ライフサイエンスコーパス: fluorobenzene

1 Pd-catalyzed arylation of Cr(CO)3-complexed fluorobenzene.

2 (87%) for the polymerization of 1-ethynyl-4-fluorobenzene.

3 pha) induced in the ears using 2,4-dinitro-1-fluorobenzene.

4 sensitization with the hapten 2,4 dinitro-1-fluorobenzene.

5 nduced by local application of 2,4-dinitro-1-fluorobenzene.

6 reviously been sensitized with 2,4-dinitro-1-fluorobenzene.

7 mice during sensitization with 2,4-dinitro-1-fluorobenzene.

8 solvents such as MeCN, dichloromethane, and fluorobenzene.

9 ing the aromatic defluorinative amination of fluorobenzenes.

10 s of 1,4-bis(2-hydroxy-2-methyl-3-butynyl)-2-fluorobenzene 4 have a rich packing structure with four

11 ) (Ar = phenyl, 4-methylbenzene, naphthyl, 4-fluorobenzene, 4-(trifluoromethyl)benzene, 4-methoxybenz

12 The X-ray crystal structures of fluorobenzene 50c and benzoquinone 54 inhibitors complex

13 Its further reaction with fluorobenzene afforded the CAr -H bond activation produc

14 s, all-trans-retinoic acid, or 2-4-dinitro-1-fluorobenzene, all known to induce K6 expression in skin

15 catalysts through an S(N)Ar reaction between fluorobenzene and alcohols, including secondary alcohols

16 material 6 promotes the H/D exchange between fluorobenzene and C(6)D(6) or D(2) as deuterium sources

17 e the introduction of other dopants, such as fluorobenzene and chlorobenzene, shifted the ionization

18 er, benzene-phenol, benzene-toluene, benzene-fluorobenzene, and benzene-benzonitrile are studied by c

19 CCF 3 has a triplet ground state in benzene, fluorobenzene, and hexafluorobenzene.

20 sition of the arene, but are formed when the fluorobenzenes are very electron-deficient, or when chel

21 rs for ether formation from para-substituted fluorobenzenes are well correlated with the electron-don

22 halides, such as chloro-, bromo-, iodo-, and fluorobenzene, behave differently under the same reactio

23 Reaction of 1 with fluorobenzene cleanly forms a mixture of Cp*(2)ZrHF, ben

24 Analysis of the degradation rates of the 12 fluorobenzene congeners showed two trends: slower degrad

25 C(6)D(6), chlorobenzene-d(5), anisole-d(8), fluorobenzene-d(5), toluene-d(8), o-xylene-d(10), m-xyle

26 or no hydrogen-bonding potential, such as 3-fluorobenzene (d3FB), are synthesized and extended by DN

27 that they most likely do not form during the fluorobenzene degradation reaction.

28 Fluorobenzene degraded rapidly (t(1/2) approximately 0.2

29 me intermediates from commercially available fluorobenzene derivatives are discussed.

30 A 13-member library of alkyl-fluorobenzene derivatives was tested in an established b

31 urate correspondence except in the case of p-fluorobenzene derivatives.

32 (t-Bu(3)P)(2)Pd, the coupling with 1-bromo-4-fluorobenzene displays the following rate equation: rate

33 erance to the contact sensitizer 2,4-dinitro-fluorobenzene (DNFB) depends on microbiota/TLRs and eval

34 in infiltration in response to 2,4-dinitro-1-fluorobenzene (DNFB) required Fas ligand (FasL) and perf

35 in with the contact sensitizer 2,4-dinitro-1-fluorobenzene (DNFB) resulted in a 13-fold increase in C

36 tion of the contact sensitizer 2,4 dinitro-1-fluorobenzene (DNFB) to normal skin.

37 Applying 2,4-dinitro-1-fluorobenzene (DNFB) to wild-type mice activated LC migr

38 a reduced response in a model of 2,4-dinitro-fluorobenzene (DNFB)-induced contact hypersensitivity.

39 creatine kinase (CK) inhibitor 2,4-dinitro-1-fluorobenzene (DNFB).

40 Camphorsulfonic acid in warm fluorobenzene facilitates the ortho rearrangement of (al

41 n biphenyl synthesis from phenyl lithium and fluorobenzene in 1940.

42 a nitrogen plasma and +15.7 kJ mol(-1) with fluorobenzene in an air plasma).

43 peptide induced tolerance to 2, 4-dinitro-1-fluorobenzene in both normal and mast cell deficient mic

44 sign, a basic nitrogen and 4-chlorophenoxy-2-fluorobenzene in the substrate branch contribute most to

45 (N)Ar reaction on the deactivated 1-alkoxy-3-fluorobenzene intermediates have been investigated.

46 n nNOS, in which the 2-aminopyridine and the fluorobenzene linker form crucial hydrogen bonds with gl

47 )-5-fluoropyrimidine, or 1,3-di(arylamino)-4-fluorobenzene moiety instead of a 2,4-disubstituted pyri

48 a second, sensitizing dose of 2, 4-dinitro-1-fluorobenzene on uninjected skin.

49 itting indicated that sorption/desorption of fluorobenzene onto the catalyst surface plays an importa

50 somer anions generated from their associated fluorobenzene precursors.

51 The reaction of 1 with variously substituted fluorobenzenes proceeds as an insertion of the nucleophi

52 the electric-field-induced tilt of the polar fluorobenzene ring that directs all of the peripheral ph

53 base pair candidate of this series is the 3-fluorobenzene self-pair, which is replicated with reason

54 e of such reagents, 9 is stable for weeks in fluorobenzene solution, presumably reflecting (i) effect

55 on to [(BDI)Ga(H)-Zn(tmeda)][BAr(4) (F) ] in fluorobenzene solution.

56 mperature reaction of a 3:1 AB/VB mixture in fluorobenzene solvent, while the branched and linear-cha

57 Three fluorobenzenes substituted with meta-triazole groups hav

58 lly followed by application of 2,4-dinitro-1-fluorobenzene to the injected skin surface.

59 arene in the complex (departing) is benzene, fluorobenzene, toluene, o-xylene, m-xylene, or p-xylene

60 for hydrodefluorination and hydrogenation of fluorobenzene under mild aqueous conditions (1 atm of H(

61 rong aryl C-F bonds, including difluoro- and fluorobenzene, using 1 atm of H(2), alkoxide bases, and

62 When 2,4-dinitro-1-fluorobenzene was painted on skin into which splenic den

63 al quaternary salt (10 mol %) as catalyst in fluorobenzene-water.

64 rgetically disfavored in reactions involving fluorobenzenes with a single electron-withdrawing group