Access to Ketones via Nickel-Catalyzed Coupling between S-2-Pyridyl Thioesters and Redox-Active Esters Using an Organic Reductant DOI
Jianghong Liu, Zeyu Tian,

Zhen-Ye Wu

и другие.

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

Опубликована: Ноя. 15, 2024

A nickel-catalyzed coupling between S-2-pyridyl thioesters and redox-active esters has been reported. Diludine was used as a reductant in this strategy. Our method rapidly achieves the target ketone products moderate to good yield. The construction of nonanomeric C-acyl glycosides realized through approach well.

Язык: Английский

Molybdenum iron carbide-copper hybrid as efficient electrooxidation catalyst for oxygen evolution reaction and synthesis of cinnamaldehyde/benzalacetone DOI
Jinzhou Li,

Lange Du,

Songtao Guo

и другие.

Journal of Colloid and Interface Science, Год журнала: 2024, Номер 673, С. 616 - 627

Опубликована: Июнь 17, 2024

Язык: Английский

Процитировано

7
Access to Ketones via Nickel-Catalyzed Coupling between S-2-Pyridyl Thioesters and Redox-Active Esters Using an Organic Reductant DOI
Jianghong Liu, Zeyu Tian,

Zhen-Ye Wu

и другие.

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

Опубликована: Ноя. 15, 2024

A nickel-catalyzed coupling between S-2-pyridyl thioesters and redox-active esters has been reported. Diludine was used as a reductant in this strategy. Our method rapidly achieves the target ketone products moderate to good yield. The construction of nonanomeric C-acyl glycosides realized through approach well.

Язык: Английский

Процитировано

0