Repositori URV

Identificador: imarina:9322152

Handle: https://hdl.handle.net/20.500.11797/imarina9322152

Autores:
Zuccarello, GNannini, LJArroyo-Bondía, AFincias, NArranz, IPérez-Jimeno, AHPeeters, MMartín-Torres, ISadurní, AGarcía-Vázquez, VWang, YFKirillova, MSMontesinos-Magraner, MCaniparoli, UNúñez, GMaseras, FBesora, MEscofet, IEchavarren, AM

Resumen:
A new generation of chiral gold(I) catalysts based on variations of complexes with JohnPhos-type ligands with a remote C2-symmetric 2,5-diarylpyrrolidine have been synthesized with different substitutions at the top and bottom aryl rings: from replacing the phosphine by a N-heterocyclic carbene (NHC) to increasing the steric hindrance with bis- or tris-biphenylphosphine scaffolds, or by directly attaching the C2-chiral pyrrolidine in the ortho-position of the dialkylphenyl phosphine. The new chiral gold(I) catalysts have been tested in the intramolecular [4+2] cycloaddition of arylalkynes with alkenes and in the atroposelective synthesis of 2-arylindoles. Interestingly, simpler catalysts with the C2-chiral pyrrolidine in the ortho-position of the dialkylphenyl phosphine led to the formation of opposite enantiomers. The chiral binding pockets of the new catalysts have been analyzed by DFT calculations. As revealed by non-covalent interaction plots, attractive non-covalent interactions between substrates and catalysts direct specific enantioselective folding. Furthermore, we have introduced the open-source tool NEST, specifically designed to account for steric effects in cylindrical-shaped complexes, which allows predicting experimental enantioselectivities in our systems.© 2023 The Authors. Published by American Chemical Society.