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1 ropofol, an intravenous, strongly lipophilic-substituted phenol.
2 rotein family catalyze the oxidation of para-substituted phenols.
3 ues is achieved from readily available ortho-substituted phenols.
4 of VAO and related enzymes that oxidize para-substituted phenols.
5 e Grignard addition so as to generate highly substituted phenols.
6 r products; syringol, guaiacol, phenols, and substituted phenols.
7 these surface bound species by reaction with substituted phenols.
8 ohexadienone for the construction of m-enone-substituted phenols.
9 enols (2,6-dimethyl- and 2,6-di-tert-butyl-4-substituted phenols, 2,2,5,7,8-pentamethylchroman-6-ol,
10 tive factor for leukoderma in vivo, the para-substituted phenol 4-tertiary butyl phenol was chosen to
11 a wide range of synthetically important a-(m-substituted phenol)-a,B-unsaturated ketones, featuring a
12                          In the case of para-substituted phenols, after reaction of a dilithio phenol
13 with examples of homogeneous oxidations of a substituted phenol and of cyclohexene by molecular O(2)
14  is moderately more reactive toward HAT with substituted phenol and shows superior activity in OAT.
15 nd that PsiK has good activity on a range of substituted phenols and benzenediols beyond its native s
16 ation in the ESI source via deprotonation of substituted phenols and benzoic acids and explore correl
17    A formal Betti reaction between variously substituted phenols and benzophenone-derived imines to a
18                          Functionalized acyl-substituted phenols and catechols were obtained in 29-97
19  concentrations of one of a series of singly substituted phenols, and it is possible to derive bimole
20                                     Valuable substituted phenols are accessible via the selective dec
21                            A variety of para-substituted phenols are amenable to this methodology, af
22                    Only p-nitro- or p-chloro-substituted phenols are hydroxylated twice.
23 d ligands, as all dissociation constants for substituted phenols are larger than for the wild type en
24                        The acidities of most substituted phenols are linearly related to those of the
25                        The readily available substituted phenols are used as starting materials in th
26                                       When 2-substituted phenols are used as substrates, [RhCl(PPh3)3
27 utants, many of which (e.g., bisphenol A and substituted phenols) are known to be insufficiently remo
28 -phase formation of SOA from a single highly substituted phenol as a function of liquid water content
29 ,2-transposition approach is limited to para-substituted phenols bearing electron-donating groups.
30        substituted 2-hydroxybenzophenones, p-substituted phenols, benzyl and benzoic acid were found.
31                                              Substituted phenols bind tightly to the active site of t
32                             Hydroxylation of substituted phenols by flavin-dependent monooxygenases i
33 e indium-catalyzed regiospecific coupling of substituted phenol derivatives and quaternary peroxyoxin
34                                       Highly substituted phenol derivatives were obtained in high yie
35                                      Three m-substituted phenol derivatives, each with a labile benzy
36 peroxyoxindoles afforded C2 or C4 2-oxindole-substituted phenol derivatives.
37 The presence of polar co-adsorbates, such as substituted phenols, enhances the hydrogenation rate of
38                                      Various substituted phenols exhibiting antioxidant character wer
39                                     The para-substituted phenol gave monohalogenated product with goo
40 ion, an indole or benzimidazole and an ortho substituted phenol group were also essential components
41                    A new family of routes to substituted phenols has been developed.
42    The gas-phase acidities of meta- and para-substituted phenols have been calculated at the B3LYP/6-
43 ases was characterized by the separations of substituted phenols (i.e., nitrophenol and resorcinol) a
44 ase-mediated apoptosis-inducing effect of 51 substituted phenols in a murine leukemia cell line (L121
45 ne (DBU) at room temperature, generates meta-substituted phenols in which the newly introduced meta s
46                            The presence of p-substituted phenols inhibited ClO4(-) formation rates be
47                                    For ortho-substituted phenols, initial incorporation of a benzotri
48 addition to p-quinone methides for accessing substituted phenols is disclosed.
49 tive site of the enzyme leading to loss of a substituted phenol leaving group and generation of a rea
50 he conditions was proven by reacting various substituted phenols, naphthols, and tyrosine derivatives
51  varied by altering the pKa of the departing substituted phenol or thiophenol in either a diethyl pho
52 unds regulating these behaviors are purines, substituted phenols, or cholesteryl esters.
53                   Protection of a variety of substituted phenols proceeds in good to excellent yield.
54 ction of phenols with alcohols to form ortho-substituted phenol products.
55                                     the para-substituted phenol radical-cations and the corresponding
56 or effect on the electronic structure of the substituted phenol radical.
57 roxylates a broad range of chloro- and nitro-substituted phenols, resorcinols, and catechols.
58 ve coupling of unsubstituted, mono- and poly substituted phenols that have been considered beyond the
59  but there are no rate constants with highly substituted phenols that have high Henry's law constants
60 ditions and allows accessing trifluoromethyl-substituted phenols that were not available by classical
61                                   For methyl-substituted phenols, the presence of methyl substituents
62               The regiodivergent addition of substituted phenols to allylic oxides has been demonstra
63          Control of 1,2- and 1,4-addition of substituted phenols to allylic oxides is achieved by int
64                    Probing the reactivity of substituted phenols toward the nitritocopper(II) cryptat
65 -methoxymethyl-5-halo-(S)-tyrosines and para-substituted phenols under acid-catalyzed reaction condit
66                   Direct irradiation of para-substituted phenols under N(2) atmosphere in homogeneous
67 onship determined from hydroxylation of para-substituted phenols under steady-state turnover has a ne
68 a(2)-O(2)N)(ClO(4))(2) (3), also reacts with substituted phenols via primary electron transfer from t
69 r the synthesis of C2 or C4 benzoxazin-3-one-substituted phenols via skeletal rearrangement is descri
70                   Terpenylation reactions of substituted phenols were used to prepare cannabidiol and
71 (PMC), 2,6-dimethyl- and 2,6-di-tert-butyl-4-substituted phenols) were investigated by laser flash ph
72     The binding constants (K(b)) of the para-substituted phenols with the surfactant were also measur
73 , we investigated the kinetics of six highly substituted phenols with the triplet excited state of 3,
74 piperdine- N-hydroxide (TEMPOH) and the para-substituted phenols (X)ArOH (X = para substituent NO(2),