ライフサイエンスコーパス: substituted phenol

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1 ropofol, an intravenous, strongly lipophilic-substituted phenol.

2 rotein family catalyze the oxidation of para-substituted phenols.

3 r products; syringol, guaiacol, phenols, and substituted phenols.

4 these surface bound species by reaction with substituted phenols.

5 ues is achieved from readily available ortho-substituted phenols.

6 of VAO and related enzymes that oxidize para-substituted phenols.

7 e Grignard addition so as to generate highly substituted phenols.

8 enols (2,6-dimethyl- and 2,6-di-tert-butyl-4-substituted phenols, 2,2,5,7,8-pentamethylchroman-6-ol,

9 tive factor for leukoderma in vivo, the para-substituted phenol 4-tertiary butyl phenol was chosen to

10 In the case of para-substituted phenols, after reaction of a dilithio phenol

11 with examples of homogeneous oxidations of a substituted phenol and of cyclohexene by molecular O(2)

12 is moderately more reactive toward HAT with substituted phenol and shows superior activity in OAT.

13 ation in the ESI source via deprotonation of substituted phenols and benzoic acids and explore correl

14 concentrations of one of a series of singly substituted phenols, and it is possible to derive bimole

15 Only p-nitro- or p-chloro-substituted phenols are hydroxylated twice.

16 d ligands, as all dissociation constants for substituted phenols are larger than for the wild type en

17 The acidities of most substituted phenols are linearly related to those of the

18 The readily available substituted phenols are used as starting materials in th

19 When 2-substituted phenols are used as substrates, [RhCl(PPh3)3

20 utants, many of which (e.g., bisphenol A and substituted phenols) are known to be insufficiently remo

21 Substituted phenols bind tightly to the active site of t

22 Highly substituted phenol derivatives were obtained in high yie

23 Three m-substituted phenol derivatives, each with a labile benzy

24 Various substituted phenols exhibiting antioxidant character wer

25 The para-substituted phenol gave monohalogenated product with goo

26 ion, an indole or benzimidazole and an ortho substituted phenol group were also essential components

27 A new family of routes to substituted phenols has been developed.

28 The gas-phase acidities of meta- and para-substituted phenols have been calculated at the B3LYP/6-

29 ases was characterized by the separations of substituted phenols (i.e., nitrophenol and resorcinol) a

30 ase-mediated apoptosis-inducing effect of 51 substituted phenols in a murine leukemia cell line (L121

31 ne (DBU) at room temperature, generates meta-substituted phenols in which the newly introduced meta s

32 The presence of p-substituted phenols inhibited ClO4(-) formation rates be

33 For ortho-substituted phenols, initial incorporation of a benzotri

34 tive site of the enzyme leading to loss of a substituted phenol leaving group and generation of a rea

35 varied by altering the pKa of the departing substituted phenol or thiophenol in either a diethyl pho

36 unds regulating these behaviors are purines, substituted phenols, or cholesteryl esters.

37 Protection of a variety of substituted phenols proceeds in good to excellent yield.

38 ction of phenols with alcohols to form ortho-substituted phenol products.

39 or effect on the electronic structure of the substituted phenol radical.

40 roxylates a broad range of chloro- and nitro-substituted phenols, resorcinols, and catechols.

41 ditions and allows accessing trifluoromethyl-substituted phenols that were not available by classical

42 The regiodivergent addition of substituted phenols to allylic oxides has been demonstra

43 Control of 1,2- and 1,4-addition of substituted phenols to allylic oxides is achieved by int

44 -methoxymethyl-5-halo-(S)-tyrosines and para-substituted phenols under acid-catalyzed reaction condit

45 onship determined from hydroxylation of para-substituted phenols under steady-state turnover has a ne

46 Terpenylation reactions of substituted phenols were used to prepare cannabidiol and

47 (PMC), 2,6-dimethyl- and 2,6-di-tert-butyl-4-substituted phenols) were investigated by laser flash ph

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