2017
DOI: 10.1016/j.jplph.2017.04.021
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Synthesis of tricyclic butenolides and comparison their effects with known smoke—butenolide, KAR1

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Cited by 6 publications
(2 citation statements)
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“…50 analogs (Nelson et al 2012). In one of the studies (Krawczyk et al 2017), tricyclic butenolides (KAR 1 with an additional aromatic ring or an aromatic ring without the methyl group at the C3 position of karrikin) were applied to dormant and non-dormant A. fatua caryopses. A low stimulatory effect on germination of dormant caryopses was shown only by those butenolides without the methyl group.…”
Section: Tricyclic Butenolidesmentioning
confidence: 99%
“…50 analogs (Nelson et al 2012). In one of the studies (Krawczyk et al 2017), tricyclic butenolides (KAR 1 with an additional aromatic ring or an aromatic ring without the methyl group at the C3 position of karrikin) were applied to dormant and non-dormant A. fatua caryopses. A low stimulatory effect on germination of dormant caryopses was shown only by those butenolides without the methyl group.…”
Section: Tricyclic Butenolidesmentioning
confidence: 99%
“…Smoke generating from burning plant material has been known to contain karrikins (KAR 1 )—chemicals that are powerful germination promoters. KAR 1 plays a major role in natural systems as it is highly active at very low concentrations, shows great potential in agriculture [1] and is promising to be a new plant growth regulator [2,3,4,5,6,7,8]. Until now the effects and potential mechanisms of KAR 1 on the accumulation of secondary metabolite in medicinal plants has not been reported.…”
Section: Introductionmentioning
confidence: 99%