Photoredox‐Catalyzed Three‐Component Difluoroalkylation of Quinoxalin‐2(1H)‐ones with Unactivated Vinylarenes and [Ph3PCF2H]+Br DOI
Yuandong Xu,

Hongzhao Qu,

Jinwei Yuan

et al.

Asian Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: 12(11)

Published: Sept. 12, 2023

Abstract An efficient synthesis of a variety 3‐difluoroalkyl quinoxalin‐2(1 H )‐ones via photoredox‐catalyzed three‐component reaction between )‐ones, vinylarenes, with inexpensive and easily accessible difluoromethyltriphenyl phosphonium bromide salt as the difluoromethylated reagent is described. This protocol shows excellent reactivity, providing wide range difluoroalkyl‐substituted in moderate to yields under mild conditions. A difluoroalkyl radical intermediate was involved this transformation.

Language: Английский

Photoinduced, additive- and photosensitizer-free multi-component synthesis of naphthoselenazol-2-amines with air in water DOI

Hong‐Tao Ji,

Keli Wang, Wen‐Tao Ouyang

et al.

Green Chemistry, Journal Year: 2023, Volume and Issue: 25(20), P. 7983 - 7987

Published: Jan. 1, 2023

An atom- and step-economical, efficient eco-friendly method for constructing naphthoselenazol-2-amines through a visible-light photocatalytic multi-component reaction under aqueous phase conditions is reported.

Language: Английский

Citations

71

Multicomponent Synthesis of Alkyl BCP-Heteroaryls via Electron Donor–Acceptor Complex Photoactivation under Mild Conditions DOI
Yanhe Li, Jun Xu, Yuxin Wang

et al.

The Journal of Organic Chemistry, Journal Year: 2025, Volume and Issue: 90(4), P. 1683 - 1696

Published: Jan. 17, 2025

In the vanguard of sustainable chemistry, pursuit efficient pathways for synthesis alkyl bicyclo[1.1.1]pentane-heteroaryls has captured attention scientific vanguard. We herein report a groundbreaking and eco-conscious multicomponent coupling reaction that paves way alkylation heteroarylation [1.1.1]propellane, process uniquely enabled by photochemical prowess an electron donor–acceptor (EDA) complex. This method is distinguished its minimalist yet powerful approach: devoid transition metals, additives, photosensitizers. Its universality further exemplified seamless compatibility broad spectrum halides heteroarenes under standardized conditions, heralding new era synthetic versatility. The method's practicality underscored capacity late-stage modification pharmaceuticals, offering transformative tool enhancement existing drug molecules. Moreover, facile derivatization synthesized products underscores adaptability potential diverse applications. Our mechanistic studies have elucidated underlying radical-relay pathway, pinpointing pivotal role EDA complex in initiating transformation. discovery not only enriches our fundamental understanding but also opens avenues strategic optimization.

Language: Английский

Citations

2

Three‐Component Reactions of Quinoxalin‐2(1H)‐ones: Recent Advances DOI Open Access
Keli Wang,

Hong‐Tao Ji,

Li‐Juan Ou

et al.

European Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: unknown

Published: Sept. 11, 2023

Abstract The multicomponent reactions of quinoxalin‐2(1 H )‐ones has attracted considerable interest due to their significant biological and chemical activities. very recent advances (from 2021 the beginning 2023) on radical three‐component cascade reaction )‐one derivatives at C3 position were summarized in this mini‐review. According kind types involved, some representative examples detailed mechanism have been categorized discussed. red front was covered by Figure 1.

Language: Английский

Citations

36

Enantioselective Chemodivergent Three-Component Radical Tandem Reactions through Asymmetric Photoredox Catalysis DOI

Chaorui Ma,

Jingyu Shen,

Chaofan Qu

et al.

Journal of the American Chemical Society, Journal Year: 2023, Volume and Issue: 145(36), P. 20141 - 20148

Published: Aug. 28, 2023

Chemodivergent synthesis has been achieved in asymmetric photocatalysis. Under a dual catalyst system consisting of chiral phosphoric acid and DPZ as photosensitizer, different inorganic bases enabled the formation two sets valuable products from three-component radical tandem transformations 2-bromo-1-arylenthan-1-ones, styrenes, quinoxalin-2(1H)-ones. The key to success was distinct pKa environment, which radicals that formed on quinoxalin-2(1H)-one rings after addition processes underwent either single-electron oxidation or reduction. In addition, this work represents first use quinoxalin-2(1H)-ones photoredox catalysis.

