ChemInform Abstract: Ligand‐Enabled Stereoselective β‐C(sp3)—H Fluorination: Synthesis of Unnatural Enantiopure anti‐β‐Fluoro‐α‐amino Acids.

• DOI: 10.1002/chin.201547039
• Publication Date: 2015-11-10T09:42:08Z
• Authors: Ru‐Yi Zhu; Keita Tanaka; Gen‐Cheng Li; Jian He; Hai‐Yan Fu; Su‐Hua Li; Jin‐Quan Yu
• Keywords: Enantiopure drug

Abstract The fluorination is performed on α‐amino acid derivatives carrying a broad range of β‐substituents such as aryl, hetaryl, alkyl, and alkynyl groups endowed with various functional groups.