ACS Catalysis, Journal Year: 2024, Volume and Issue: unknown, P. 16639 - 16648
Published: Oct. 28, 2024
Language: Английский
ACS Catalysis, Journal Year: 2024, Volume and Issue: unknown, P. 16639 - 16648
Published: Oct. 28, 2024
Language: Английский
Organic Letters, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 9, 2025
Transition-metal-catalyzed [2 + 2 2] annulation of alkynes is an efficient pathway for the synthesis aromatic compounds. However, most established methods require noble metal catalysts. Herein, we report a copper-catalyzed intermolecular diynes with through vinyl cation intermediates, enabling atom-economical preparation biologically important carbazole skeletons. The reaction shows good regioselectivity in aryl(alkyl)alkynes. Moreover, preliminary results have also been obtained related catalytic atroposelective transformation. This represents rare example non-noble-metal-catalyzed ynamides pathway.
Language: Английский
Citations
1ACS Catalysis, Journal Year: 2025, Volume and Issue: unknown, P. 2939 - 2949
Published: Feb. 4, 2025
Language: Английский
Citations
1Organic Letters, Journal Year: 2024, Volume and Issue: 26(31), P. 6586 - 6590
Published: July 30, 2024
A rhodium-catalyzed [4 + 2] cycloaddition of ynamines and 2-(cyanomethyl)phenylboronates has been developed, leading to efficient excellent regioselective synthesis valuable indole-linked aromatic compounds in a concise flexible approach. Interestingly, this strategy was successful the construction C···N axially chiral indoles with high enantiocontrol by introduction new phosphoramidite ligand (Xie-Phos).
Language: Английский
Citations
0ChemCatChem, Journal Year: 2024, Volume and Issue: unknown
Published: Sept. 3, 2024
Abstract Axially chiral indoline‐based scaffolds are virtually universal in biological and pharmaceutical compounds. In this study, we demonstrate the Rh‐catalyzed asymmetric [2 + 2 2] cycloaddition of 1,6‐enynes with steric hindered N‐ alkynyl indoles, which enables simultaneous construction both axial central chirality, containing a quaternary carbon center, one step. Notable features these reactions include excellent chemo‐, regio‐, diastereo‐ enantioselectivity, 100% atom‐economy, easily available SEGPHOS ligand, mild conditions.
Language: Английский
Citations
0ACS Catalysis, Journal Year: 2024, Volume and Issue: unknown, P. 16639 - 16648
Published: Oct. 28, 2024
Language: Английский
Citations
0