Language: Английский

Citations

29

Transition-metal-, oxidant- and additive-free multi-component synthesis of alkyl heteroaryl BCPs enabled by visible-light-induced phosphine-catalyzed halogen-atom transfer DOI
Jun Xu,

Yu Hong,

Ruiyuan Xu

et al.

Organic Chemistry Frontiers, Journal Year: 2024, Volume and Issue: unknown

Published: Jan. 1, 2024

This study describes a pioneering visible-light-induced phosphine-catalyzed halogen-atom transfer (XAT) strategy that heralds new era in the difunctionalization of [1.1.1]propellane.

Language: Английский

Citations

12

Photoinduced Dehydrogenative Amination of Quinoxalin-2(1H)-ones with Air as an Oxidant DOI

Haoran Jiao,

Yue Jing,

Kaikai Niu

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(8), P. 5371 - 5381

Published: March 29, 2024

A facile and eco-friendly photoinduced dehydrogenative amination of quinoxalin-2(1H)-ones with aliphatic amines without any metal, strong oxidant, photocatalyst has been established for the first time. This reaction proceeding efficiently air as sole oxidant at room temperature obtains a wide range 3-aminoquinoxaline-2(1H)-ones in high yields excellent functional group tolerance. The mechanistic studies show an interesting involvement photosensitizer, which eliminates requirement external photocatalysts.

Language: Английский

Citations

8

Light‐Induced Domino and Multicomponent Reactions: How to Reach Molecular Complexity without a Catalyst DOI Creative Commons
Polyssena Renzi, Jacopo Scarfiello, Alberto Lanfranco

et al.

European Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: unknown

Published: Aug. 31, 2023

Abstract Achieving high molecular complexity can be not trivial, but the exploitation of domino reactions provides an atom‐ and step‐economical method to reach this target. Over past decades, a lot efforts have been put on development photocatalytic cascades employing both metal‐based purely organic catalysts. Despite effectiveness these protocols, catalyst‐ additive‐free light‐induced are gaining momentum thank their efficiency, operational simplicity sustainability. The increasing number papers published field in last years is proof appeal transformations. In Review, we discuss multicomponent mediated by light with focus photocatalyst‐ processes. most recent advances synthesis complex nitrogen‐, oxygen‐, sulphur‐ selenium‐heterocycles together analysed emphasis experimental mechanistic studies.

Language: Английский

Citations

10

Self-photocatalyzed three-component radical cascade reaction of quinoxalinones, simple alkenes and zhdankin reagent DOI
Xiaoyun Sun, Wenhao Liu, Xingyuan Liu

et al.

Molecular Catalysis, Journal Year: 2024, Volume and Issue: 557, P. 113981 - 113981

Published: March 1, 2024

Language: Английский

Citations

3

Visible Light-Induced Radical Cascade Functionalization of Quinoxalin-2(1H)-ones: Three-Component 1,2-Di(hetero)arylation Approach with Styrenes and Thianthrenium Salts DOI

Sudip Sau,

Shinobu Takizawa, Hun Young Kim

et al.

Organic Letters, Journal Year: 2024, Volume and Issue: 26(41), P. 8821 - 8826

Published: Oct. 9, 2024

The additive-free visible light-induced three-component 1,2-di(hetero)arylation of styrenes was developed using quinoxalin-2(1

Language: Английский

Citations

3

C─H Functionalization of Heteroarenes via Electron Donor‐Acceptor Complex Photoactivation DOI
Alakananda Hajra,

Madhusudan Mondal,

Sumit Ghosh

et al.

ChemSusChem, Journal Year: 2024, Volume and Issue: unknown

Published: July 8, 2024

C-H Functionalization of heteroarenes stands as a potent instrument in organic synthesis, and with the incorporation visible light, it emerged transformative game-changer. In this domain, electron donor-acceptor (EDA) complex, formed through pairing an electron-rich substrate electron-accepting molecule, has garnered substantial consideration recent years due to related avoidance requirement photocatalyst well oxidant. EDA complexes can undergo photoactivation under mild conditions exhibit high functional group tolerance, making them potentially suitable for functionalization biologically relevant heteroarenes. This review article provides overview advancements field via complex literature coverage up April, 2024.

Language: Английский

Citations

2