Synthesis of Sulfenamides via Photoredox N–S Coupling of Dialkyl Azodicarboxylates and Thiols DOI
Qun Liu,

Xiaoyun Feng,

Fang Xie

и другие.

Organic Letters, Год журнала: 2024, Номер unknown

Опубликована: Дек. 27, 2024

We herein report a photoredox N–S coupling reaction between dialkyl azodicarboxylates and thiols to access sulfenamide scaffolds. This proceeds under mild, green, operationally simple conditions, offering broad scope of sulfenamides with high yields excellent atom efficiency. Mechanistic investigations revealed this followed photoinitiated radical pathway in which iodide plays crucial role as both initiator single-electron reductant.

Язык: Английский

Application of a fluorescent probe exhibiting a large stokes shift after the precise detection of hydrazine in plants, foods and living cells DOI
Yan Zhang,

Huang Yan,

Guiyi Yang

и другие.

Journal of Hazardous Materials, Год журнала: 2025, Номер 488, С. 137452 - 137452

Опубликована: Фев. 3, 2025

Язык: Английский

Процитировано

2
Synthesis of Sulfenamides via Photoredox N–S Coupling of Dialkyl Azodicarboxylates and Thiols DOI
Qun Liu,

Xiaoyun Feng,

Fang Xie

и другие.

Organic Letters, Год журнала: 2024, Номер unknown

Опубликована: Дек. 27, 2024

We herein report a photoredox N–S coupling reaction between dialkyl azodicarboxylates and thiols to access sulfenamide scaffolds. This proceeds under mild, green, operationally simple conditions, offering broad scope of sulfenamides with high yields excellent atom efficiency. Mechanistic investigations revealed this followed photoinitiated radical pathway in which iodide plays crucial role as both initiator single-electron reductant.

Язык: Английский

Процитировано

2