Micelle-Assisted C(sp2)–H Functionalization for C–Se and C–X Bond Formation in the Aqueous Medium DOI

Abhinay S. Chillal,

Chandra B Maurya,

Umesh A. Kshirsagar

et al.

Langmuir, Journal Year: 2024, Volume and Issue: 40(44), P. 23445 - 23457

Published: Oct. 21, 2024

An environmentally sustainable, versatile, and cost-effective approach for C-Se C-X (X = I, Br, Cl) bond formation through C-H functionalization assisted by micellar catalysis in water is developed. The reaction utilizes a minimum amount of diorganyl diselenides potassium halides the respective functionalizations. present protocol was suitable scale-up synthesis, which directly provided desired selenylated products without need chromatographic purification, sufficient purity. aqueous system reusable up to 5 cycles compromising yield.

Language: Английский

Visible-Light-Mediated, Organophotocatalytic C–H Thiocyanation of Pyrazolo[1,5-a]pyrimidines DOI
Paramita Pattanayak,

Appanapalli N. V. Satyanarayana,

Tanmay Chatterjee

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(18), P. 13215 - 13223

Published: Sept. 11, 2024

Herein, we report a metal-free, organophotoredox-catalyzed sustainable C-H thiocyanation of biologically active class N-heterocycles, pyrazolo[1,5-

Language: Английский

Citations

2

Electrochemical Regioselective C(sp2)–H Bond Chalcogenation of Pyrazolo[1,5-a]pyrimidines via Radical Cross-Coupling at Room Temperature DOI

Abhinay S. Chillal,

Rajesh T. Bhawale,

Siddharth Sharma

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(19), P. 14496 - 14504

Published: Sept. 16, 2024

Herein, we disclose an electrochemical approach for the C(sp

Language: Английский

Citations

1

Micelle-Assisted C(sp2)–H Functionalization for C–Se and C–X Bond Formation in the Aqueous Medium DOI

Abhinay S. Chillal,

Chandra B Maurya,

Umesh A. Kshirsagar

et al.

Langmuir, Journal Year: 2024, Volume and Issue: 40(44), P. 23445 - 23457

Published: Oct. 21, 2024

An environmentally sustainable, versatile, and cost-effective approach for C-Se C-X (X = I, Br, Cl) bond formation through C-H functionalization assisted by micellar catalysis in water is developed. The reaction utilizes a minimum amount of diorganyl diselenides potassium halides the respective functionalizations. present protocol was suitable scale-up synthesis, which directly provided desired selenylated products without need chromatographic purification, sufficient purity. aqueous system reusable up to 5 cycles compromising yield.

Language: Английский

Citations

0