Chiral Acylation with N-(Protected α-Aminoacyl)benzotriazoles for Advantageous Syntheses of Peptides and Peptide Conjugates

被引:50
作者
Katritzky, Alan R. [1 ]
Angrish, Parul [1 ]
Todadze, Ekaterina [1 ]
机构
[1] Univ Florida, Dept Chem, Ctr Heterocycl Cpds, Gainesville, FL 32611 USA
关键词
N-(alpha-aminoacyl)benzotriazoles; N-aminoacylation; O-aminoacylation; peptides; peptoids; SOLID-PHASE SYNTHESIS; CONVENIENT BUILDING-BLOCKS; HIGHLY EFFICIENT SYNTHESIS; UNPROTECTED AMINO-ACIDS; AZA-STEROIDAL ESTER; COUPLING REAGENTS; MONOSACCHARIDE ESTERS; CARBOXYLIC-ACIDS; CHAIN EXTENSION; BOND FORMATION;
D O I
10.1055/s-0029-1217827
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
N-(Protected alpha-aminoacyl)benzotriazoles are efficient intermediates for N- and O-aminoacylation. These intermediates enable fast preparations of biologically relevant peptides and peptide conjugates in high yields and purity, under mild reaction conditions, with full retention of the original chirality. The developed methodology allows simple solution- and solid-phase preparative techniques to generate complex peptides and peptide conjugates and serves as a platform for generating diverse medicinal chemistry building block libraries involving amino acid and heterocyclic moieties crucial for drug development.
引用
收藏
页码:2392 / 2411
页数:20
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