Synthesis of diarylsulphide/diarylselenide embedded pyrazole-fused isocoumarins and isatin/ninhydrin hydrazones via acid catalyzed solvent and temperature controlled reactions DOI
Sayanwita Panja,

Arun Dhurey,

Animesh Pramanik

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 11, 2024

Room temperature stirring of a mixture chalcogenated arylhydrazones and ninhydrin in dichloromethane (DCM) the presence acid leads to formation pyrazole-fused isocoumarins, substituted with diarylsulphide/diarylselenide moiety. On other hand, refluxing same protic polar solvent ethanol produces containing hydrazones. Further study reveals that, like ninhydrin, isatin can also generate corresponding hydrazones at C-3 position under similar reaction conditions.

Язык: Английский

Visible-Light-Promoted α-C(sp3)–H Amidation of Cyclic Ethers under Redox-Neutral Conditions DOI
Shuangqing Li, Xiufang Xu, Jianhui Chen

и другие.

Organic Letters, Год журнала: 2025, Номер unknown

Опубликована: Март 16, 2025

Reported herein is a visible-light-promoted strategy for the α-C(sp3)–H amidation of cyclic ethers using N-acyloxyamide as an oxidative amidating reagent. This transformation provides straightforward approach to various α-amidated under metal- and additive-free conditions. The synthetic utility products was demonstrated through facile transformations, including reduction, allylation, acylation, sulfonamidation, gram-scale reactions. Preliminary mechanistic studies suggest radical/radical cross-coupling process, with C(sp3)–H bond cleavage identified rate-determining step.

Язык: Английский

Процитировано

1

Rose bengal photocatalyzed expeditious multicomponent synthesis of 3,4‐dihydropyrimidin‐2‐(1H)‐ones/thiones under visible light irradiation DOI

Divyani P. Patel,

Vishwa K. Patel,

Satish K. Singh

и другие.

Journal of Heterocyclic Chemistry, Год журнала: 2024, Номер 61(9), С. 1455 - 1461

Опубликована: Июль 10, 2024

Abstract The combination of visible light, a renewable and green energy source, rose bengal, non‐toxic organic dye as photoredox catalyst, is an easy efficient method for synthesizing 3,4‐dihydropyrimidin‐2(1 H )‐ones/thiones in EtOH at ambient temperature very short reaction time. present work offers simple operation, workup, rapid conversion, excellent product yields, while accommodating wide range substrates. Rose bengal‐based photocatalytic approach permits foremost sustainability, which delivers economic environmental rewards.

Язык: Английский

Процитировано

4

A carbazole-based fully conjugated sp2c D–A covalent organic polymer for visible light mediated photocatalytic degradation of rhodamine B and Rose Bengal DOI Creative Commons
Kamal Kant Verma, K. R. Justin Thomas

Materials Advances, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

We demonstrate that the sp 2 carbon-linked carbazole based covalent organic polymer is a potential photocatalyst for remediation of dyes such as rhodamine B and Rose Bengal.

Язык: Английский

Процитировано

0

Recent advances of 9-fluorenone in photoredox catalysis DOI

Pritesh Khobrekar,

Sandesh T. Bugde

Molecular Catalysis, Год журнала: 2025, Номер 582, С. 115169 - 115169

Опубликована: Май 8, 2025

Язык: Английский

Процитировано

0

Investigation of Heavy Atom Effects and pH Sensitivity on the Photocatalytic Cross-Dehydrogenative Coupling Reaction of Halogenated Fluorescein dyes DOI

Tingwei Cai,

Hanchang Hu,

Qiangqiang Zhao

и другие.

Dyes and Pigments, Год журнала: 2024, Номер 232, С. 112437 - 112437

Опубликована: Сен. 7, 2024

Язык: Английский

Процитировано

1

Visible Light‐Driven Glycosylation Mediated by Trifluoromethyl Thianthrenium Triflate with Thioglycoside Donors DOI
Guanghui Ni, Ruina Liu, Fei Zou

и другие.

European Journal of Organic Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Сен. 23, 2024

Abstract An efficient photoredox‐catalyzed glycosylation using a p ‐tolyl thioglycoside donor in the presence of trifluoromethyl thianthrenium triflate (TT‐CF 3 + TfO − ) has been investigated. This approach involves generating radical via single electron transfer between TT‐CF and photocatalyst Rose Bengal, thereby activating thioglycosides facilitating glycosylation. method operates under mild reaction conditions tolerates variety functional groups.

Язык: Английский

Процитировано

0

Synthesis of diarylsulphide/diarylselenide embedded pyrazole-fused isocoumarins and isatin/ninhydrin hydrazones via acid catalyzed solvent and temperature controlled reactions DOI
Sayanwita Panja,

Arun Dhurey,

Animesh Pramanik

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 11, 2024

Room temperature stirring of a mixture chalcogenated arylhydrazones and ninhydrin in dichloromethane (DCM) the presence acid leads to formation pyrazole-fused isocoumarins, substituted with diarylsulphide/diarylselenide moiety. On other hand, refluxing same protic polar solvent ethanol produces containing hydrazones. Further study reveals that, like ninhydrin, isatin can also generate corresponding hydrazones at C-3 position under similar reaction conditions.

Язык: Английский

Процитировано

0