An efficient method for the preparation of peptide alcohols

被引:13
作者
Katritzky, Alan Roy [1 ]
Abo-Dya, Nader Elmaghwry [1 ,2 ]
Tala, Srinivasa Rao [1 ]
Gyanda, Kapil [1 ]
Abdel-Samii, Zakaria Kamel [2 ]
机构
[1] Univ Florida, Dept Chem, Ctr Heterocycl Cpds, Gainesville, FL 32611 USA
[2] Zagazig Univ, Fac Pharm, Dept Organ Pharmaceut Chem, Zagazig 44519, Egypt
关键词
ASYMMETRIC TRANSFER-HYDROGENATION; AMINO-ACIDS; ALDEHYDES; CONVENIENT; DIPEPTIDES; LIGANDS; FMOC-ALPHA-AMINOACYL)BENZOTRIAZOLES; DERIVATIVES; REDUCTION; ACYLATION;
D O I
10.1039/b905730g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
N-Protected LL-dipeptide alcohols 3a-p, diastereomeric mixture (3d + 3d') and tripeptide alcohols 6a-c were synthesized by treatment of various amino alcohols with N-protected(alpha-aminoacyl)benzotriazoles 1a-c, 1f-m, (1a + 1a') and N-protected(alpha-dipeptidoyl) benzotriazoles 5a, 5b respectively in good yields with complete retention of chirality.
引用
收藏
页码:4444 / 4447
页数:4
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