1,2,3-Triazole derivatives of 3-ferrocenylidene-2-oxindole: Synthesis, characterization, electrochemical and antimicrobial evaluation

被引:18
|
作者
Yagnam, Swetha [1 ,5 ]
Reddy, Eda Rami [1 ]
Trivedi, Rajiv [1 ,5 ]
Krishna, Narra Vamshi [2 ]
Giribabu, Lingamallu [2 ,5 ]
Rathod, Balaji [3 ]
Prakasham, Reddy Shetty [3 ,5 ]
Sridhar, Balasubramanian [4 ,5 ]
机构
[1] Indian Inst Chem Technol, CSIR, Catalysis & Fine Chem Div, Uppal Rd, Hyderabad 500007, Telangana, India
[2] Indian Inst Chem Technol, CSIR, Polymer & Funct Mat Div, Hyderabad 500007, Telangana, India
[3] Indian Inst Chem Technol, CSIR, Organ Synth & Proc Chem, Hyderabad 500007, Telangana, India
[4] Indian Inst Chem Technol, CSIR, Ctr Xray Crystallog, Hyderabad 500007, Telangana, India
[5] CSIR, AcSIR, Acad Sci & Innovat Res, IICT Campus, Hyderabad 500007, Telangana, India
关键词
antimicrobial activity; aryl; benzyl; electrochemistry; ferrocene-conjugated oxindole; sugar and aliphatic azides; triazoles; CLICK CHEMISTRY; ANTIMALARIAL ACTIVITY; BIOLOGICAL-ACTIVITY; IN-VITRO; FERROCENE; CANCER; CHLOROQUINE; FERROQUINE; TRIAZOLES; SERIES;
D O I
10.1002/aoc.4817
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A series of bioactive, triazole-linked benzyl, aryl, sugar and aliphatic conjugates of 3-ferrocenylidene-oxindole have been synthesized. A facile 1,3-dipolar-Huisgen coupling reaction of the respective azides with the 3-ferrocenylidene-oxindole N-propargyl moiety (3) gave the corresponding conjugates (5a-n). All the newly synthesized compounds (5a-n) were characterized by H-1-NMR, C-13-NMR, HRMS, Fourier transform-infrared spectroscopy and elemental analysis. The UV-Vis and electrochemical studies of these compounds were performed in dimethylsulfoxide solutions. The structure of compound (3) was determined by single crystal X-ray diffraction study. These compounds exhibited moderate to good antimicrobial activity against Gram-positive and Gram-negative strains.
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页数:15
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