Recent Progress in Situ Application of H2O2 Produced via Catalytic Synthesis DOI
Shuxin Zhang, Debin Zeng, Hui Wang

et al.

Chemistry - A European Journal, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 5, 2024

Abstract Industrial production of H 2 O requires lots energy and causes environmental pollution. Moreover, in subsequent applications, much economic loss could be produced during the transportation process its dilution process. Therefore, it is highly desirable for situ application . In recent years, catalytic synthesis , e. g., direct synthesis, electrocatalytic photocatalytic has attracted more attention because continuous low‐concentration by can directly used oxidation organic compounds, effectively avoiding shortcomings current industrial route. Here, we briefly reviewed latest processes via various routes. On this basis, summarized discussed typical conversion reactions, including ammoximation ketones, alcohols, C−H bonds, olefins. Some coupling reactions have shown excellent performance with high selectivity, cost been significantly reduced. Finally, utilization were analyzed, some strategies promoting efficiency proposed.

Language: Английский

Organocatalyzed Asymmetric Conjugate Addition of Alcohols to β‐Fluoroalkyl Vinylsulfones by Bifunctional Phosphonium Salt Catalyst DOI

Xingjie Luo,

Zhiyu Jiang,

Siqun Yang

et al.

Chemistry - A European Journal, Journal Year: 2024, Volume and Issue: 30(38)

Published: May 3, 2024

Chiral secondary alcohols, serving as essential structural motifs, hold significant potential for diverse applications. The exploration of effective synthetic strategies toward these compounds is both attractive and challenging. Herein, we present an asymmetric oxa-Michael reaction involving aliphatic alcohols nucleophiles β-fluoroalkyl vinylsulfones catalyzed by bifunctional phosphonium salt (BPS), achieving high yields excellent enantioselectivities (up to 98 % yield ee). Additionally, a sequential process including debenzylation, facilitated BPS/Lewis acid cooperation, was revealed synthesizing chiral alcohol in (81-88 %) with consistent stereoselectivities. Furthermore, mechanistic explorations subsequent results unveiled that the enantioselectivity originates from hydrogen-bonding ion-pair interactions between BPS catalyst substrates.

Language: Английский

Citations

0

Iodonium Salt‐Mediated Oxidation of Sulfides to Sulfoxides by DMSO DOI Creative Commons
Eleni Avramidou,

Agapi K. Triandafyllou,

Stavroula A. Zisopoulou

et al.

European Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: unknown

Published: Aug. 21, 2024

Abstract Compounds bearing the sulfoxide moiety display an important class of molecules in pharmaceutical industry. Many efforts have been made towards development novel, sustainable, easy‐to‐execute and industrially friendly processes. A novel iodonium‐salt‐mediated oxidation protocol for conversion sulfides into corresponding sulfoxides is reported, employing DMSO as oxidant. Several decorated with various functional groups were tested, leading to products good excellent yields remarkable chemoselectivity. The was successfully applied synthesis active ingredients (APIs) Sulforaphane Modafinil.

Language: Английский

Citations

0

Visible light-induced aerobic oxidation of an alkene catalyzed by thiobenzoic acid in water DOI
Wenjing Li, Chunye Liu, Lingling Liang

et al.

Organic Chemistry Frontiers, Journal Year: 2024, Volume and Issue: 11(19), P. 5429 - 5436

Published: Jan. 1, 2024

A metal-free, visible-light-catalyzed oxidative cleavage of the CC bond an alkene by thiobenzoic acid in water under O 2 atmosphere has been developed.

Language: Английский

Citations

0

The Oxidation of Electron-Rich Arenes Using a H2O2–Proline System DOI Creative Commons
Lloyd C. Chetty, Hendrik G. Kruger, Per I. Arvidsson

et al.

ACS Omega, Journal Year: 2024, Volume and Issue: 9(35), P. 37155 - 37162

Published: Aug. 22, 2024

This study introduces a novel proline-catalyzed oxidation system employing hydrogen peroxide to synthesize quinones from diverse range of substrates, including hydroquinones, phenols, resorcinols, aldehydes, and polycyclic aromatics. approach is well-aligned with green chemistry principles, offering more environmentally benign than earlier studies. Notably, this uses cost-effective reagents, proline as readily available organocatalyst, reduced equivalents H

Language: Английский

Citations

0

Visible photons for the regioselective nucleophilic ring opening of epoxides DOI Creative Commons

Beatrice Bernardoni,

Lorenzo Di Terlizzi,

Eirini M. Galathri

et al.

Green Chemistry, Journal Year: 2024, Volume and Issue: 26(18), P. 9833 - 9839

Published: Jan. 1, 2024

Herein, we introduce a visible-light promoted green, metal-free method for the regioselective nucleophilic ring opening of epoxides by exploiting arylazo sulfones as PhotoAcid Generators (PAGs).

Language: Английский

Citations

0

Maleic anhydride derivatives as catalysts for N-oxidation of pyridine using hydrogen peroxide DOI Creative Commons
Ghellyn Gajeles, Kyung‐Koo Lee, Sang Hee Lee

et al.

RSC Advances, Journal Year: 2024, Volume and Issue: 14(43), P. 31657 - 31662

Published: Jan. 1, 2024

The anhydride–diacid equilibrium is crucial for the catalytic cycle of maleic anhydride derivatives in N -oxidation pyridine with H 2 O . This system can replace stoichiometric peracids, such as m -CPBA, oxidants.

Language: Английский

Citations

0

Recent Progress in Situ Application of H2O2 Produced via Catalytic Synthesis DOI
Shuxin Zhang, Debin Zeng, Hui Wang

et al.

Chemistry - A European Journal, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 5, 2024

Abstract Industrial production of H 2 O requires lots energy and causes environmental pollution. Moreover, in subsequent applications, much economic loss could be produced during the transportation process its dilution process. Therefore, it is highly desirable for situ application . In recent years, catalytic synthesis , e. g., direct synthesis, electrocatalytic photocatalytic has attracted more attention because continuous low‐concentration by can directly used oxidation organic compounds, effectively avoiding shortcomings current industrial route. Here, we briefly reviewed latest processes via various routes. On this basis, summarized discussed typical conversion reactions, including ammoximation ketones, alcohols, C−H bonds, olefins. Some coupling reactions have shown excellent performance with high selectivity, cost been significantly reduced. Finally, utilization were analyzed, some strategies promoting efficiency proposed.

Language: Английский

Citations

0