Green One-Pot Asymmetric Synthesis of Peptidomimetics via Sequential Organocatalyzed Aziridination and Passerini Multicomponent Reaction

被引:4
|
作者
dos Santos, Deborah A. [1 ,2 ]
da Silva, Allan R. [1 ,2 ]
Ellena, Javier [3 ]
da Silva, Cecilia C. P. [2 ]
Paixao, Marcio W. [1 ,2 ]
Correa, Arlene G. [1 ,2 ]
机构
[1] Univ Fed Sao Carlos, Ctr Excellence Res Sustainable Chem, BR-13565905 Sao Carlos, SP, Brazil
[2] Univ Fed Sao Carlos, Dept Chem, BR-13565905 Sao Carlos, SP, Brazil
[3] Univ Sao Paulo, Sao Carlos Inst Phys, BR-13560570 Sao Carlos, SP, Brazil
来源
SYNTHESIS-STUTTGART | 2020年 / 52卷 / 07期
关键词
peptidomimetics; green chemistry; organocatalysis; aziridine; multicomponent reaction; ENANTIOSELECTIVE AZIRIDINATION;
D O I
10.1055/s-0039-1690774
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Peptidomimetics containing an aziridine moiety have been reported as potent cysteine protease inhibitors. In this sense, the development of stereoselective and sustainable synthetic strategies to obtain three-membered N -heterocyclic compounds has gained importance in the last decades. In this work, an efficient method was designed to achieve highly functionalized aziridine peptidomimetics via a sequential reaction, which involves the organocatalytic aziridination of alpha,beta-unsaturated aldehydes followed by the Passerini multicomponent reaction in an environmentally friendly solvent mixture (ethanol: water).
引用
收藏
页码:1076 / 1086
页数:11
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