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Site-selective and diastereoselective functionalization of α-amino acid and peptide derivatives via palladium-catalyzed sp3 C–H activation
Ming Zhang,Shengliang Zhong,Yiyuan Peng,Jianwen Jiang,Yongli Zhao,Changfeng Wan,Zhenming Zhang,Rongli Zhang,Ai Qin Zhang
Organic Chemistry Frontiers Pub Date : 10/26/2020 00:00:00 , DOI:10.1039/D0QO00988A
Abstract

α-Amino acid and peptide derivatives are important in synthetic organic chemistry and medicinal chemistry, which attract many chemists to develop new methods for their synthesis. Palladium-catalyzed sp3 C–H activation/functionalization has been developed greatly for the modification of α-amino acids and peptides. This review introduces palladium-catalyzed sp3 C–H activation/functionalization of amino acids and peptides. The content includes intermolecular functionalization (arylation, alkylation, alkenylation, alkynylation, acetoxylation, fluorination, silylation, borylation, sulfonylation, chalcogenation and carbonylative cyclization) and intramolecular functionalization (intramolecular C–N bond-forming cyclization and peptide macrocyclization).

Graphical abstract: Site-selective and diastereoselective functionalization of α-amino acid and peptide derivatives via palladium-catalyzed sp3 C–H activation
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