Polymer up-cycling by mangana-electrocatalytic C(sp3)–H azidation without directing groups DOI Creative Commons
Isaac Maksso, Ramesh C. Samanta, Yifei Zhan

et al.

Chemical Science, Journal Year: 2023, Volume and Issue: 14(30), P. 8109 - 8118

Published: Jan. 1, 2023

The chemical up-cycling of polymers into value-added materials offers a unique opportunity to place plastic waste in new value chain towards circular economy. Herein, we report the selective polystyrenes and polyolefins C(sp3)-H azidated under electrocatalytic conditions. functionalized were obtained with high retention mass average molecular functionalization through chemo-selective mangana-electrocatalysis. Our strategy proved be broadly applicable variety homo- copolymers. Polyethylene, polypropylene as well post-consumer polystyrene by this approach, thereby avoiding use hypervalent-iodine reagents stoichiometric quantities means electrocatalysis. This study, hence, represents oxidant-free polymer electro-oxidation. electrocatalysis scalable, which highlights its feature for green hydrogen economy evolution reaction (HER).

Language: Английский

Electrocatalysis as an enabling technology for organic synthesis DOI
Luiz F. T. Novaes, Jinjian Liu, Yifan Shen

et al.

Chemical Society Reviews, Journal Year: 2021, Volume and Issue: 50(14), P. 7941 - 8002

Published: Jan. 1, 2021

Electrochemistry has recently gained increased attention as a versatile strategy for achieving challenging transformations at the forefront of synthetic organic chemistry. Electrochemistry's unique ability to generate highly reactive radical and ion intermediates in controlled fashion under mild conditions inspired development number new electrochemical methodologies preparation valuable chemical motifs. Particularly, recent developments electrosynthesis have featured an use redox-active electrocatalysts further enhance control over selective formation downstream reactivity these intermediates. Furthermore, electrocatalytic mediators enable proceed manner that is mechanistically distinct from purely methods, allowing subversion kinetic thermodynamic obstacles encountered conventional synthesis. This review highlights key innovations within past decade area electrocatalysis, with emphasis on mechanisms catalyst design principles underpinning advancements. A host oxidative reductive are discussed grouped according classification transformation nature electrocatalyst.

Language: Английский

Citations

872

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

Teresa Faber,

Frank Glorius

et al.

ACS Central Science, Journal Year: 2021, Volume and Issue: 7(2), P. 245 - 261

Published: Feb. 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.

Language: Английский

Citations

575

Recent advances in organic electrosynthesis employing transition metal complexes as electrocatalysts DOI
Cong Ma, Ping Fang,

Zhao‐Ran Liu

et al.

Science Bulletin, Journal Year: 2021, Volume and Issue: 66(23), P. 2412 - 2429

Published: July 13, 2021

Language: Английский

Citations

293

Radical C(sp3)–H functionalization and cross-coupling reactions DOI
Dung L. Golden, Sung‐Eun Suh, Shannon S. Stahl

et al.

Nature Reviews Chemistry, Journal Year: 2022, Volume and Issue: 6(6), P. 405 - 427

Published: May 17, 2022

Language: Английский

Citations

192

Electrochemical generation of nitrogen-centered radicals for organic synthesis DOI Creative Commons
Na Chen, Hai‐Chao Xu

Green Synthesis and Catalysis, Journal Year: 2021, Volume and Issue: 2(2), P. 165 - 178

Published: March 29, 2021

There is a resurgence of interests in organic electrochemistry, which generally accepted as green synthetic tool. In this context, many electrochemical methods have been developed the past decade to access various nitrogen-centered radicals (NCRs) from readily available precursors controlled fashion, enabling rapid development NCR-mediated new reactions for construction nitrogen-containing compounds. review, recent advances chemistry electrochemically generated NCRs are critically highlighted, based on strategies their formation and types NCRs. Focus put mechanism generation different applications.

