Strigol and sorgolactone belong to the class of “strigolactones”, which are highly potent germination stimulants of seeds of the parasitic weeds Striga and Orobanche . The aim of the present work was to synthesize all four stereoisomers of demethylsorgolactone ( 6 ), which lacks the methyl group in the A-ring of naturally occurring sorgolactone, and to evaluate their activities in the stimulation of germination of Striga hermonthica and Orobanche crenata seeds. Two diastereomers of demethylsorgolactone ( 6 ) were prepared and resolved in the corresponding enantiomers. Bioassays revealed that the germination stimulatory activity of 6 is comparable to that of strigol and that there exist significant differences in activity among the individual stereoisomers.
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Thuring et al. (1997) studied this question.
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