Published: Jan. 1, 2024
Language: Английский
Published: Jan. 1, 2024
Language: Английский
ACS Catalysis, Journal Year: 2025, Volume and Issue: unknown, P. 5718 - 5730
Published: March 24, 2025
We report the cyclotrimerization reactions of triynes using Mn(I) complexes derived from MnBr(CO)5 and phosphine ligands, such as 1,1-bis(diphenylphosphino)methane (dppm). These are driven by irradiation under mild conditions (30–80 °C) without need additional photoinitiators. Our catalytic screening revealed that counteranions ligands significantly influence process. This method accommodates a broad range functionalities in substrates, including alkyl, aryl, Bpin, SiMe3, GeEt3, PPh2, pyridyl, thienyl moieties, notable interference transformation. Additionally, this enables with oligoalkynes-like (un)substituted hexaynes, producing 2-fold cyclization products very good yields. Under stoichiometric conditions, diynes phosphaalkynes results unique photochemical synthesis phosphinines. Experimental theoretical mechanistic studies indicate dissociation diphosphine ligand precedes involvement Mn carbonyl species cycle. The plays crucial role stabilizing catalyst during transformation preventing formation unreactive cluster species.
Language: Английский
Citations
0Organic Chemistry Frontiers, Journal Year: 2024, Volume and Issue: 11(11), P. 3257 - 3262
Published: Jan. 1, 2024
This work has realized a facile assembly of succinimide-fused 1,3-cyclohexadienes via Co-catalyzed [2 + 2 2] cycloaddition 1,6-diynes to maleimides. Furthermore, the oxidation was carried out under I /MeONa.
Language: Английский
Citations
3ChemCatChem, Journal Year: 2024, Volume and Issue: 16(16)
Published: April 8, 2024
Abstract Cobalt catalysts have recently gained considerable attention as alternatives to based on precious transition metals such Rh and Ir. Recently, Co/photoredox cooperative catalysis has emerged a powerful tool that enables versatile transformations, including cycloaddition reactions of unsaturated compounds. In particular, 1,6‐diyne derivatives are fascinating substrates for these because the corresponding exocyclic 1,3‐diene products can be further transformed into sp 3 ‐rich carbocycles heterocycles via functionalization diene moiety. The dual catalytic system facilitate not only activation π‐bond only, alkyne cyclotrimerization, but also involving σ‐bond activation. This Concept highlights recent advances in cooperative‐catalysis‐enabled reactions, focusing substrates, which difficult perform when well‐defined cationic Co I is employed.
Language: Английский
Citations
1Published: Jan. 1, 2024
Language: Английский
Citations
0