Progress in heterocyclic chemistry, Journal Year: 2024, Volume and Issue: unknown, P. 309 - 354
Published: Jan. 1, 2024
Language: Английский
RSC Advances, Journal Year: 2024, Volume and Issue: 14(29), P. 21047 - 21064
Published: Jan. 1, 2024
Synthesis of quinoid heteroaryls via gold-catalyzed cascade protocols: recent advances and methodologies.
Language: Английский
Citations
8
The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(11), P. 7446 - 7454
Published: May 15, 2024
A copper(I)-catalyzed protocol is developed for the synthesis of various 2,3-diaroylquinolines starting from achiral ammonium salts and anthranils through [4+1+1] annulation. Using copper(I) chloride as sole catalyst, this reaction featured with easily available materials, broad substrate scope, good yields simple conditions.
Language: Английский
Citations
3
The Chemical Record, Journal Year: 2025, Volume and Issue: unknown
Published: April 7, 2025
Abstract Gold catalysis has experienced remarkable progress over the past two decades, particularly in transformations involving alkynes. While numerous aspects of gold‐catalyzed reactions have been extensively reviewed, specific area cascade annulations between functionalized amines and alkynes represents a distinct rapidly developing direction that warrants focused attention. This survey collects systematically analyzes these transformations, which emerged as convenient synthetic strategies to diverse nitrogen heterocycles. The relevant are classified firstly by chemical nature amine functional substituent, secondly size formed ring. field under consideration bridges several fundamental practical branches chemistry, including catalysis, organic synthesis, medicinal materials science.
Language: Английский
Citations
0
The Journal of Organic Chemistry, Journal Year: 2025, Volume and Issue: unknown
Published: May 6, 2025
A novel electrochemical procedure for the one-pot synthesis of variously substituted 5-thiotetrazole has been established by a three-component reaction (thiol(thiophenol)s, isocyanides, and azidotrimethylsilane). This approach is achieved sulfidation isocyanide subsequent cycloaddition with azidotrimethylsilane under mild conditions without metal catalyst or external oxidant. Importantly, presented methodology not only features wide substrate scope but also exhibits practicality showcased gram-scale various conversions.
Language: Английский
Citations
0
Advanced Synthesis & Catalysis, Journal Year: 2024, Volume and Issue: 366(19), P. 4139 - 4144
Published: July 2, 2024
Abstract A copper‐catalyzed annulation of enaminones with maleimides was developed to synthesize various pyrrolo[3,4‐e]isoindoles. In this strategy, 2‐aminopyridine served as a traceless directing group, and target products were obtained in 54–72% yields. Moreover, plausible mechanism for reaction proposed based on several control experiments, deuterium exchange previous reports.
Language: Английский
Citations
3
Green Chemistry, Journal Year: 2024, Volume and Issue: 26(17), P. 9295 - 9299
Published: Jan. 1, 2024
A concise and efficient protocol for the synthesis of various 2-alkenylindole derivatives is developed through [4 + 1] annulation starting from aminobenzyl phosphonium salts cinnamaldehydes.
Language: Английский
Citations
2
Catalysis Science & Technology, Journal Year: 2024, Volume and Issue: 14(19), P. 5671 - 5677
Published: Jan. 1, 2024
Coinage (Au, Ag, Cu) metal-catalyzed (3 + 2) annulation of α-aminoketones and electron-deficient alkynes provides a modular one-step route to variety 3-EWG-substituted pyrroles.
Language: Английский
Citations
2
Progress in heterocyclic chemistry, Journal Year: 2024, Volume and Issue: unknown, P. 309 - 354
Published: Jan. 1, 2024
Language: Английский
Citations
0