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

Vasconcelos, Stanley N. S.
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机构:
Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Farm, Sao Paulo, SP, Brazil Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Farm, Sao Paulo, SP, Brazil

Fornari, Evelin
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机构:
Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Farm, Sao Paulo, SP, Brazil Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Farm, Sao Paulo, SP, Brazil

Caracelli, Ignez
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机构:
Univ Fed Sao Carlos, Dept Fis, Sao Carlos, SP, Brazil Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Farm, Sao Paulo, SP, Brazil

Stefani, Helio A.
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机构:
Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Farm, Sao Paulo, SP, Brazil Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Farm, Sao Paulo, SP, Brazil
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.
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页码:893 / 902
页数:10
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