Asymmetric synthesis of β-hydroxy-α-amino acid

被引:19
|
作者
Makino, K [1 ]
Hamada, Y [1 ]
机构
[1] Chiba Univ, Grad Sch Pharmaceut Sci, Inage Ku, Chiba 2638522, Japan
关键词
beta-hydroxy-alpha-amino acid; asymmetric synthesis; GE; 3; polyoxypeptin; papuamide; dynamic kinetic resolution; asymmetric hydrogenation; beta-hydroxyleucine; ruthenium; BINAP;
D O I
10.5059/yukigoseikyokaishi.63.1198
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
beta-Hydroxy-alpha-amino acids are valuable constituents of complex natural products and medicinally important compounds. For instance, the naturally occurrence beta-hydroxyleucine is a representative of this class and has attracted considerable attention as an unusual amino acid constituent of cyclodepsipeptides such as azinothricin, A 83586 C, papuamides, polyoxypeptins and GE 3. As a consequence of the importance of beta-hydroxy-alpha-amino acids in the biological activities as well as their usefulness as synthetic building blocks, a number of useful strategies have been devised for better method of the synthesis of beta-hydroxy-alpha-amino acids. This review summarizes recent progress in asymmetric synthesis of beta-hydroxy-alpha-amino acids.
引用
收藏
页码:1198 / 1208
页数:11
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