A Review of Electrochemical Synthesis and Transformations of Small Organic Molecules: Sulfoximines, Isoxazolines, and Benzimidazoles DOI
Sanjay M. Madurkar, Girdhar Pal Singh, Siddharth Sharma

et al.

Current Green Chemistry, Journal Year: 2024, Volume and Issue: 12(2), P. 85 - 116

Published: Sept. 26, 2024

In the realm of synthetic organic chemistry, environmentally friendly manipulation small molecules has gained prominence. One particularly promising approach is electrochemical synthesis, which offers a green and sustainable alternative to using hazardous toxic redox reagents. By harnessing electric current from renewable sources like sunlight or wind, synthesis emerges as viable replacement for conventional methods. This review article provides comprehensive exploration method, delving into its background applications in synthesizing transforming various molecules, including sulfoximines, isoxazolines, benzimidazoles, more. aims shed light on potential greener more way conducting transformations.

Language: Английский

Electrochemical oxidative cross coupling of NH-sulfoximines with disulfides DOI
Shuai Zhang, Meiqian Hu, Changsheng Qin

et al.

New Journal of Chemistry, Journal Year: 2024, Volume and Issue: 48(6), P. 2576 - 2583

Published: Jan. 1, 2024

An electrochemical method for thioetherification of NH-sulfoximines with disulfides is reported. The utilization electrochemistry facilitating these reactions eliminates the necessity external oxidants, bases, and metal catalysts.

Language: Английский

Citations

11
Electrochemical N-Acylation of Sulfoximine with Hydroxamic Acid DOI
Wenxiu Huang, Shoucai Wang, Mingzhe Li

et al.

The Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: 88(24), P. 17511 - 17520

Published: Nov. 29, 2023

Despite the widespread applications of sulfoximines, green and efficient access to functionalized sulfoximines remains a challenge. By employing an electrochemical strategy, we describe approach for construction N-aroylsulfoximines, which features broad substrate scope, mild reaction conditions, safety on gram scale, no need external oxidant transition metal catalysts.

Language: Английский

Citations

6
Electrochemical Oxidative Thioetherification of Aldehyde Hydrazones with Thiophenols DOI
Meiqian Hu, Xiaolin Yang, Shuai Zhang

et al.

Organic & Biomolecular Chemistry, Journal Year: 2024, Volume and Issue: 22(29), P. 5907 - 5912

Published: Jan. 1, 2024

An electrochemically promoted oxidative dehydrogenation cross-coupling reaction between aldehyde hydrazones and thiophenols is demonstrated for the first time, which results in a variety of thioetherified products moderate to excellent yields.

Language: Английский

Citations

0
Direct N H heteroarylation of NH-sulfoximines under electrochemical conditions DOI
Changsheng Qin, Jingfang Wang,

Fang Gao

et al.

Molecular Catalysis, Journal Year: 2024, Volume and Issue: 568, P. 114485 - 114485

Published: Aug. 27, 2024

Language: Английский

Citations

0
Electrochemical Selenocyclization of N-Alkyl anilines: Access to 3-Selenyl quinolines DOI

Longqiang Zhao,

Huimin Li,

Mengyu Peng

et al.

Tetrahedron, Journal Year: 2024, Volume and Issue: unknown, P. 134257 - 134257

Published: Sept. 1, 2024

Language: Английский

Citations

0
A Review of Electrochemical Synthesis and Transformations of Small Organic Molecules: Sulfoximines, Isoxazolines, and Benzimidazoles DOI
Sanjay M. Madurkar, Girdhar Pal Singh, Siddharth Sharma

et al.

Current Green Chemistry, Journal Year: 2024, Volume and Issue: 12(2), P. 85 - 116

Published: Sept. 26, 2024

In the realm of synthetic organic chemistry, environmentally friendly manipulation small molecules has gained prominence. One particularly promising approach is electrochemical synthesis, which offers a green and sustainable alternative to using hazardous toxic redox reagents. By harnessing electric current from renewable sources like sunlight or wind, synthesis emerges as viable replacement for conventional methods. This review article provides comprehensive exploration method, delving into its background applications in synthesizing transforming various molecules, including sulfoximines, isoxazolines, benzimidazoles, more. aims shed light on potential greener more way conducting transformations.

Language: Английский

Citations

0