Electrocatalytic Three-Component Synthesis of 4-Bromopyrazoles from Acetylacetone, Hydrazine and Diethyl Bromomalonate DOI Open Access

Si‐Yu Mu,

Hongxia Li,

Zhilin Wu

и другие.

Chinese Journal of Organic Chemistry, Год журнала: 2022, Номер 42(12), С. 4292 - 4292

Опубликована: Янв. 1, 2022

Pyrazoles are the most important five-membered N-heterocycles as they present in many natural products and synthetic drugs.Among various pyrazole derivatives, 4-bromopyrazoles have attracted great attention because not only display significant biological activities physicochemical properties but also serve valuable synthons organic chemistry.In this manuscript, an efficient eco-friendly method for synthesis of through threecomponent reaction hydrazine, acetylacetone 2-bromomalonate was reported proposal mechanism revealed.According to mechanism, hydrazine reacts with afford firstly, which then converts 4-bromopyrazole bromination.This could be well applicable bromination other heterocyclic compounds.Given high oxidation state diethyl 2-bromomalonate, peroxidation can avoided electrolysis process, thus excess amount brominating agent required.

Язык: Английский

Visible light-induced Z-scheme V2O5/g-C3N4 heterojunction catalyzed cascade reaction of unactivated alkenes DOI
Qingwen Gui, Fan Teng, Peng Yu

и другие.

CHINESE JOURNAL OF CATALYSIS (CHINESE VERSION), Год журнала: 2022, Номер 44, С. 111 - 116

Опубликована: Дек. 2, 2022

Язык: Английский

Процитировано

80

Ferrocene/air double-mediated FeTiO3-photocatalyzed semi-heterogeneous annulation of quinoxalin-2(1H)-ones in EtOH/H2O DOI
Wen‐Tao Ouyang,

Hong‐Tao Ji,

Jun Jiang

и другие.

Chemical Communications, Год журнала: 2023, Номер 59(94), С. 14029 - 14032

Опубликована: Янв. 1, 2023

With both ferrocene and air as the redox catalysts, for first time, low-cost natural ilmenite (FeTiO3) was successfully used photocatalytic bond formations. Under assistance of a traceless H-bond, HCHO methylene reagent, variety imidazo[1,5-a]quinoxalinones were semi-heterogeneously photosynthesized in high yields with good functional group compatibility.

Язык: Английский

Процитировано

52

EtOH-catalyzed electrosynthesis of imidazolidine-fused sulfamidates fromN-sulfonyl ketimines,N-arylglycines and formaldehyde DOI
Yuhan Lu,

Si‐Yu Mu,

Hongxia Li

и другие.

Green Chemistry, Год журнала: 2023, Номер 25(14), С. 5539 - 5542

Опубликована: Янв. 1, 2023

With formaldehyde as an atom-economical carbonyl synthon, the EtOH-catalyzed electrochemical multicomponent synthesis of various imidazolidine-fused sulfamidates under organic oxidant-free, energy-saving and mild conditions was developed.

Язык: Английский

Процитировано

50

Transition-metal-free C–S bond cleavage and transformation of organosulfur compounds DOI
Ke Yang, Qin Li, Zhengyi Li

и другие.

Chemical Communications, Год журнала: 2023, Номер 59(36), С. 5343 - 5364

Опубликована: Янв. 1, 2023

The activation and transformation of organic chemical bonds is a fundamental scientific problem. In the past several decades, C-S bond cleavage for construction C-C C-heteroatom has received tremendous attention in chemistry. Although significant progress been made field transition metal strategies, variety novel transition-metal-free strategies have also developed using halogenated reagents, oxidants, acids, bases. Moreover, photochemical electrochemical methods to achieve organosulfur compounds. To date, however, no comprehensive review reported. Therefore, we herein provide major advances compounds, including thioethers, sulfoxides, sulfones, thioacetals, sulfonium salts, sulfur ylides.

Язык: Английский

Процитировано

42

Electrochemical regioselective synthesis of N-substituted/unsubstituted 4-selanylisoquinolin-1(2H)-ones DOI

Zhilin Wu,

Jinyang Chen,

Xian-Zhi Tian

и другие.

Chinese Chemical Letters, Год журнала: 2021, Номер 33(3), С. 1501 - 1504

Опубликована: Авг. 19, 2021

Язык: Английский

Процитировано

79

TBAI/H2O-cooperative electrocatalytic decarboxylation coupling-annulation of quinoxalin-2(1H)-ones with N-arylglycines DOI
Yuhan Lu,

Zhuo-Tao Zhang,

Hongyu Wu

и другие.

Chinese Chemical Letters, Год журнала: 2022, Номер 34(7), С. 108036 - 108036

Опубликована: Дек. 5, 2022

Язык: Английский

Процитировано

64

Electrochemically mediated decarboxylative acylation of N-nitrosoanilines with α-oxocarboxylic acids DOI Creative Commons
Xinyu Wang,

Shihong Wu,

Yujing Zhong

и другие.

Chinese Chemical Letters, Год журнала: 2022, Номер 34(2), С. 107537 - 107537

Опубликована: Май 19, 2022

Язык: Английский

Процитировано

42

Electrochemical radical annulation of 2-alkynyl biaryls with diselenides under catalyst- and chemical oxidant-free conditions DOI

Jun Jiang,

Keli Wang, Xiao Li

и другие.

Chinese Chemical Letters, Год журнала: 2023, Номер 34(12), С. 108699 - 108699

Опубликована: Июнь 17, 2023

Язык: Английский

Процитировано

26

External electrolyte-free electrochemical one-pot cascade synthesis of 4-thiocyanato-1H-pyrazoles DOI

Wei-Bao He,

Sai-Jie Zhao,

Jingyang Chen

и другие.

Chinese Chemical Letters, Год журнала: 2022, Номер 34(2), С. 107640 - 107640

Опубликована: Июнь 30, 2022

Язык: Английский

Процитировано

34

Electrochemically mediated three-component synthesis of isothioureas using thiols as sulfur source DOI Creative Commons
Mu‐Xue He, Ping‐Fu Zhong,

Hanfu Liu

и другие.

Green Synthesis and Catalysis, Год журнала: 2022, Номер 4(1), С. 41 - 45

Опубликована: Март 4, 2022

The simultaneous binding/dissociation of multiple bonds in a one-pot manner by multicomponent reactions provide an important approach for developing novel and sustainable pathway the drug discovery process. Herein we develop electrocatalytic three-component reaction to construct multifunctional valuable isothiourea compounds, which uses thiols, isocyanides amines as substrates. Compared with previous work, organic electrosynthesis technique can avoid requirement heavy metal catalysts stoichiometric oxidants. In addition, using thiol substrate participate broadens source sulfur, also more abundant derivatives.

Язык: Английский

Процитировано

28