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Triflic Anhydride Promoted Decarboxylative Functionalization of α-Amino Acids

2025-10-16 by admin

Mingyue Yuan, Mingliang Lou, Gen Li and Xiangbing Qi

The decarboxylation of naturally abundant amino acids, followed by subsequent inter- or intramolecular reaction cascades, enables the rapid synthesis of a variety of diverse and high-value amine derivatives. Previous methods have relied heavily on transition metals, involved tedious procedures, or required harsh conditions. Herein, we present a novel reaction cascade for the decarboxylation and nucleophilic functionalization of α-amino acids. This method is characterized by being transition-metal-free, convenient to operate, environmentally friendly and having mild conditions.

DOI: 10.1021/acs.orglett.4c02589

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Enantioselective Decarboxylative C(sp3)-C(sp3) Cross-Coupling of Aliphatic Redox-Active Esters with gem-Borazirconocene Alkanes

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