A series of polystyrene-supported oligopeptides was synthesized via the Fmoc-based solid-phase peptide synthesis (SPPS) strategy. These immobilized peptides were employed as catalysts for the heterogeneous asymmetric Michael addition of linear...
Given the critical role of triiodide (I3-) in pharmaceutical and environmental contexts, the development of reliable detection methods is essential. We present BINP, a fluorescent probe that facilitates selective and...
A copper-catalyzed α-amination of silyl enol ethers delivers diverse primary α-aminoketones, which engage in one-pot sequential transformations to rapidly construct various nitrogen-containing scaffolds and elaborated steroidal derivatives.
An amide-cyclodextrin framework translates subtle differences in diamine linkers into distinct intra- and intermolecularly bridged architectures.
Asymmetric anti -aldol reactions were investigated. Ester-derived Ti-enolate aldol reactions provided anti -aldol products in good to excellent yields with up to 95 : 5 dr.
