Abstract
New isocoumarins were prepared in an efficient way from 2-iodobenzoic acid derivatives and hept-1-yne in a Sonogashira reaction, followed by spontaneous cyclization. Catalytic hydrogenation gave the corresponding dihydroisocoumarins. A 4-chloroisocoumarin was prepared on an alternative pathway. Some of the new compounds showed moderate cytotoxic activities against a human leukemia cell line (HL 60). © Hampl et al.
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Hampl, V., Wetzel, I., Bracher, F., & Krauss, J. (2011). New Substituted isocoumarins and dihydroisocoumarins and their cytotoxic activities. Scientia Pharmaceutica, 79(1), 21–30. https://doi.org/10.3797/scipharm.1011-10
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