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Expeditious and scalable preparation of a Li-Thiele reagent for amine-based bioconjugation
Authors:Jiacheng Li  Yuyong Ma  Xiang Zhang  Xin Cao  Hegui Gong  Ang Li
Affiliation:1. Department of Chemistry, Shanghai University, Shanghai 200444, China;2. State Key Laboratory of Bioorganic and Natural Products Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai 200032, China
Abstract:Chemoselective amine bioco njugation has long been a challenge for native protein modification.Inspired by Thiele's seminal discovery,Li and co-workers recently developed an orto-phthalaldehyde(OPA)based reagent for labeling the amino group of a protein.Here we report an expeditious and scalable synthesis of a Li-Thiele reagent featuring an arene construction strategy.The reagent contains an alkyne side chain as a handle for secondary modification.
Keywords:Amine-based bioconjugation  Li?Thiele reagent  Arene synthesis
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