General and efficient synthesis of benzoxazol-2(3H)-ones: evolution of their anti-cancer and anti-mycobacterial activities
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A novel class of benzo[d]oxazol-2(3H)-one derivatives has been synthesized and their in vitro cytotoxicity against human pancreatic adenocarcinoma and human non-small cell lung carcinoma cancer cell lines was evaluated.
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1994 ◽
Vol 30
(1)
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pp. 97-102
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1998 ◽
Vol 34
(5)
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pp. 724-730
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2012 ◽
Vol 35
(7)
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pp. 1251-1258
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1985 ◽
Vol 75
(1)
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pp. 306-309
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