Photocatalytic Consecutive Photoinduced Electron Transfer-Enabled C(sp3)–H Pyridylation of Dihydroquinoxalin-2-ones DOI
Changduo Pan, Dongdong Chen

The Journal of Organic Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 22, 2024

A photocatalytic decyanative C(sp3)–H pyridination of dihydroquinoxalin-2-ones with 4-cyanopyridines was developed by utilizing 4CzIPN as the photocatalyst. Mechanism studies show that this organophotocatalytic direct undergoes a radical–radical cross-coupling pathway promoted consecutive photoinduced electron transfer.

Язык: Английский

Phototriggered Self-Catalyzed Phosphorylation of 3,4-Dihydroquinoxalin-2(1H)-ones with Diarylphosphine Oxides in EtOH DOI
Yanfang Jiang, Wen‐Tao Ouyang,

Hong‐Tao Ji

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Сен. 19, 2024

A highly effective external photocatalyst- and additive-free method for the phosphorylation of 3,4-dihydroquinoxalin-2(1

Язык: Английский

Процитировано

12

Nd@C3N4-photoredox/chlorine dual catalyzed synthesis and evaluation of antitumor activities of 4-alkylated sulfonyl ketimines DOI

Hong‐Tao Ji,

Yuhan Lu, Yanting Liu

и другие.

Chinese Chemical Letters, Год журнала: 2024, Номер unknown, С. 110568 - 110568

Опубликована: Окт. 1, 2024

Язык: Английский

Процитировано

5

Electron-Donor-Mediated Divergent Transformation of Br–RF via EDA Complex for the Synthesis of Fluorine-Containing Oxindoles and Amides DOI
Shupeng Zhang,

Jin-Xin Lan,

Mei-Ling Yang

и другие.

Organic Letters, Год журнала: 2024, Номер 26(46), С. 9990 - 9995

Опубликована: Ноя. 11, 2024

We have developed an unprecedented electron-donor-controlled divergent reaction between

Язык: Английский

Процитировано

4

Photoredox-Catalyzed Three-Component Sulfonaminoalkynylation of Alkenes via a Radial/Polar Crossover DOI

Lixian Shen,

Jie Liu, Peng Xue

и другие.

The Journal of Organic Chemistry, Год журнала: 2025, Номер 90(4), С. 1656 - 1662

Опубликована: Янв. 21, 2025

We report a photoredox-catalyzed three-component sulfonaminoalkynylation of alkenes with N-aminopyridine salts and potassium alkynyltrifluoroborate salts. This aminoalkylation reaction underwent radial/polar crossover mechanism, which was distinguished from the previous reports. A variety β-alkynylated sulfonamides were obtained in moderate to excellent yields. The versatility this method further evidenced by its successful application modifying biological molecules advanced stages development.

Язык: Английский

Процитировано

0

Polymer-Supported Selenium Affording Opportunities in Catalyst Design DOI
Guanghui Yuan, Xu Zhang, Lei Yu

и другие.

The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Фев. 20, 2025

Polymer-supported selenium has been reported as a heterogeneous catalyst that is easily separated from the reaction system, thereby making recovery and reuse of more convenient. However, utilization polymer-supported in preparation catalysts not restricted to aforementioned technical advantages. Recent studies have shown small-molecule organoselenium significant performance differences, leading distinct mechanisms, which offer opportunities for development new organic reactions.

Язык: Английский

Процитировано

0

g-C3N4-Based Heterogeneous Photocatalyzed Synthesis and Evaluation of Antitumor Activities of Fluoroalkylated 4H-Pyrido[1,2-a]pyrimidin-4-ones DOI
Ningbo Li, Yan Liu,

Chu-Qian Hu

и другие.

The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Фев. 26, 2025

The first example of heterogeneous photoredox-catalyzed fluoroalkylation 4H-pyrido[1,2-a]pyrimidin-4-ones has been developed. With low-cost commercial g-C3N4 as the recyclable photocatalyst and cheap sodium fluoroalkyl sulfonates source, a variety fluoroalkylated pyridopyrimidinones were constructed in moderate to high yields. present reaction can be easily scaled up with good efficiency, catalytic system reused 5 times slight loss activities. Furthermore, biological activity synthesized compounds was preliminarily investigated.

Язык: Английский

Процитировано

0

Self-Catalyzed Sono-Photoinduced Arylation of Quinoxalin-2(1H)-ones with Arylhydrazines DOI

Yao-Dan Xu,

Yang Xing,

Hong‐Tao Ji

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Ноя. 25, 2024

Herein, the first example of self-catalyzed sono-photoinduced carbon-carbon bond formation was described. Combining advantages phototriggered self-catalysis and ultrasonic catalysis, a wide range 3-arylquinoxalin-2(1

Язык: Английский

Процитировано

3

Decatungstate-photocatalyzed tandem acylation/cyclization/self-hydrogenation of isocyanides with aldehydes to hydroxyalkylated N-heteroarenes via multiple hydrogen atom transfer DOI

Hong‐Tao Ji,

Qiong-Hui Peng,

Jiasheng Wang

и другие.

Green Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Янв. 1, 2024

A 100% atom economical construction of hydroxyalkylated N-heteroarenes through decatungstate-catalyzed tandem cyclization/self-hydrogenation isocyanides and aldehydes under exogenous hydrogen reagent- byproduct-free conditions was developed.

Язык: Английский

Процитировано

2

Dual Ce@g-C3N4-Photoredox/Chlorine Catalysis: Cross-Dehydrogenative Coupling of N-Heteroarenes and Alkanes/Ethers with H2 Evolution DOI

Hong‐Tao Ji,

Yu-Qi Tang,

Yaohui Wang

и другие.

Organic Letters, Год журнала: 2024, Номер 26(46), С. 9822 - 9827

Опубликована: Ноя. 11, 2024

With Ce@g-C

Язык: Английский

Процитировано

2

Recyclable Ag/g‐C3N4 Catalyzed Visible‐light Promoted Heterogeneous Synthesis of Unsymmetric Diaryl Chalcogenides DOI

Hong‐Tao Ji,

Yunchao Yi,

Min‐Hang Zhou

и другие.

Asian Journal of Organic Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Окт. 27, 2024

Abstract With Ag/g‐C 3 N 4 semiconductor as the heterogeneous photocatalyst, visible light promoted synthesis of unsymmetric diaryl chalcogenides could be achieved under additive‐free and mild conditions. A series were generated in good to excellent yields with high functional group tolerance. The photocatalyst is easily recovered from reaction mixture reused at least 5 times, opening way for larger‐scale industrial applications this type photocatalytic bond‐forming reactions.

Язык: Английский

Процитировано

1