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1 3-ol, 6-methyl-5-hepten-2-one, benzaldehyde, methyl salicylate).
2 OR activation by converting acetophenone to methyl salicylate.
3 dly metabolized to SA O-beta-D-glucoside and methyl salicylate.
4 onomer is mainly responsible for protonating methyl salicylate.
5 n air of the chemical warfare agent simulant methyl salicylate (1.24 ppb) and for nitrobenzene (629 p
7 hermolysis (FVT) with Ar-matrix isolation of methyl salicylate (7), 2-phenylbenzo-1,3-dioxan-4-one (8
8 he observed labeling pattern in the isolated methyl salicylate 7a/7b and methyl cyclopentadienecarbox
9 modified electrode was fabricated to detect methyl salicylate, a volatile organic compound released
10 act plants sprayed with methyl jasmonate and methyl salicylate and in excised leaves supplied through
11 c acid (JA) biosynthesis genes and exogenous methyl salicylate and methyl jasmonate applications show
13 given for chemical warfare agent simulants, methyl salicylate, and dimethyl methyl phosphonate (DMMP
15 s of salicylaldehyde, o-hydroxyacetophenone, methyl salicylate, and methyl N-methyl- or N-phenylanthr
16 on of the alpha-chlorophenylacetate ester of methyl salicylate as demonstrated by a trapping experime
18 that SABP2 has strong esterase activity with methyl salicylate as the substrate, and that SA is a pot
20 l sulfoxide (DMSO), dimethylformamide (DMF), methyl salicylate, caffeine, l-leucine, l-histidine, lor
21 rmone analogues such as methyl jasmonate and methyl salicylate can trigger defense responses in plant
23 ylate (43.30%) and a significant decrease in methyl salicylate content in spring bamboo shoots were o
25 peas and a plant-derived repellent compound, methyl salicylate, differed between morphs or sexes.
28 nd 2, the approach was first to react either methyl salicylate (for 1) or phenyl salicylate (for 2) w
32 critical for methyl salicylate synthesis and methyl salicylate, in turn, likely has an important role
33 ormance of the technique is established with methyl salicylate, including a limit of quantification o
34 tive but mounted normal local resistance and methyl salicylate-induced defense responses, suggesting
36 production of plant volatiles, particularly methyl salicylate, making bean plants, Vicia faba, repel
37 idual components elicited varying responses; Methyl salicylate (MeSA) elicited the highest positive c
38 cquired resistance (SAR) in tobacco; SABP2's methyl salicylate (MeSA) esterase activity is required i
39 rent genetic backgrounds, we showed that the methyl salicylate (MeSA) esterase activity of salicylic
44 O2* with five GLVs: methyl jasmonate (MeJa), methyl salicylate (MeSa), cis-3-hexenyl acetate (HxAc),
45 ajor aphid-induced VOCs (ethanone, limonene, methyl salicylate, myrcene, ocimene) triggered resistanc
46 s not induced by wounding, methyl jasmonate, methyl salicylate, or ethephon, synthetic GmSubPep pepti
48 results indicate that SlSAMT is critical for methyl salicylate synthesis and methyl salicylate, in tu
50 mall metabolites in SAR signaling, including methyl salicylate, the abietane diterpenoid dehydroabiet
52 peciosa recruit to aboveground herbivory and methyl salicylate treatment, that larval D. speciosa are
55 , beta-ionone, hotrienol, methylpyrazine and methyl salicylate were major volatile constituents in al
56 hoots at ambient temperature comprise 12.30% methyl salicylate, which provides protection against ins
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