ASYMMETRIC-SYNTHESIS OF ALL STEREOISOMERS OF THE STRIGOL-ANALOG-GR24 - DEPENDENCE OF ABSOLUTE-CONFIGURATION ON STIMULATORY ACTIVITY OF STRIGA-HERMONTHICA AND OROBANCHE-CRENATA SEED-GERMINATION
Jwjf. Thuring et al., ASYMMETRIC-SYNTHESIS OF ALL STEREOISOMERS OF THE STRIGOL-ANALOG-GR24 - DEPENDENCE OF ABSOLUTE-CONFIGURATION ON STIMULATORY ACTIVITY OF STRIGA-HERMONTHICA AND OROBANCHE-CRENATA SEED-GERMINATION, Journal of agricultural and food chemistry, 45(6), 1997, pp. 2278-2283
All four optically pure stereoisomers of the strigol analogue GR24 wer
e prepared via two different routes. In the first approach enantiopure
ABC-fragments 4 were used as the chiral source, whereas in the altern
ative route both antipodes of the latent D-ring 6 were employed. Bioas
says revealed significant differences in activity between the four ste
reoisomers in the stimulation of germination of the parasitic weeds St
riga hermonthica and Orobanche crenata.