Electrochemical Synthesis of Selenosulfonates from Diselenides and Sulfonyl Hydrazides DOI

Jin-Feng Lv,

Yang Deng, Xinyi Liang

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(6), P. 3931 - 3940

Published: March 7, 2024

The electrochemical oxidative radical–radical cross-coupling of sulfonyl hydrazides with diselenides for the synthesis selenosulfonates was successfully accomplished. method is applicable to a wide range aromatic/aliphatic and diselenides, providing products in good excellent yields. Notably, this protocol stands out its green sustainable nature, as it does not rely on transition metals oxidizing agents, starting materials are cost-effective readily available.

Language: Английский

Photochemical Radical Cascade 6‐endo Cyclization of Dienes with α‐Carbonyl Bromides for the Synthesis of Six‐Membered Benzo‐Fused Lactams DOI

Jia‐Li Sui,

Yang Guo, Biquan Xiong

et al.

Chinese Journal of Chemistry, Journal Year: 2024, Volume and Issue: 42(19), P. 2323 - 2328

Published: May 22, 2024

Comprehensive Summary A novel visible‐light‐induced radical cascade 6‐ endo cyclization of dienes ( N ‐(2‐vinylphenyl)acryl amides) is developed utilizing α‐carbonyl bromides as alkyl reagents. This approach affords an efficient way for synthesizing six‐membered benzo‐fused lactam derivatives with chemo‐ and regio‐selectivity good functional group tolerance. Primary, secondary, tertiary are well‐compatible this reaction.

Language: Английский

Citations

2

Photo-Induced Difluoromethylation-Cyclization and Domino Amination-Defluorination to 4-(Aminomethyl)-3-fluoro-quinolinones DOI
Xin Wang, Dongyang Zhao,

Jia-Bo Huang

et al.

Organic Letters, Journal Year: 2024, Volume and Issue: unknown

Published: Sept. 30, 2024

Herein, we report a visible light-induced difluoromethylation cyclization and subsequent amination-defluorination reaction. This protocol allows efficient to valuable 3-fluoro-quinolinones in moderate excellent yields. A sequential difluoromethylation-cyclization-amination-defluorination mechanism was proposed based on study. Further density functional theory (DFT) calculations revealed that the base K

Language: Английский

Citations

2

Photoinduced Regioselective Perfluoroalkylation/Cyclization Cascade of 3‐Aza‐1,5‐Dienes: Access to Pentasubstituted 3‐Perfluoroalkyl‐1,3‐Dihydropyrrol‐2‐Ones DOI
Ruihan Yang,

Danna Chen,

Shi‐Yi Lin

et al.

European Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: 26(31)

Published: July 12, 2023

Abstract A visible light‐induced perfluoroalkylative cyclization of 3‐aza‐1,5‐dienes leading to pentasubstituted 1,3‐dihydropyrrole‐2‐ones is presented. The reaction regiospecific, for the radical adds across acrylamido moiety, whereas enaminic double bond functions as a built‐in trap. It could be carried out on 2‐gram scale, and sunlight usable light source. Other virtues protocol include short time, low catalyst loading, mild conditions broad substrate scope.

Language: Английский

Citations

6

Visible-light-promoted cascade selenylative cyclization of 2-alkynylthioanisoles for the synthesis of seleno-benzothiophenes DOI
Zhanghong Wang, Jiale Li, Shupeng Zhang

et al.

Molecular Catalysis, Journal Year: 2023, Volume and Issue: 549, P. 113469 - 113469

Published: Aug. 25, 2023

Language: Английский

Citations

4

Electrochemical Synthesis of Selenosulfonates from Diselenides and Sulfonyl Hydrazides DOI

Jin-Feng Lv,

Yang Deng, Xinyi Liang

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(6), P. 3931 - 3940

Published: March 7, 2024

The electrochemical oxidative radical–radical cross-coupling of sulfonyl hydrazides with diselenides for the synthesis selenosulfonates was successfully accomplished. method is applicable to a wide range aromatic/aliphatic and diselenides, providing products in good excellent yields. Notably, this protocol stands out its green sustainable nature, as it does not rely on transition metals oxidizing agents, starting materials are cost-effective readily available.

Language: Английский

Citations

1