Cu(I)-Catalyzed Three-Component Annulation for the Synthesis of 3-Acyl Imidazo[1, 5-a]Pyridines from 2-Pyridinyl-Substituted p-Quinone Methides, Terminal Alkynes, and TsN3 Using O2 as the Oxygen Source DOI
Yan Chen, Yuan‐Ting Zhang, Kun‐Peng Wang

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(8), С. 5423 - 5433

Опубликована: Апрель 1, 2024

Currently, most conventional methods to achieve imidazo[1,5-a]pyridines have limitations for the synthesis of 3-acyl imidazo[1,5-a]pyridines. Herein, a novel and efficient Cu(I)-catalyzed three-component annulation method valuable by reaction 2-pyridinyl-substituted p-QMs, terminal alkynes, TsN3 in presence O2 under mild conditions successfully been developed. The investigation indicated that molecular oxygen (O2) TsN3, respectively, serving as nitrogen sources, were essential successful completion system.

Язык: Английский

Electrochemical Oxidative Reassembly of 1,3-Diketones with Aryl Alkenes and Water via Carbon–Carbon Bond Cleavage Rearrangement DOI
Wei Wu,

R.K. Linghu,

Bingjie Jian

и другие.

Organic Letters, Год журнала: 2025, Номер unknown

Опубликована: Апрель 25, 2025

We report the electrochemical cleavage and reassembly of 1,3-diketones with aryl alkenes water for synthesis 1,4-ketoalcohol derivatives. This approach represents first example formal carbon-carbon alkene insertion via electro-oxidation, enabling direct diverse derivatives in good to high yields. The developed strategy employs an using inexpensive commercial carbon electrodes undivided cell under mild operationally simple conditions.

Язык: Английский

Процитировано

0

Cu(I)-Catalyzed Three-Component Annulation for the Synthesis of 3-Acyl Imidazo[1, 5-a]Pyridines from 2-Pyridinyl-Substituted p-Quinone Methides, Terminal Alkynes, and TsN3 Using O2 as the Oxygen Source DOI
Yan Chen, Yuan‐Ting Zhang, Kun‐Peng Wang

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(8), С. 5423 - 5433

Опубликована: Апрель 1, 2024

Currently, most conventional methods to achieve imidazo[1,5-a]pyridines have limitations for the synthesis of 3-acyl imidazo[1,5-a]pyridines. Herein, a novel and efficient Cu(I)-catalyzed three-component annulation method valuable by reaction 2-pyridinyl-substituted p-QMs, terminal alkynes, TsN3 in presence O2 under mild conditions successfully been developed. The investigation indicated that molecular oxygen (O2) TsN3, respectively, serving as nitrogen sources, were essential successful completion system.

Язык: Английский

Процитировано

2