| Asymmetric Synthesis of α, α′-Disubstituted α-Amino Acids Based on Natural (1R)-( + )-Camphor |
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| 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 |
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| 作者姓名： | LI Shuo LI Lei XU Peng-Fei |
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| 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） |
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| 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]
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Asymmetric Synthesis of α, α′-Disubstituted α-Amino Acids Based on Natural (1R)-( + )-Camphor |
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| 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 |
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| Authors: | Li Shuo LI Lei XU Peng-fei |
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| 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] |
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