Advances in Selective Oxidation of Organic Sulfides by Hydrogen Peroxide over Titanium Catalyst DOI
Lucjan Chmielarz

Chemistry & Chemical Technology, Год журнала: 2025, Номер 19(1), С. 34 - 51

Опубликована: Март 25, 2025

Hydrogen peroxide (H2O2) is a versatile oxidant used in various chemical syntheses, including the selective oxidation of organic compounds and conversion pollutants wastewater. The increasing interest H2O2 as “green oxidant” largely due to environmental considerations assigned clean nature hydrogen an because its by-product only water. selected catalytic processes sulfide oxidation, method for production valuable chemicals, well potential crude oil desulfurization are presented discussed. Special attention paid Ti-based systems these processes.

Язык: Английский

A sustainable photochemical aerobic sulfide oxidation: access to sulforaphane and modafinil DOI Creative Commons

Elpida Skolia,

Petros L. Gkizis, Christoforos G. Kokotos

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2022, Номер 20(29), С. 5836 - 5844

Опубликована: Янв. 1, 2022

Photochemical aerobic synthesis of sulfoxides from sulfides, utilizing air as the oxidant, 2-Me-THF green solvent and LED 370 nm. 427 nm, CFL or sunlight irradiation source. Application in sulforaphane modafinil.

Язык: Английский

Процитировано

24

Cyrene: a bio-based solvent for the Mizoroki–Heck reaction of aryl iodides DOI Creative Commons
Naya A. Stini, Petros L. Gkizis, Christoforos G. Kokotos

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2022, Номер 21(2), С. 351 - 358

Опубликована: Ноя. 30, 2022

Cyrene is employed as the reaction medium in Mizoroki–Heck cross-coupling between aryl iodides with acrylates, acrylamides or styrene. Its application synthesis of piperlotine A demonstrated.

Язык: Английский

Процитировано

24

Photochemical [2 + 2] Cycloaddition of Alkenes with Maleimides: Highlighting the Differences between N-Alkyl vs N-Aryl Maleimides DOI Creative Commons

Elpida Skolia,

Christoforos G. Kokotos

ACS Organic & Inorganic Au, Год журнала: 2022, Номер 3(2), С. 96 - 103

Опубликована: Дек. 8, 2022

Throughout the last 15 years, there has been increased research interest in use of light promoting organic transformations. [2 + 2] Cycloadditions are usually performed photochemically; however, literature precedent on reaction between olefins and maleimides is limited to a handful examples, focusing mainly N-aliphatic or using metal catalysts for visible-light driven reactions N-aromatic maleimides. Herein, we identify differences reactivity N-alkyl N-aryl For our optimized protocols, case maleimides, with alkenes proceeds under 370 nm irradiation absence an external photocatalyst, leading products high yields. In requires thioxanthone as photosensitizer 440 irradiation.

Язык: Английский

Процитировано

23

An Efficient Light‐Mediated Protocol for the Direct Amide Bond Formation via a Novel Carboxylic Acid Photoactivation Mode by Pyridine‐CBr4 DOI Creative Commons
Olga G. Mountanea,

Danai Psathopoulou,

Christiana Mantzourani

и другие.

Chemistry - A European Journal, Год журнала: 2023, Номер 29(35)

Опубликована: Апрель 4, 2023

The direct amide bond formation between a carboxylic acid and an amine still constitutes challenging reaction for both academia industry. We demonstrate herein that several pairs of amines (halogen acceptors) organohalogen sources may be used the photochemical amidation under either UVA or sunlight irradiation. Our studies led to identification pyridine-CBr4 as efficient agent perform synthesis LED 370 nm irradiation, avoiding super-stoichiometric quantities. An extended substrate scope was demonstrated, showing widely amino carboxyl protecting groups are compatible with this protocol, while number industrially interesting products bioactive compounds were synthesized. Direct infusion-high resolution mass spectrometry suggest unprecedented type activation mode upon involving generation symmetric anhydride, active ester pyridine N-oxide mixed anhydride hypobromous acid.

Язык: Английский

Процитировано

13

A Photochemical Protocol for the Synthesis of Weinreb and Morpholine Amides from Carboxylic Acids DOI Creative Commons

Asimina Bourboula,

Olga G. Mountanea,

George Krasakis

и другие.

