Rapid metal-free reduction of aromatic nitro compounds to aromatic amines in MeOH/H2O with B2pin2 DOI
Wei Wang,

Ziying Liu,

Miao Liu

et al.

Tetrahedron, Journal Year: 2024, Volume and Issue: 162, P. 134130 - 134130

Published: Aug. 1, 2024

Language: Английский

Recent Advances on C—H Functionalization via Oxidative Electrophotocatalysis DOI

Aman Hasil,

Rui Chang,

Juntao Ye

et al.

Chinese Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 44(3), P. 728 - 728

Published: Jan. 1, 2024

Language: Английский

Citations

8

Iodoarene Activation: Take a Leap Forward toward Green and Sustainable Transformations DOI Creative Commons
Toshifumi Dohi, Elghareeb E. Elboray, Kotaro Kikushima

et al.

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

Published: March 7, 2025

Constructing chemical bonds under green sustainable conditions has drawn attention from environmental and economic perspectives. The dissociation of (hetero)aryl-halide is a crucial step most arylations affording (hetero)arene derivatives. Herein, we summarize the (hetero)aryl halides activation enabling direct (hetero)arylation trapping reagents construction highly functionalized (hetero)arenes benign conditions. strategies for aryl iodides are classified into (a) hypervalent iodoarene followed by functionalization thermal/photochemical conditions, (b) aryl-I bond in presence bases with/without organic catalysts promoters, (c) photoinduced presence/absence organophotocatalysts, (d) electrochemical direct/indirect electrolysis mediated organocatalysts mediators acting as electron shuttles, (e) electrophotochemical redox-active organocatalysts. These modes result exhibiting diverse reactivity formal cations/radicals/anions aryne precursors. coupling these reactive intermediates with leads to facile selective formation C-C C-heteroatom bonds. ecofriendly, inexpensive, functional group-tolerant offer alternatives transition metal-based catalysis.

Language: Английский

Citations

1

Electrochemical synthesis and transformation of organoboron compounds DOI

Chunyu Yin,

Shuai Tang,

Jiatong Mei

et al.

Organic Chemistry Frontiers, Journal Year: 2023, Volume and Issue: 10(13), P. 3361 - 3377

Published: Jan. 1, 2023

This review highlights the recent advances in both electrochemical borylation and hydroboration to synthesize organoboron compounds transformation of construct carbon–carbon carbon–heteroatom bonds.

Language: Английский

Citations

13

Electrochemical-induced hydrofunctionalizations of alkenes and alkynes DOI Open Access
Yahui Zhang, Xiangyu Zhao, Guangyan Qing

et al.

Chemical Synthesis, Journal Year: 2024, Volume and Issue: 4(1)

Published: March 1, 2024

The hydrofunctionalizations of readily available alkenes and alkynes are one the most effective useful routes to afford diverse value-added compounds. Although traditional hydrofunctionalization strategies catalyzed by metal catalysts present convenient approaches, they also accompanied resource consumption environmental crisis. Electrosynthesis, as a renewable sustainable technology, has become cost- atom-efficient synthetic route. In this review, electrochemical-induced summarized presented. each section, electrochemical strategy access hydrogenation other (hydroboration, hydrosilylation, hydroalkylation, hydroalkoxylation, hydrocyanation, hydrocarboxylation, etc. ) products elaborated in detail separately. Finally, current challenges prospects for unsaturated carbon‒carbon (C‒C) bonds discussed briefly.

Language: Английский

Citations

3

Electrochemical Borylation of C−C and C−Het Bonds DOI Creative Commons
T. Cheung, Hairong Lyu

ChemElectroChem, Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 19, 2025

Abstract Recently, electrochemical methods have been harnessed as a transition metal‐free strategy for borylation reactions in the synthesis of organoboron compounds. This article reviews C−C and C−Het bonds, offering systematic discussion C−C, C−N, C−O, C−S bond reactions. These transformations are applied to substrates including ammonium salts, aryl azo sulfones, carboxylic acids, arylhydrazines, nitroarenes, alcohols, thioethers, showcasing broad compatibility. Additionally, review discusses reaction mechanisms, scalability, practical applications these strategies. The concludes by outlining future research directions reactions, aiming at expending their incorporating boron into wider array organic compounds, challenging unactivated C−F borylations.

Language: Английский

Citations

0

Metal‐Free Electrochemical Hydroboration of Olefins DOI

Qilin Yuan,

Xiǎo Zhang, Lin Guo

et al.

Advanced Synthesis & Catalysis, Journal Year: 2023, Volume and Issue: 365(11), P. 1788 - 1793

Published: May 12, 2023

Abstract Herein, we reported the electrochemical hydroboration of olefins to access organoboron derivatives in a one‐pot reaction under air and at room temperature. This manifold was applied broad range alkenes with 40–90% yields good functional group tolerance without using metal catalyst or an additional hydride source. Mechanistic studies suggested that this anodic oxidation conducted undivided cell allowing production boron radical species, which initiates event by addition process.

Language: Английский

Citations

6

Rapid metal-free reduction of aromatic nitro compounds to aromatic amines in MeOH/H2O with B2pin2 DOI
Wei Wang,

Ziying Liu,

Miao Liu

et al.

Tetrahedron, Journal Year: 2024, Volume and Issue: 162, P. 134130 - 134130

Published: Aug. 1, 2024

Language: Английский

Citations

0