Electrochemical Selenized Reaction of N-Arylbicyclo[1.1.0]butane-1-carboxamides: Access to 3-(Arylselanyl)spiro[cyclobutane-1,3′-indolin]-2′-one Derivatives DOI

Jiyao Liu,

Yuliang Qian,

Hongrong Zhao

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(21), P. 15914 - 15923

Published: Oct. 23, 2024

A novel selenized reaction of N-arylbicyclo [1.1.0]butane-1-carboxamides with diselenide for the synthesis polycyclic indoline derivatives is developed under electrochemical conditions. The achieved by bicyclo[1.1.0]butane strain-release and intramolecular cyclization process. In addition, this approach features a wide range substrates, good group tolerance, shorter time, mild

Language: Английский

Photocatalytic synthesis of dual acylmethylation derivates of indole[2,1-a]isoquinolinones via tandem cyclization/C3 acyl methylation DOI
Zongbo Xie, Wenli Li, Weiwei Zhang

et al.

Molecular Catalysis, Journal Year: 2025, Volume and Issue: 580, P. 115058 - 115058

Published: April 15, 2025

Language: Английский

Citations

0
Copper(I)-Catalyzed Acylation/Cyclization of 2-Aryl-N-acryloyl Indole toward Indolo[2,1-α]isoquinoline Derivatives DOI

Mengna Yang,

Yucai Tang, Jie Jiang

et al.

Chinese Journal of Organic Chemistry, Journal Year: 2025, Volume and Issue: 45(1), P. 307 - 307

Published: Jan. 1, 2025

Language: Английский

Citations

0
Synthesis of Amide-Containing Indolo[2,1-a]isoquinoline Derivatives via Palladium-Catalyzed Cascade Reactions DOI
Jianyi Ma, Leming Wang, Shufeng Chen

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 8, 2024

A convenient palladium-catalyzed cascade cyclization reaction for the construction of amide-containing indolo[2,1-

Language: Английский

Citations

1
Selenylation/Cyclization of 1‐(2‐(Allyloxy)aryl)‐1H‐indoles Access to Seleno‐Benzo[2,3][1,4]oxazepino[4,5‐a]indole Derivatives DOI Open Access

Hailin Liao,

Mei Pan,

Hongrong Zhao

et al.

Advanced Synthesis & Catalysis, Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 17, 2024

Abstract The iron (ІІІ)‐promoted tandem cyclization of 1‐(2‐(allyloxy)aryl)‐1 H ‐indoles with diselenides has been developed for the preparation seleno‐benzo[2,3][1,4]oxazepino[4,5‐a]indole derivatives. investigation to determine best reaction conditions indicated use (0.2 mmol) (1.5 equiv.) and iron(III) chloride in acetonitrile at room temperature under air, more than 48 examples were obtained. features access selenized 7‐membered containing nitrogen‐oxygen heterocyclic skeleton, which also represents a 7‐exo‐trig process 1‐(2‐((2‐methylallyl)oxy)aryl)‐1 diselenides.

Language: Английский

Citations

0
Electrochemical Selenized Reaction of N-Arylbicyclo[1.1.0]butane-1-carboxamides: Access to 3-(Arylselanyl)spiro[cyclobutane-1,3′-indolin]-2′-one Derivatives DOI

Jiyao Liu,

Yuliang Qian,

Hongrong Zhao

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(21), P. 15914 - 15923

Published: Oct. 23, 2024

A novel selenized reaction of N-arylbicyclo [1.1.0]butane-1-carboxamides with diselenide for the synthesis polycyclic indoline derivatives is developed under electrochemical conditions. The achieved by bicyclo[1.1.0]butane strain-release and intramolecular cyclization process. In addition, this approach features a wide range substrates, good group tolerance, shorter time, mild

Language: Английский

Citations

0