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Asymmetric Synthesis of α, α′-Disubstituted α-Amino Acids Based on Natural (1R)-( + )-Camphor
引用本文:LI Shuo,LI Lei,XU Peng-Fei.Asymmetric Synthesis of α, α′-Disubstituted α-Amino Acids Based on Natural (1R)-( + )-Camphor[J].有机化学,2003,23(Z1):419-419.
作者姓名:LI Shuo  LI Lei  XU Peng-Fei
作者单位:LI Shuo(State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000)  LI Lei(State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000)  XU Peng-Fei(State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000)
摘    要:Optically active nonproteinogenic amino acids 1] are valuable compounds of high interest not only owing to their remarkable pharmacological and biological activities, but also for their role as an investigative topographic probe for bioactive conformations of peptides and the mechanisms of enzyme reactions.2]


Asymmetric Synthesis of α, α′-Disubstituted α-Amino Acids Based on Natural (1R)-( + )-Camphor
Li Shuo,LI Lei,XU Peng-fei.Asymmetric Synthesis of α, α′-Disubstituted α-Amino Acids Based on Natural (1R)-( + )-Camphor[J].Chinese Journal of Organic Chemistry,2003,23(Z1):419-419.
Authors:Li Shuo  LI Lei  XU Peng-fei
Abstract:Optically active nonproteinogenic amino acids 1] are valuable compounds of high interest not only owing to their remarkable pharmacological and biological activities, but also for their role as an investigative topographic probe for bioactive conformations of peptides and the mechanisms of enzyme reactions.2]
Keywords:
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