Synthesis and in vitro anti-HIV-1 evaluation of some N-arylsulfonyl-3-formylindoles

Author:

Che Zhiping1,Tian Yuee1,Liu Shengming1,Hu Mei1,Chen Genqiang1

Affiliation:

1. Henan University of Science and Technology, China

Publisher

FapUNIFESP (SciELO)

Reference27 articles.

1. Triflic acid controlled successive annelation of aromatic sulfonamides an efficient one-pot synthesis of N-sulfonyl pyrroles, indoles and carbazoles;Abid M;Tetrahedron Lett,2007

2. Next-generation HIV-1 non-nucleoside reverse transcriptase inhibitors;Boone LR;Curr Opin Investig Drugs,2006

3. Rational design, synthesis, anti-HIV-1 RT and antimicrobial activity of novel 3-(6-methoxy-3,4-dihydroquinolin-1(2H)-yl)-1-(piperazin-1-yl) propan-1-one derivatives;Chander S;Bioorg Chem,2016

4. Microwave-assisted combinatorial synthesis of 2-alkyl-2-(N-arylsulfonylindol-3-yl)-3-N-acyl-5-aryl-1,3,4-oxadiazolines as anti-HIV-1 agents;Che ZP;Comb Chem High T Scr,2013

5. Design and synthesis of novel N-arylsulfonyl-3-(2-yl-ethanone)-6-methylindole derivatives as inhibitors of HIV-1 replication;Che ZP;Pharmaceuticals,2015

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