Language: Английский

Citations

161

Electrochemical Late-Stage Functionalization DOI Creative Commons
Yulei Wang, Suman Dana, Hao Long

et al.

Chemical Reviews, Journal Year: 2023, Volume and Issue: 123(19), P. 11269 - 11335

Published: Sept. 26, 2023

Late-stage functionalization (LSF) constitutes a powerful strategy for the assembly or diversification of novel molecular entities with improved physicochemical biological activities. LSF can thus greatly accelerate development medicinally relevant compounds, crop protecting agents, and functional materials. Electrochemical synthesis has emerged as an environmentally friendly platform transformation organic compounds. Over past decade, electrochemical late-stage (eLSF) gained major momentum, which is summarized herein up to February 2023.

Language: Английский

Citations

141

New Strategies for the Synthesis of Aliphatic Azides DOI
Paramasivam Sivaguru, Yongquan Ning, Xihe Bi

et al.

Chemical Reviews, Journal Year: 2021, Volume and Issue: 121(7), P. 4253 - 4307

Published: Feb. 26, 2021

Aliphatic azides are a versatile class of compounds found in variety biologically active pharmaceuticals. These also recognized as useful precursors for the synthesis range nitrogen-based scaffolds therapeutic drugs, compounds, and functional materials. In light growing importance aliphatic both chemical biological sciences, vast array synthetic strategies preparation structurally diverse have been developed over past decades. However, to date, this topic has not subject dedicated review. This review aims provide concise overview modern access that emerged since 2010. The discussed azidation reactions include (a) C–C multiple bonds, (b) C–H (c) direct transformation vinyl into other azides, (d) miscellaneous azides. We critically discuss outcomes generality uniqueness different mechanistic rationale each selected reactions. challenges potential opportunities outlined.

Language: Английский

Citations

117

Exploring Electrochemical C(sp3)–H Oxidation for the Late-Stage Methylation of Complex Molecules DOI
Luiz F. T. Novaes,

Justin S. K. Ho,

Kaining Mao

et al.

Journal of the American Chemical Society, Journal Year: 2022, Volume and Issue: 144(3), P. 1187 - 1197

Published: Jan. 11, 2022

The "magic methyl" effect, a dramatic boost in the potency of biologically active compounds from incorporation single methyl group, provides simple yet powerful strategy employed by medicinal chemists drug discovery process. Despite significant advances, methodologies that enable selective C(sp3)–H methylation structurally complex agents remain very limited. In this work, we disclose modular, efficient, and for α-methylation protected amines (i.e., amides, carbamates, sulfonamides) means electrochemical oxidation. Mechanistic analysis guided our development an improved protocol on basis classic Shono oxidation reaction, which features broad reaction scope, high functional group compatibility, operational simplicity. Importantly, system is amenable to late-stage functionalization targets containing basic nitrogen groups are prevalent medicinally agents. When combined with organozinc-mediated C–C bond formation, enabled direct myriad amine derivatives including those have previously been explored effect. This synthesis thus circumvents multistep de novo currently necessary access such has potential accelerate efforts.

Language: Английский

Citations

114

Electronic control over site-selectivity in hydrogen atom transfer (HAT) based C(sp3)–H functionalization promoted by electrophilic reagents DOI
Marco Galeotti, Michela Salamone, Massimo Bietti

et al.

Chemical Society Reviews, Journal Year: 2022, Volume and Issue: 51(6), P. 2171 - 2223

Published: Jan. 1, 2022

Leveraging on electronic effects in both the substrate and HAT reagent, site-selectivity can be implemented C(sp 3 )–H bond functionalization.

Language: Английский

Citations

99

The interplay of polar effects in controlling the selectivity of radical reactions DOI
Alessandro Ruffoni, Rory C. Mykura, Massimo Bietti

et al.

Nature Synthesis, Journal Year: 2022, Volume and Issue: 1(9), P. 682 - 695

Published: Aug. 1, 2022

Language: Английский

Citations

97