Skeletal Reorganization Emanated via the Course of Heterocyclic N1–N2 Bond Cleavage: Electrosynthetic Approach DOI
Saiful Islam, Dwaipayan Das,

Rahul Dev Mandal

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(21), P. 15686 - 15693

Published: Oct. 21, 2024

A unified method toward the synthesis of functionalized diazepines and quinazolines through reorganization molecular skeleton has been devised. The process is indulged by electrical energy via a domino N1–N2 bond cleavage followed concomitant ring closing, initiating from cinnolines indazoles as designed precursors. Additionally, an intermolecular homologation also established to synthesize densely dihydroquinazolines 2,3-diaryl-indazoles acetonitrile involving same electrochemical strategy.

Language: Английский

Electrochemically Promoted Transesterification Reaction of Glycine Derivatives DOI
Xiaohu You,

Kejin Huang,

Shi‐Yi Zhuang

et al.

Chinese Journal of Organic Chemistry, Journal Year: 2025, Volume and Issue: 45(4), P. 1360 - 1360

Published: Jan. 1, 2025

Language: Английский

Citations

0
Visible-Light-Triggered Radical-Addition/Ring-Opening Cascade Reactions of 2H-Indazoles to Access ortho-Alkoxycarbonylated Azobenzenes DOI
Zhenhua Li,

Longfeng Yuan,

Yingyan Cao

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(20), P. 14802 - 14810

Published: Oct. 8, 2024

A series of asymmetric azobenzenes have been synthesized by radical-addition/ring-opening cascade reactions from 2

Language: Английский

Citations

0
Skeletal Reorganization Emanated via the Course of Heterocyclic N1–N2 Bond Cleavage: Electrosynthetic Approach DOI
Saiful Islam, Dwaipayan Das,

Rahul Dev Mandal

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(21), P. 15686 - 15693

Published: Oct. 21, 2024

A unified method toward the synthesis of functionalized diazepines and quinazolines through reorganization molecular skeleton has been devised. The process is indulged by electrical energy via a domino N1–N2 bond cleavage followed concomitant ring closing, initiating from cinnolines indazoles as designed precursors. Additionally, an intermolecular homologation also established to synthesize densely dihydroquinazolines 2,3-diaryl-indazoles acetonitrile involving same electrochemical strategy.

Language: Английский

Citations

0