Synthesis of α-amino-1,3-dicarbonyl compounds via Ugi flow chemistry reaction: access to functionalized 1,2,3-triazoles

被引:0
作者
Vasconcelos, Stanley N. S. [1 ]
Fornari, Evelin [1 ]
Caracelli, Ignez [2 ]
Stefani, Helio A. [1 ]
机构
[1] Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Farm, Sao Paulo, SP, Brazil
[2] Univ Fed Sao Carlos, Dept Fis, Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Multicomponent reaction; MRC; Ugi reaction; Click chemistry; Triazole; Flow chemistry; MULTICOMPONENT REACTIONS; ORGANIC-SYNTHESIS; (-)-LEMONOMYCIN; PEPTOIDS; ACIDS;
D O I
10.1007/s11030-017-9764-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Ugi multicomponent reaction has been used as an important synthetic route to obtain compounds with potential biological activity. We present the rapid and efficient synthesis of -amino-1,3-dicarbonyl compounds in moderate to good yields via Ugi flow chemistry reactions performed with a continuous flow reactor. Such -amino-1,3-dicarbonyl compounds can act as precursors for the production of -amino acids via hydrolysis of the ethyl ester group as well as building blocks for the synthesis of novel compounds with the 1,2,3-triazole ring. The -amino acid derivatives of the Ugi flow chemistry reaction products were then used for dipeptide synthesis.
引用
收藏
页码:893 / 902
页数:10
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