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

Citation
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
Citations number
22
Categorie Soggetti
Food Science & Tenology",Agriculture,"Chemistry Applied
ISSN journal
00218561
Volume
45
Issue
6
Year of publication
1997
Pages
2278 - 2283
Database
ISI
SICI code
0021-8561(1997)45:6<2278:AOASOT>2.0.ZU;2-O
Abstract
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.