Synthesis and antiproliferative activity of 6,7-aryl/hetaryl coumarins

Two different series of novel analogs of 6,7-aryl/hetaryl coumarins 4 a–4h and 8i–8l have been synthesized by using Suzuki–Miyara cross coupling reaction from 4-methyl-2-oxo-2 H -chromen-7-yl trifluoro-methanesulfonate and 4-methyl-2-oxo-2 H -chromen-6-yl trifluoromethanesulfonate in high yields (70...

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Veröffentlicht in:Russian journal of general chemistry 2016, Vol.86 (1), p.184-189
Hauptverfasser: Jayaprakash Rao, Y., Yadaiah goud, E., Hemasri, Y., Jain, Nishant, Gabriella, Srujana
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Sprache:eng
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Zusammenfassung:Two different series of novel analogs of 6,7-aryl/hetaryl coumarins 4 a–4h and 8i–8l have been synthesized by using Suzuki–Miyara cross coupling reaction from 4-methyl-2-oxo-2 H -chromen-7-yl trifluoro-methanesulfonate and 4-methyl-2-oxo-2 H -chromen-6-yl trifluoromethanesulfonate in high yields (70–90%). All synthesized compounds were elucidated by means of IR, 1 H NMR, 13 C NMR, and MS spectra. The synthesized compounds were tested for antiproliferative activity against different human cancer cell lines (SiHa, MDAMB-231, and PANC-1) and some of products demonstrated the distinctive effect.
ISSN:1070-3632
1608-3350
DOI:10.1134/S1070363216010291