Visible-Light-Promoted Polysubstituted Olefins Synthesis Involving Sulfur Ylides as Carbene Trapping Reagents DOI
Cong Ye, Bao‐Gui Cai,

Juan Lü

et al.

The Journal of Organic Chemistry, Journal Year: 2020, Volume and Issue: 86(1), P. 1012 - 1022

Published: Dec. 10, 2020

A blue-light-emitting diode (LED) promoted coupling of aryl diazoacetates with sulfur ylides is described. This protocol features mild conditions, good functional group tolerance, and broad substrate scope for both ylides. Under optimal reaction a wide range trisubstituted olefins obtained in moderate to yield, which can be further transferred other biologically important heterocycles after two-step simple operation.

Language: Английский

Photo-/electrocatalytic functionalization of quinoxalin-2(1H)-ones DOI
Kai Sun, Fang Xiao, Bing Yu

et al.

CHINESE JOURNAL OF CATALYSIS (CHINESE VERSION), Journal Year: 2021, Volume and Issue: 42(11), P. 1921 - 1943

Published: Aug. 30, 2021

Language: Английский

Citations

137

Visible-light-induced four-component difunctionalization of alkenes to construct phosphorodithioate-containing quinoxalin-2(1H)-ones DOI
Xiao‐Ming Chen,

Lianhui Song,

Jun Pan

et al.

Chinese Chemical Letters, Journal Year: 2024, Volume and Issue: 35(11), P. 110112 - 110112

Published: June 25, 2024

Language: Английский

Citations

28

Radical relay cyclization/C–C bond formation of allyloxy-tethered aryl iodides with quinoxalin-2(1H)-ones via polysulfide anion photocatalysis DOI
Zhongyi Zhang, Yaqin Zhou, Jiehui Wang

et al.

Organic & Biomolecular Chemistry, Journal Year: 2024, Volume and Issue: 22(8), P. 1708 - 1713

Published: Jan. 1, 2024

A visible-light-induced radical relay cyclization/C-C bond formation of quinoxalin-2(1

Language: Английский

Citations

26

Aryl acyl peroxides for visible-light induced decarboxylative arylation of quinoxalin-2(1H)-ones under additive-, metal catalyst-, and external photosensitizer-free and ambient conditions DOI
Long‐Yong Xie, Sha Peng, Lihua Yang

et al.

Green Chemistry, Journal Year: 2020, Volume and Issue: 23(1), P. 374 - 378

Published: Oct. 23, 2020

Aryl radicals were generated for the first time from aryl acyl peroxides in ethyl acetate under ambient conditions and visible-light illumination absence of any additive, metal catalyst, or external photosensitizer.

Language: Английский

Citations

121

Divergent Synthesis of Aziridine and Imidazolidine Frameworks under Blue LED Irradiation DOI
Xiao Cheng, Bao‐Gui Cai, Hui Mao

et al.

Organic Letters, Journal Year: 2021, Volume and Issue: 23(11), P. 4109 - 4114

Published: May 14, 2021

We develop a visible light-promoted divergent cycloaddition of α-diazo esters with hexahydro-1,3,5-triazines, leading to series aziridine and imidazolidine frameworks in average good yield, by simply changing the reaction media used. It is noteworthy that occurs under sole light irradiation without need for exogenous photoredox catalysts. More significantly, reasonable mechanism was proposed on basis control experiments density functional theory calculation results.

Language: Английский

Citations

69

Visible-light-promoted catalyst-/additive-free synthesis of aroylated heterocycles in a sustainable solvent DOI

Fan‐Lin Zeng,

Kunchen Xie,

Yuting Liu

et al.

Green Chemistry, Journal Year: 2022, Volume and Issue: 24(4), P. 1732 - 1737

Published: Jan. 1, 2022

A general visible-light-induced catalyst-/additive-free strategy was developed for the construction of various aroylated heterocyclesunder air and room temperature conditions.

Language: Английский

Citations

54

Photoinduced Ligand‐to‐Metal Charge Transfer of Carboxylates: Decarboxylative Functionalizations, Lactonizations, and Rearrangements DOI Creative Commons

Sigrid Gavelle,

Milan Innocent,

Thomas Aubineau

et al.

Advanced Synthesis & Catalysis, Journal Year: 2022, Volume and Issue: 364(24), P. 4189 - 4230

Published: Dec. 3, 2022

Abstract In the quest for sustainable processes, selection of resources and catalysts is central importance. Carboxylic acids, which are abundant, stable ideally biobased feedstocks, can be considered as attractive platforms towards a range functionalized molecules. A recent resurgence photoinduced ligand‐to‐metal charge transfer (LMCT) carboxylates led to tremendous developments in field earth‐abundant metal mediated, visible‐light induced (non)‐decarboxylative transformations carboxylic acids. These reactions combine use available starting materials, low‐consuming energy source abundant catalysts. Besides these undeniable advantages, they also provide mild, highly selective innovative conditions complex molecule functionalization. The objective this review give an overview advances LMCT with special focus on mechanistic aspects transformations. magnified image

Language: Английский

Citations

53

Direct benzylation reactions from benzyl halides enabled by transition-metal-free photocatalysis DOI

Panjie Xiang,

Kai Sun, Shuang Wang

et al.

Chinese Chemical Letters, Journal Year: 2022, Volume and Issue: 33(12), P. 5074 - 5079

Published: March 26, 2022

Language: Английский

Citations

49

Exploiting photoredox catalysis for carbohydrate modification through C–H and C–C bond activation DOI
Andrey Shatskiy, Elena V. Stepanova, Markus D. Kärkäs

et al.

Nature Reviews Chemistry, Journal Year: 2022, Volume and Issue: 6(11), P. 782 - 805

Published: Sept. 21, 2022

Language: Английский

Citations

49

Photoinduced Three-Component Difluoroalkylation of Quinoxalinones with Alkenes via Difluoroiodane(III) Reagents DOI

Ningning Zhou,

Ruiyue Liu,

Chunmeng Zhang

et al.

Organic Letters, Journal Year: 2022, Volume and Issue: 24(19), P. 3576 - 3581

Published: May 12, 2022

An environmentally friendly strategy for the photocatalyzed three-component reaction between quinoxalinones, alkenes, and hypervalent iodine(III) reagents is disclosed. The new designed difluoroiodane(III) reagent shows excellent reactivity, providing a wide range of difluoroalkyl-substituted quinoxaline-2(1H)-ones in moderate to yields under mild conditions. Experimental studies demonstrated that difluoroalkyl radical intermediate was involved this reaction.

Language: Английский

Citations

48