Advances in Cross and Oxidative Coupling Reactions of NH-Sulfoximines – A review DOI

Hala Adam Elzubier Adam,

Sihan Zhou, Qingle Zeng

et al.

Chemical Communications, Journal Year: 2024, Volume and Issue: unknown

Published: Dec. 23, 2024

Due to the special structure and physicochemical properties of sulfoximines, research on sulfoximines has achieved great progress in recent decades, especially chemical medicinal fields. This review highlights advancements N-functionalization NH-sulfoximines, focusing classical cross-coupling reactions with electrophilic agents oxidative coupling extensive organic compounds, including specific (hetero)arenes, alkenes (1,4-naphthoquinones), alkanes (cyclohexanes), nucleophiles (thiols, disulfides, sulfinates, diarylphosphine oxides), organyl boronic acids, arylhydrazines. Transition metal-catalyzed, metal-free, electrochemical radical are discussed. also reports discusses mechanistic pathways some typical reactions.

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

Continuous flow reactions in the preparation of active pharmaceutical ingredients and fine chemicals DOI
Guilherme M. Martins, Felipe C. Braga, Pedro P. de Castro

et al.

Chemical Communications, Journal Year: 2024, Volume and Issue: 60(24), P. 3226 - 3239

Published: Jan. 1, 2024

This feature article presents an overview of continuous flow chemistry, including photoflow and electroflow technologies in the preparation active pharmaceutical ingredients (APIs) fine chemical intermediates.

Language: Английский

Citations

10

Recent Advances in Electrochemical Sulfonylation using Sodium Sulfinates as Sulfonyl Radical Precursors DOI
Sen Liang,

Jia‐Xin Gu,

Cheng‐Chu Zeng

et al.

Current Organic Chemistry, Journal Year: 2024, Volume and Issue: 28(2), P. 105 - 116

Published: Jan. 1, 2024

Abstract: Sodium sulfinates have been widely utilized as sulfonyl radical precursors for preparing a diverse array of value-added sulfur-containing compounds (sulfones, sulfonamides, sulfonates, thiosulfonates, etc.) through S-C, S-N, S-O and S-S bonds formation reactions. Organic electrosynthesis has become an attractive alternative to conventional methods redox reactions because it utilizes electric current instead chemical agents. As such, the electrochemical generation radicals from sodium their applications in organic attracted much attention. In this review, recent advances sulfonylation involving since 2015 were reviewed, along with related reaction mechanisms.

Language: Английский

Citations

8

Solar-driven photoelectrochemical conversion of biomass: recent progress, mechanistic insights and potential scalability DOI

Caidi Jin,

Mingxia Han,

Yuheng Wu

et al.

Energy & Environmental Science, Journal Year: 2024, Volume and Issue: 17(20), P. 7459 - 7511

Published: Jan. 1, 2024

This review provides a comprehensive overview on the mechanism of photoelectrochemical biomass conversion and highlights extension dual-function cells for valorization paired with more valuable half-reactions.

Language: Английский

Citations

7

Chemo‐ and Regio‐selective Dual‐Functionalization of Arenes: Synthesis of Multi‐Functional Aromatics via Aromaticity Destruction‐Reconstruction Process DOI

Saddam Husen,

Ravindra Kumar

European Journal of Organic Chemistry, Journal Year: 2025, Volume and Issue: unknown

Published: April 3, 2025

Abstract Dual functionalizations of arenes promise to remain a powerful and versatile strategy for the synthesis complex molecules with diverse applications in various fields. Dearomatization‐Functionalization‐rearomatization emerges as tool chemo‐ regioselective functionalization via 2,5‐cyclohexadienone/2,5‐cyclohexadienimines, which can be easily accessible from phenols or anilines. 2,5‐Cyclohexadienones serve an “aromatic be” synthon multiple electrophilic centres, providing opportunity towards their functionalization. While mono‐functionalization was widely explored covered literature, simultaneous dual two distinct coupling partners offer rapid molecular diversification around aromatic rings. Diverse functional groups/coupling have been introduced regio‐selectively. The synthetic processes adopted are generally sustainable free transition metals exotic conditions. This review showcased advancement developing phenols/anilines site‐selective multi‐functional through aromaticity‐destruction‐functionalization‐construction strategy.

Language: Английский

Citations

0

Electrochemical synthesis: A green & powerful approach to modern organic synthesis and future directions DOI
Sadia Rani, Najoua Sbei, Seyfeddine Rahali

et al.

Chinese Chemical Letters, Journal Year: 2025, Volume and Issue: unknown, P. 111216 - 111216

Published: April 1, 2025

Language: Английский

Citations

0

Applications of Electrophotocatalysis in C‐H Functionalization of Organic Molecules. DOI
Samuel Andrejčák, Michal Májek

Chemistry - A European Journal, Journal Year: 2024, Volume and Issue: 30(57)

Published: July 6, 2024

Electrophotocatalysis (EPC) has evolved as a new scientific discipline around the boundary of highly active fields: electrochemistry and photocatalysis. EPC allows us to combine energy light electric potential activate previously inaccessible compounds via single-electron transfer (SET). Herein, we review most essential applications C-H functionalization molecules. This work discusses mechanisms that can be encountered when designing such processes analyzes technical aspects performing reactions in laboratory.

Language: Английский

Citations

2

Electrochemical C−H/C−C Bond Oxygenation: A Potential Technology for Plastic Depolymerization DOI Creative Commons
Sadia Rani, Samina Aslam, K. B. Lal

et al.

The Chemical Record, Journal Year: 2023, Volume and Issue: 24(3)

Published: Dec. 8, 2023

Herein, we provide eco-friendly and safely operated electrocatalytic methods for the selective oxidation directly or with water, air, light, metal catalyst other mediators serving as only oxygen supply. Heavy metals, stoichiometric chemical oxidants, harsh conditions were drawbacks of earlier oxidative cleavage techniques. It has recently come to light that a crucial stage in deconstruction plastic waste utilization biomass is activation inert C(sp

Language: Английский

Citations

4

Copper‐Promoted Oxidative Amide‐Assisted Radical Selenylation of Anilides and N‐Arylsulfonamides with Diselenides DOI
Lou Shi,

Penghui Xu,

Yingchun Ma

et al.

Asian Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 13(5)

Published: March 21, 2024

Abstract A direct selenylation of N ‐arylsulfonamides and anilides using environmentally friendly readily available copper promoted assisted by amide is presented. This method provided convenient access for various reactions, demonstrating a wide range substrates strong tolerance to functional groups. According the selection reaction substrates, products can be isolated obtain regioselectivity ortho ‐, para or unprecedented , ‐diselenylation products. Such transformation was elucidated proposed copper‐promoted amide‐assisted radical mechanism.

Language: Английский

Citations

1

Photoelectrochemical Approaches for the Functionalization of C-H Bonds DOI
Alexandra Jorea, Andrea Capucciati, Davide Ravelli

et al.

Elsevier eBooks, Journal Year: 2024, Volume and Issue: unknown

Published: Jan. 1, 2024

Language: Английский

Citations

0