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

Ziying Liu,

Miao Liu

и другие.

Tetrahedron, Год журнала: 2024, Номер 162, С. 134130 - 134130

Опубликована: Авг. 1, 2024

Язык: Английский

Recent Advances on C—H Functionalization via Oxidative Electrophotocatalysis DOI

Aman Hasil,

Rui Chang,

Juntao Ye

и другие.

Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(3), С. 728 - 728

Опубликована: Янв. 1, 2024

Язык: Английский

Процитировано

8

Electrochemical synthesis and transformation of organoboron compounds DOI

Chunyu Yin,

Shuai Tang,

Jiatong Mei

и другие.

Organic Chemistry Frontiers, Год журнала: 2023, Номер 10(13), С. 3361 - 3377

Опубликована: Янв. 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.

Язык: Английский

Процитировано

11

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

и другие.

Chemical Synthesis, Год журнала: 2024, Номер 4(1)

Опубликована: Март 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.

Язык: Английский

Процитировано

3

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

ChemElectroChem, Год журнала: 2025, Номер unknown

Опубликована: Фев. 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.

Язык: Английский

Процитировано

0

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

и другие.

Chemical Reviews, Год журнала: 2025, Номер unknown

Опубликована: Март 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.

Язык: Английский

Процитировано

0

Metal‐Free Electrochemical Hydroboration of Olefins DOI

Qilin Yuan,

Xiǎo Zhang, Lin Guo

и другие.

Advanced Synthesis & Catalysis, Год журнала: 2023, Номер 365(11), С. 1788 - 1793

Опубликована: Май 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.

Язык: Английский

Процитировано

6

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

Ziying Liu,

Miao Liu

и другие.

Tetrahedron, Год журнала: 2024, Номер 162, С. 134130 - 134130

Опубликована: Авг. 1, 2024

Язык: Английский

Процитировано

0