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1 carbonyls (phenylacetaldehyde, acrolein, and crotonaldehyde).
2 the mutagenic and carcinogenic properties of crotonaldehyde.
3  useful conversions only with type-II olefin crotonaldehyde.
4 o exclusively yield the C4 coupling product, crotonaldehyde.
5 yl-2-pentylpyridine) produced by 2-alkenals (crotonaldehyde, 2-hexenal, and 2-octenal) in the presenc
6 te the phenomenon for activation pathways of crotonaldehyde, a model a,B-unsaturated aldehyde relevan
7 nethiol, a microbial-human cometabolite, and crotonaldehyde, a product of lipid peroxidation, these f
8 om cigarette smoke and polluted air, such as crotonaldehyde, acrolein, and oxidizing agents such as h
9 rchain cross-link formation by the analogous crotonaldehyde adduct (2b) was evaluated in a 5'-dC-2b s
10 ially incorporated opposite the acrolein and crotonaldehyde adducts, and dTTP incorporation was prefe
11                                              Crotonaldehyde adsorbed to Pt(111) as eta(2) surface int
12                  The reaction of 2-alkenals (crotonaldehyde and 2-pentenal) with hydroquinones (hydro
13 imum around pH 6.5, and on concentrations of crotonaldehyde and creatinine.
14 from the reaction of chlorine with acrolein, crotonaldehyde, and methyl vinyl ketone were tentatively
15  alpha,beta-unsaturated aldehydes, acrolein, crotonaldehyde, and prenal, over Pt(111) at Torr pressur
16 ng adducts derived from butadiene, acrolein, crotonaldehyde, and styrene, and examined for effects on
17 g 1,N(2)-deoxyguanosine adducts of acrolein, crotonaldehyde, and trans-4-hydroxynonenal can form cros
18 ine interstrand cross-links arising from the crotonaldehyde- and acetaldehyde-derived R- and S-alpha-
19 a-unsaturated aldehydes such as acrolein and crotonaldehyde are common environmental pollutants prese
20 se (AOR) from P. furiosus using pyruvate and crotonaldehyde as substrates, respectively.
21 ldehyde by the CM reaction of isoeugenol and crotonaldehyde can be obtained at ambient temperature wi
22        The high reactivity of the isoeugenol/crotonaldehyde combination in olefin metathesis reaction
23 ermidine directly reacts with AA to generate crotonaldehyde (CrA), most likely via an enamine aldol c
24    Activation energy for MeIQ formation from crotonaldehyde, creatinine, and glutamine was 72.2 +/- 0
25 e (dG) with enals, including acrolein (Acr), crotonaldehyde (Cro), pentenal (Pen), heptenal (Hep), an
26                                Acrolein- and crotonaldehyde-derived 1,N2-propanodeoxyguanosine (AdG a
27 cyclic adducts, has shown that acrolein- and crotonaldehyde-derived 1,N2-propanodeoxyguanosine adduct
28                                       Cyclic crotonaldehyde-derived deoxyguanosine (CrA-PdG) adducts
29                     The acrolein- and the 6R-crotonaldehyde-derived exocyclic 1,N(2)-dG adducts form
30              The corresponding acrolein- and crotonaldehyde-derived exocyclic 1,N(2)-dG adducts under
31                      The cinnamaldehyde- and crotonaldehyde-derived phosphonates 2b and 2c were also
32 sitive to acetaldehyde, but not to acrolein, crotonaldehyde, glyoxal, and methylglyoxal.
33           Methacrolein, methyl vinyl ketone, crotonaldehyde, glyoxal, methyl glyoxal, and benzaldehyd
34 aturated carbonyl compounds like acrolein or crotonaldehyde in acetone-d(6) generates metastable (E)-
35 that acrolein was 2000-fold more potent than crotonaldehyde in blocking DNA binding to an NF-kappaB c
36 ld: 16%) and B (1b, overall yield: 34%) from crotonaldehyde in nine and seven steps, respectively, ha
37  We suggest that the superior performance of crotonaldehyde in the CM reactions investigated can be r
38                         The hydrogenation of crotonaldehyde in the presence of supported platinum nan
39                   The repair of acetaldehyde/crotonaldehyde-induced guanine (N2)-guanine (N2) interst
40                        Lastly, we found that crotonaldehyde induces the formation of DNA-Top1 complex
41 d aldehydes in cigarette smoke (acrolein and crotonaldehyde) inhibited production of interleukin-2 (I
42                                              Crotonaldehyde is a representative alpha,beta-unsaturate
43 cy site on the TiO2 surface, the C=O bond of crotonaldehyde is activated, by charge transfer, for hyd
44                           Thus, acetaldehyde/crotonaldehyde mixtures and 2,4-alkadienals were the mai
45 arified by carrying out the hydrogenation of crotonaldehyde over both Pt(111) and Pt(100) single crys
46                                              Crotonaldehyde reacted with Cys-61, but not Arg-307, whe
47 ata to experiments performed with 2-butenal (crotonaldehyde) shows that EpB and 2-butenal decompose t
48  exocyclic 1,N(2)-dG adducts of acrolein and crotonaldehyde, the cross-linking reaction is slow.
49      The 1,4-addition of thioacetic acid and crotonaldehyde to (Z)-3-(acetylsulfanyl)-1-propen-1-ol i
50  that MeIQ was only produced when 2-butenal (crotonaldehyde) was present.
51 oxystyrene with type-II olefins acrolein and crotonaldehyde were investigated in cross-metathesis (CM
52 oduced between the C21:0 alkylresorcinol and crotonaldehyde were isolated and characterized by nuclea
53 ,beta-unsaturated aldehydes (e.g., acrolein, crotonaldehyde) were quantified with a sensitive new ana
54 t a,B-unsaturated carbonyls (e.g., acrolein, crotonaldehyde) will be transformed to an appreciable ex