“…The analogous (1E,4E)-1,5-bis(4-hydroxyphenyl)penta-1,4-dien-3-one and (1E,4E)-1-(2-hydroxyphenyl)-5-phenylpenta-1,4-dien-3-one, on the other hand, have been found to exhibit significant larvicidal activity against mosquito Aedes aegypti (L), [8] a known vector in the transmission of yellow fever, dengue haemorrhagic fever, and the re-emerging disease chikungunya. These compounds have also been found to inhibit binding of cholesterol to Aedes aegypti SCP-2 (AeSCP-2) in vitro [9]. Todate, the structures of the 1,1′-distyryl ketones have only been fully characterised using 1 H-NMR, 13 C-NMR, IR and UV spectrometric techniques and their trans stereochemistry was assigned based on the coupling constant values, J trans = 15.0-16.5 Hz [10].…”