European Journal of Organic Chemistry, Год журнала: 2023, Номер 26(24)

Опубликована: Фев. 27, 2023

Abstract In recent years, the development of light‐mediated methods for synthetic applications has attracted high interest, because such constitute alternative approaches production valuable chemical products. We study herein a photochemical protocol synthesis Weinreb amides and morpholine from carboxylic acids. Various acids were directly coupled to N , O ‐dimethylhydroxylamine, upon irradiation with either LED 370 nm or sunlight in presence 4‐dimethylaminopyridine bromotrichloromethane, providing moderate yields. Similarly, obtained satisfactory yields under irradiation. Thus, versatile building blocks may be efficiently synthesized by approaches, without need coupling reagents pre‐activation

Язык: Английский

Процитировано

11

Oxidation of N-trifluoromethylthio sulfoximines using NaOCl·5H2O DOI Creative Commons
Žan Testen, Marjan Jereb

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(10), С. 2012 - 2020

Опубликована: Янв. 1, 2024

N -Trifluoromethylthio sulfoximines were oxidized using NaOCl·5H 2 O to the corresponding novel -trifluoromethylsulfaneylidene in high yields and with excellent green metrics.

Язык: Английский

Процитировано

4

Expanding the Use of Benzothioxanthene Imides to Photochemistry: Eco‐Friendly Aerobic Oxidation of Sulfides to Sulfoxides DOI Creative Commons

Stamatis K. Serviou,

Petros L. Gkizis, Darío Puchán Sánchez

и другие.

ChemSusChem, Год журнала: 2024, Номер unknown

Опубликована: Июнь 13, 2024

The sulfoxide moiety is one of the most commonly utilized groups in pharmaceutical and industrial chemistry. need for sustainability easy accessibility to moieties deemed necessary, due its ubiquity natural products potentially pharmaceutically active compounds. In this context, we report herein a sustainable, aerobic environmentally friendly photochemical protocol based on use benzothioxathene imide as photocatalyst selectively oxidize sulfides under mild irradiation (456 nm), very low catalyst loading (0.01 mol %) water. addition, demonstrate compatibility our with wide scope substrates, latter was successfully applied synthesis biologically-active Sulforaphane Modafinil.

Язык: Английский

Процитировано

4

Unveiling the Synthetic Potential of Conjugated Organic Molecule as Efficient Photo-catalytic Trifluoromethylation and Photo-cocatalytic C–N Coupling Reaction DOI

Yumin Pan,

Tingting Xie,

Jiming Peng

и другие.

Catalysis Letters, Год журнала: 2025, Номер 155(2)

Опубликована: Янв. 3, 2025

Язык: Английский

Процитировано

0

A mild and scalable one-pot synthesis of N-substituted 2-aminobenzimidazoles via visible light mediated cyclodesulfurization DOI Creative Commons

Tanawat Rerkrachaneekorn,

Rose Malina Annuur, Soraya Pornsuwan

и другие.

Scientific Reports, Год журнала: 2025, Номер 15(1)

Опубликована: Фев. 3, 2025

Abstract A visible light mediated photocatalyst-free synthesis of N -substituted 2-aminobenzimidazoles directly from o -phenylenediamines and isothiocyanates is developed in a one-pot fashion. This reaction proceeds through three steps: -substitution -phenylenediamines, thiourea formation cyclodesulfurization. method enables the rapid efficient structurally diverse 2-aminobenzimidazoles, achieving yields up to 92% across 69 examples. The practicality demonstrated by gram-scale synthesis. key advantages this include use less toxic solvent aqueous media, elimination photocatalyst, simple, practical setup (one-pot, open-flask, ambient temperature). Mechanistic insights are gathered control experiments, including on/off cycles radical inhibition studies. results indicate that involves with pathway light.

Язык: Английский

Процитировано

0

Response Surface Method (RSM) Process Optimization of Sulfides Oxidation in the Presence of Orange Peel Extract Immobilized Magnetic Hybrid Nanocomposite Catalyst DOI Open Access
Taiebeh Tamoradi, Amanollah Zarei Ahmady, Bikash Karmakar

и другие.

Applied Organometallic Chemistry, Год журнала: 2025, Номер 39(3)

Опубликована: Фев. 5, 2025

ABSTRACT The oxidative transformation of sulfides to sulfoxides over magnetic green catalysts is one the most important applications in pharmaceuticals. In this report, we demonstrate step‐by‐step fabrication and synthesis CoFe 2 O 4 , CuFe Fe 3 nanocomposite modified with orange peel extract complexes as advanced high‐performance materials. One goals project was use phenolic acid phytochemicals catalytic process. newly synthesized nanocomposites were characterized by several analytical methods. Utilizing Box–Behnken experimental design response surface methodology (RSM), reaction parameters such amount catalyst, hydrogen peroxide, duration improved. Furthermore, without experiencing a discernible loss reactivity sulfide oxidation reaction, effortlessly magnetically retrieved may be employed repeatedly.

Язык: Английский

Процитировано

0