Regioselective syn-1,2-Hydroarylation of Internal Alkynes DOI
Shubham Dutta, M. K. Sethi, Avijit Maity

et al.

Organic Chemistry Frontiers, Journal Year: 2024, Volume and Issue: 11(24), P. 7168 - 7175

Published: Jan. 1, 2024

The regioselective hydro-functionalization reaction is a powerful method to convert readily available alkynes into structurally diverse olefins.

Language: Английский

Near-Infrared-Light-Induced Iron(I) Dimer Enabled Abstraction of Ester Group from Cycloketone Oxime Esters DOI
Xiao-Di Su, Xuening Li, Qiang Liu

et al.

Organic Letters, Journal Year: 2025, Volume and Issue: unknown

Published: March 20, 2025

Photoinduced dimeric metal complexes have been extensively utilized in halogen atom transfer (XAT) reactions. In this study, we successfully achieved the abstraction of ester group from cyclobutanone oxime esters via iron(I)-dimer catalysis under near-infrared (NIR) light (730 nm) excitation, enabling efficient synthesis cyanoalkylated alkenes, quinazolinones, and 3,3-disubstituted oxindoles. Mechanistic investigations confirmed NIR-induced functional process.

Language: Английский

Citations

0

Regioselective syn-1,2-Hydroarylation of Internal Alkynes DOI
Shubham Dutta, M. K. Sethi, Avijit Maity

et al.

Organic Chemistry Frontiers, Journal Year: 2024, Volume and Issue: 11(24), P. 7168 - 7175

Published: Jan. 1, 2024

The regioselective hydro-functionalization reaction is a powerful method to convert readily available alkynes into structurally diverse olefins.

Language: Английский

Citations

1