Visible-Light-Induced Trifluoromethyl Radical Addition to Thiocarbonyl of Thioamide Derivatives DOI

Yuanyuan Ren,

Yuxiu Zhou,

Ke‐Hu Wang

и другие.

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

Опубликована: Фев. 28, 2025

An effective trifluoromethyl radical addition to the thiocarbonyl of thioamide derivatives is described, which produces various trifluoromethylthiolated N-heterocycles such as 6-(trifluoromethylthio)phenanthridine, 2-(trifluoromethylthio)indole, and 2-(trifluoromethylthio)benzothiazole under visible-light irradiation. The process features advantages mild reaction conditions, a cheap easily available source (CF3Br), green energy, well broad substrate scope. mechanism investigated in detail, scale-up experiments are performed.

Язык: Английский

Recent advances in the synthesis of trifluoromethyl-containing heterocyclic compounds via trifluoromethyl building blocks DOI

Yaopeng Liu,

Qingyu Tian,

Jin Ge

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(31), С. 6246 - 6276

Опубликована: Янв. 1, 2024

Recent advances in the preparation of trifluoromethyl-containing heterocyclics via trifluoromethyl building block strategies over period from 2019 to present are systematically summarized and discussed.

Язык: Английский

Процитировано

12

[3 + 2] Cycloaddition Reaction of Vinylsulfonium Salts with Hydrazonoyl Halides: Synthesis of Pyrazoles DOI

Wen-Jing Luo,

Xiuwen Liang,

Maizhuo Chen

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(14), С. 10066 - 10076

Опубликована: Июль 2, 2024

An efficient [3 + 2] cycloaddition reaction between in situ generated nitrile imines from hydrazonoyl halides and vinylsulfonium salts is developed. The are demonstrated to be a new class of partner for conduct the reaction. process provides concise method construction pyrazole derivatives under mild conditions with broad substrate scope, good product yields, high regioselectivity.

Язык: Английский

Процитировано

6

Visible-Light-Induced Trifluoromethyl Radical Addition to Thiocarbonyl of Thioamide Derivatives DOI

Yuanyuan Ren,

Yuxiu Zhou,

Ke‐Hu Wang

и другие.

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

Опубликована: Фев. 28, 2025

An effective trifluoromethyl radical addition to the thiocarbonyl of thioamide derivatives is described, which produces various trifluoromethylthiolated N-heterocycles such as 6-(trifluoromethylthio)phenanthridine, 2-(trifluoromethylthio)indole, and 2-(trifluoromethylthio)benzothiazole under visible-light irradiation. The process features advantages mild reaction conditions, a cheap easily available source (CF3Br), green energy, well broad substrate scope. mechanism investigated in detail, scale-up experiments are performed.

Язык: Английский

Процитировано

0