions used regenerated at electrode, whereas other electrotransformations free radical sequences exploited to afford highly process. aryl-substrate bond discussed aromatic substrates, heterocycles, multiple systems, saturated carbon substrates. This covers most seminal work advances past two decades area.

Язык: Английский

Процитировано

735

Recent Advances in Oxidative R1-H/R2-H Cross-Coupling with Hydrogen Evolution via Photo-/Electrochemistry DOI
Huamin Wang, Xinlong Gao,

Zongchao Lv

и другие.

Chemical Reviews, Год журнала: 2019, Номер 119(12), С. 6769 - 6787

Опубликована: Май 10, 2019

Photo-/electrochemical catalyzed oxidative R1-H/R2-H cross-coupling with hydrogen evolution has become an increasingly important issue for molecular synthesis. The dream of construction C-C/C-X bonds from readily available C-H/X-H release H2 can be facilely achieved without external chemical oxidants, providing a greener model bond formation. Given the great influence these reactions in organic chemistry, we give summary state art via photo/electrochemistry, and hope this review will stimulate development synthetic strategy near future.

Язык: Английский

Процитировано

649

Electrocatalytic C–H Activation DOI

Nicolas Sauermann,

Tjark H. Meyer, Youai Qiu

и другие.

ACS Catalysis, Год журнала: 2018, Номер 8(8), С. 7086 - 7103

Опубликована: Июнь 18, 2018

C–H activation has emerged as a transformative tool in molecular synthesis, but until recently oxidative activations have largely involved the use of stoichiometric amounts expensive and toxic metal oxidants, compromising overall sustainable nature chemistry. In sharp contrast, electrochemical been identified more efficient strategy that exploits storable electricity place byproduct-generating chemical reagents. Thus, transition-metal catalysts were shown to enable versatile reactions manner. While palladium catalysis set stage for C(sp2)–H C(sp3)–H functionalizations by N-containing directing groups, rhodium ruthenium allowed weakly coordinating amides acids. contrast these precious 4d transition metals, recent year witnessed emergence cobalt oxygenations, nitrogenations, C–C-forming [4+2] alkyne annulations. Thereby, silver(I) oxidants was prevented, improving environmentally benign catalysis. Herein, we summarize major advances organometallic otherwise inert bonds electrocatalysis through May 2018.

Язык: Английский

Процитировано

603

Organic Electrochemistry: Molecular Syntheses with Potential DOI Creative Commons
Cuiju Zhu, Nate W. J. Ang, Tjark H. Meyer

и другие.

ACS Central Science, Год журнала: 2021, Номер 7(3), С. 415 - 431

Опубликована: Март 9, 2021

Efficient and selective molecular syntheses are paramount to

Язык: Английский

Процитировано

582

Late-stage C–H functionalization offers new opportunities in drug discovery DOI
Lucas Guillemard, Nikolaos Kaplaneris, Lutz Ackermann

и другие.

Nature Reviews Chemistry, Год журнала: 2021, Номер 5(8), С. 522 - 545

Опубликована: Июль 13, 2021

Язык: Английский

Процитировано

582

C–H Activation: Toward Sustainability and Applications DOI Creative Commons
Toryn Dalton,

Teresa Faber,

Frank Glorius

и другие.

ACS Central Science, Год журнала: 2021, Номер 7(2), С. 245 - 261

Опубликована: Фев. 2, 2021

Since the definition of "12 Principles Green Chemistry" more than 20 years ago, chemists have become increasingly mindful need to conserve natural resources and protect environment through judicious choice synthetic routes materials. The direct activation functionalization C–H bonds, bypassing intermediate functional group installation is, in abstracto, step atom economic, but numerous factors still hinder sustainability large-scale applications. In this Outlook, we highlight research areas seeking overcome challenges activation: pursuit abundant metal catalysts, avoidance static directing groups, replacement oxidants, introduction bioderived solvents. We close by examining progress made subfield aryl borylation from its origins, highly efficient precious Ir-based systems, emerging 3d catalysts. future growth field will depend on industrial uptake, thus urge researchers strive toward sustainable activation.

Язык: Английский

Процитировано

575

Recent Advances in C–H Functionalization Using Electrochemical Transition Metal Catalysis DOI
Cong Ma, Ping Fang, Tian‐Sheng Mei

и другие.

ACS Catalysis, Год журнала: 2018, Номер 8(8), С. 7179 - 7189

Опубликована: Июнь 19, 2018

Electrochemical transition metal catalysis is a powerful strategy for organic synthesis because it obviates the use of stoichiometric chemical oxidants and reductants. C–H bond functionalization offers variety useful conversions simple ubiquitous molecules into diverse functional groups in single synthetic operation. This review summarizes recent progress merging electrochemistry with metal-catalyzed functionalization, specifically C–C, C–X (halogen), C–O, C–P, C–N formation.

Язык: Английский

Процитировано

524