Blue Light-Emitting Diode-Induced Direct C–H Functionalization of 1,4-Quinones with Aryl and Alkyl Boronic Acids DOI
Souvik Guha,

Tejas Prabakar,

Subhabrata Sen

и другие.

The Journal of Organic Chemistry, Год журнала: 2022, Номер 87(22), С. 15421 - 15434

Опубликована: Ноя. 2, 2022

A direct functionalization of numerous 1,4-quinones with various aryl boronic acids is reported under blue light-emitting diodes (LEDs). This reaction occurs at room temperature in an open flask without any catalysts, base, and oxidants acetonitrile (ACN) scalable grams. With diverse like 1,4-benzo-, naphtho-, anthra-, 4-bromonaphthoquinones as substrates, facile cross coupling reactions occur alkyl assistance from photocatalysts. 2-Alkylated cyclohexene-1,4-diones were obtained when the reacted standard conditions. However, slight warming mixture afforded desired alkylated 1,4-quinones. The believed to proceed through LED-induced radical formation rings assisted by

Язык: Английский

External photocatalyst-free C-H alkylation of N-sulfonyl ketimines with alkanes under visible light DOI

Hai‐Yang Song,

Fang Xiao,

Jun Jiang

и другие.

Chinese Chemical Letters, Год журнала: 2023, Номер 34(9), С. 108509 - 108509

Опубликована: Апрель 28, 2023

Язык: Английский

Процитировано

53

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

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(8), С. 1708 - 1713

Опубликована: Янв. 1, 2024

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

Язык: Английский

Процитировано

26

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

Uncovering the Potential of Boronic Acid and Derivatives as Radical Source in Photo(electro)chemical Reactions DOI
Serena Pillitteri, Prabhat Ranjan, Erik V. Van der Eycken

и другие.

Advanced Synthesis & Catalysis, Год журнала: 2022, Номер 364(10), С. 1643 - 1665

Опубликована: Апрель 25, 2022

Abstract The chemistry of boron compounds has been profoundly investigated in the last decades, leading to ubiquity many synthetic applications as well biologically active molecules. Since advent photoredox catalysis, an upsurge discovery suitable radical precursors witnessed, and is becoming a protagonist this field. Despite studies focused on trifluoroborates, use boronic acids esters have received much less attention regard. Because their high oxidation potential, development methods enable involvement photocatalyzed reactions only recent. Nonetheless, review summarizes novel strategies developed unlock role photochemical discloses potential that own, when intrinsic chemical properties are exploited. magnified image

Язык: Английский

Процитировано

53

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

Hong‐Tao Ji,

Li‐Juan Ou

и другие.

European Journal of Organic Chemistry, Год журнала: 2023, Номер unknown

Опубликована: Сен. 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.

Язык: Английский

Процитировано

37

NPh3-Mediated WO3-Photocatalyzed Semiheterogeneous Hydroxylation of Aryl and Alkyl Boronic Acids DOI
Xiaojun Huang,

Hong‐Tao Ji,

Xiao Li

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(15), С. 10654 - 10659

Опубликована: Июль 17, 2024

With an inexpensive and commercially available WO

Язык: Английский

Процитировано

14

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

Haoran Jiao,

Yue Jing,

Kaikai Niu

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(8), С. 5371 - 5381

Опубликована: Март 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.

Язык: Английский

Процитировано

9

Visible-light-induced novel cyclization of 2-(2-(arylethynyl)benzylidene)-malononitrile derivatives with 2,6-di(tert-butyl)-4-methylphenol to bridged spirocyclic compounds DOI
Xiaofei Xie, Lei Wang, Quan Zhou

и другие.

Chinese Chemical Letters, Год журнала: 2022, Номер 33(12), С. 5069 - 5073

Опубликована: Март 23, 2022

Язык: Английский

Процитировано

37

Visible light-mediated radical-cascade addition/cyclization of arylacrylamides with aldehydes to form quaternary oxindoles at room temperature DOI

Zhaozhao Sun,

Huawen Huang, Qiaolin Wang

и другие.

Organic Chemistry Frontiers, Год журнала: 2022, Номер 9(13), С. 3506 - 3514

Опубликована: Янв. 1, 2022

The visible light-induced oxidative radical cascade coupling of N -arylacrylamides with aldehydes using bromide as the hydrogen atom transfer agent to synthesize functional oxindoles is described.

Язык: Английский

Процитировано

31

Diverse catalytic systems for nitrogen-heterocycle formation from O-acyl ketoximes DOI Open Access
Zhonghua Qu,

Tong Tian,

Guo‐Jun Deng

и другие.

Chinese Chemical Letters, Год журнала: 2022, Номер 34(1), С. 107565 - 107565

Опубликована: Май 28, 2022

Язык: Английский

Процитировано

29