Electrochemical promoted three-component reaction to unsymmetric thiosulfonates DOI
Hong-Min Lin,

Sai-Yan Ren,

Fei‐Hu Cui

et al.

Chemical Communications, Journal Year: 2024, Volume and Issue: 60(75), P. 10394 - 10397

Published: Jan. 1, 2024

Compounds comprising S-S bonds serve as significant pharmacological scaffolds in medicinal chemistry and natural products. We have devised an efficient electrochemical method for the construction of asymmetric disulfide bonds, leading to synthesis unsymmetric thiosulfonates. Compared with existing methods, our work not only avoids use metals oxidants, but also realizes operation a one-pot three-component method, which makes this strategy extremely attractive.

Language: Английский

Biomass-derived carbon applications in the field of supercapacitors: Progress and prospects DOI
Wenjie Lu,

Youxin Si,

Chongrui Zhao

et al.

Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: 495, P. 153311 - 153311

Published: June 21, 2024

Language: Английский

Citations

46

Recent advances in organic electrosynthesis using heterogeneous catalysts modified electrodes DOI
Li Ma,

Xianang Gao,

Xin Liu

et al.

Chinese Chemical Letters, Journal Year: 2022, Volume and Issue: 34(4), P. 107735 - 107735

Published: Aug. 10, 2022

Language: Английский

Citations

35

The Synthesis of α-Keto Acetals from Terminal Alkynes and Alcohols via Synergistic Interaction of Organoselenium Catalysis and Electrochemical Oxidation DOI

Ding Ding,

Liang Xu, Yu Wei

et al.

The Journal of Organic Chemistry, Journal Year: 2022, Volume and Issue: 87(7), P. 4912 - 4917

Published: Feb. 18, 2022

Herein, an unprecedented electrochemical approach for the synthesis of α-keto acetals has been established from readily available terminal alkynes and alcohols. By merging organoselenium-catalyzed processes, desired products are obtained at room temperature in absence basic or metallic additives, with carbonyl acetal motifs incorporated simultaneously across triple bonds a single operation.

Language: Английский

Citations

28

Regioselective Synthesis of N2-Aryl 1,2,3-Triazoles via Electro-oxidative Coupling of Enamines and Aryldiazonium Salts DOI
Mrinmay Baidya,

Samrat Mallick,

Suman De Sarkar

et al.

Organic Letters, Journal Year: 2022, Volume and Issue: 24(6), P. 1274 - 1279

Published: Feb. 3, 2022

An efficient synthetic route for the construction of N2-aryl 1,2,3-triazoles is reported via sequential C-N bond formation and electro-oxidative N-N coupling under metal-free conditions. Readily accessible 2-aminoacrylates aryldiazonium salts were used as starting materials, developed protocol displays excellent functional group tolerance, allowing an extensive range substrate scope up to 91% isolated yield. Various mechanistic studies, along with isolation intermediate adduct, refer successive ionic radical reaction sequences.

Language: Английский

Citations

25

Electrochemical Generation of Nitrogen‐centered Radicals and its Application for the Green Synthesis of Heterocycles DOI Creative Commons

Kseniia Titenkova,

Daniil A. Chaplygin,

Леонид Л. Ферштат

et al.

ChemElectroChem, Journal Year: 2024, Volume and Issue: 11(17)

Published: Aug. 12, 2024

Abstract Electrochemistry became a unique and powerful tool for the preparation of plethora valuable chemical species including functional materials, drug candidates clinically approved pharmaceuticals. Organic electrosynthesis well satisfies main goals green chemistry development is considered as one useful approaches toward creation sustainable future. Since nitrogen heterocyclic scaffolds still retain their importance construction novel materials medications, emerging trends in organic electrochemistry discovery synthetic methods assembly subunits. In this regard, provides an efficient platform environmentally benign generation various nitrogen‐centered radicals which are prominent intermediates synthesis heterocycles. Review, recent developments heterocycles via electrochemical summarized. The special emphasis devoted to influence solvent, electrodes electrolytes on step, since these crucial parameters regulate process efficiency.

Language: Английский

Citations

6

Cross-dehydrogenative N–N couplings DOI Creative Commons
Alexis Tabey,

Pooja Y. Vemuri,

Frédéric W. Patureau

et al.

Chemical Science, Journal Year: 2021, Volume and Issue: 12(43), P. 14343 - 14352

Published: Jan. 1, 2021

For more than a century, the dehydrogenative formation of N–N bonds has remained mostly confidential. Several cross-dehydrogenative coupling methods have appeared recently, promising soon to come broad applicability concept.

Language: Английский

Citations

25

Decoupled Photoelectrochemical Cerium-Catalyzed Oxydichlorination of Alkynes: Slow Releasing of Chloride Ions and Chlorine Radicals DOI

Dongxu Shao,

Yanwei Wu,

Shaochen Hu

et al.

ACS Sustainable Chemistry & Engineering, Journal Year: 2022, Volume and Issue: 10(31), P. 10294 - 10302

Published: July 27, 2022

Synthetic photoelectrochemistry shows significant advantages in handling of reactive intermediates via a sustainable way and has developed to be the frontier single electron transfer chemistry. The exploration new photoelectrocatalysts, especially uncommon metal-based ones, will contribute exploitation synthetic strategies. Benefiting from reversible redox ability photoactivity, cerium salt is expected become photo-electro-response medium generate active species. In this work, with green reaction system (neutral conditions renewable light electricity as energy sources), we novel type generation Cl· electrooxidation photoinduced ligand-to-metal charge by using CeCl3 photoelectrocatalyst oxydichlorination aryl acetylene. Importantly, found that slow releasing chloride ions chlorine radicals played an important role radical chlorination. addition, several analytical methods including cyclic voltammetry, X-ray photoelectron spectroscopy, paramagnetic resonance, control experiments were conducted investigate reasonable mechanism.

Language: Английский

Citations

17

Transition metal-free electrochemical fluorotrifluoromethylation of Styrenes DOI
Yi Lu, Zhirui Liu, Chao Liu

et al.

Organic Chemistry Frontiers, Journal Year: 2023, Volume and Issue: 10(5), P. 1283 - 1288

Published: Jan. 1, 2023

An environmentally friendly electrochemical fluorotrifluoromethylation of styrenes is developed using CF 3 SO 2 Na and Et N·3HF as the F-containing donor reagents. This synthetic strategy features step economy sustainability.

Language: Английский

Citations

10

The literature of heterocyclic chemistry, part XXII, 2022 DOI
Галина А. Газиева, Yu. B. Evdokimenkova, N. O. Soboleva

et al.

Advances in heterocyclic chemistry, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

Language: Английский

Citations

0

Synthesis of Unsymmetric Thiosulfonates Starting from N-Substituted O-Thiocarbamates: Easy Access to the S–SO2 Bond DOI

Cheng‐Li Yang,

Xue-Jie Gao,

Xin‐Yi Jiang

et al.

The Journal of Organic Chemistry, Journal Year: 2022, Volume and Issue: 87(17), P. 11656 - 11668

Published: Aug. 12, 2022

Using phenyliodine diacetate as an oxidant and nickel acetate a promoter, wide range of unsymmetric thiosulfonates could be furnished easily in moderate to excellent yields starting from N-substituted O-thiocarbamates sodium sulfinates. This protocol features mild conditions, short reaction times, high atomic utilization, which can provide alternative method for the synthesis thiosulfonates. In addition, scaled up on gram scale, showing potential application value industry.

Language: Английский

Citations

16