ライフサイエンスコーパス: cyclohexanol

1 n of alcohols were studied on the example of cyclohexanol.

2 he enantiopure (1S,2S)-2-(1-H-imidazol-1-yl)-cyclohexanol.

3 olvent consisting of 70% 1-dodecanol and 30% cyclohexanol.

4 ot by the addition of an equimolar amount of cyclohexanol.

5 hat is observed at optimal concentrations of cyclohexanol.

6 thylheptyl)phenyl]-trans-4-(3-hydroxyprop yl)cyclohexanol].

7 he oxidation of cyclohexane to cyclohexanone/cyclohexanol (100 degrees C, conversion: 17.7%) is super

8 thylheptyl)phenyl]-trans-4-(3-hydroxyp ropyl)cyclohexanol ([3H]CP55,940) in a concentration-dependent

9 ol (AH5183; (-)-trans-2-[4-phenylpiperidino] cyclohexanol), a drug which blocks the refilling of syna

10 ,1-dimethylheptyl)phenyl]-4-(3-hydroxypropyl)cyclohexanol], a potent cannabinoid that binds with simi

11 functionalized stereoselectively to provide cyclohexanols after oxidation of the carbon-silicon bond

12 l methacrylate in the presence of mixture of cyclohexanol and 1-dodecanol as a porogenic solvent.

13 ith formaldehyde or methane, and on ethanol, cyclohexanol and 1-hydroxymethyl-tetrahydropyran are pre

14 ties >95% are obtained with trans-2-phenyl-1-cyclohexanol and 2,2-diphenylcyclopentanol vinyl ethers.

15 Here, the oxidation of cyclohexane to cyclohexanol and cyclohexanone is used as a model reacti

16 solid-acid-catalyzed phenol alkylation with cyclohexanol and cyclohexene in the apolar solvent decal

17 ignificant migration of the hydroxy group in cyclohexanol and the double bond in cyclohexene with res

18 aturation kinetics for oxidation of ethanol, cyclohexanol, and 1-butanol are quantitatively explained

19 dustrial wastewater bioreactor that utilized cyclohexanol as a sole carbon source.

20 e HBEA catalyse aqueous phase dehydration of cyclohexanol at a rate significantly higher than hydroni

21 ot caused by the limited access of phenol to cyclohexanol, but is due to the absence of a reactive el

22 iation of NADH from the abortive enzyme-NADH-cyclohexanol complex than from the enzyme-NADH complex.

23 For liquid-phase catalytic cyclohexanol dehydration, these SiO(x) sites exhibit up

24 yoxy-methyl-1-cyclo-hexanone to give a vinyl cyclohexanol derivative and (2) a highly stereoselective

25 Thus, it is demonstrated that protonated cyclohexanol dimers dehydrate without the formation of a

26 y accounts for the initial rates of 1-(13) C-cyclohexanol disappearance and the appearance of the dif

27 Synthesis and testing of a series of cyclohexanol ethylpiperazines identified ( S)-(-)- 17i (

28 Consistent with a previous report, cyclohexanol forms initially but then esterifies to cycl

29 acetophenone from 1-phenylethanol oxidation, cyclohexanol from cyclohexane hydroxylation, and cyclohe

30 ethyl-heptyl)-2,6-dimethoxy-phenyl]-3-methyl-cyclohexanol), greatly attenuated leukocyte adhesion in

31 Transient kinetics experiments show that cyclohexanol inhibition is due to a slower rate of disso

32 r condensation, one chiral separation of the cyclohexanol intermediate, an ether formation using a tr

33 yclohexanol sets in only after a majority of cyclohexanol is dehydrated to cyclohexene.

34 rophile as long as a significant fraction of cyclohexanol is present.

35 exemplified by intramolecular dehydration of cyclohexanol, is markedly influenced by steric constrain

36 In the presence of cyclohexanol, its protonated dimers at Bronsted acid sit

37 occurs with myo-inositol-d-galactopyranose, cyclohexanol, mannitol, or glycerol as acyl acceptor.

38 echanism; for both cases, the dehydration of cyclohexanol occurs via an E1 mechanism with the cleavag

39 C spectra show that dehydration of 1-(13) C-cyclohexanol occurs with significant migration of the hy

40 ic and mechanistic study of the reactions of cyclohexanol on zeolite HBEA in 130 degrees C water.

41 sertion in each of the ORFs was screened for cyclohexanol oxidation in E. coli.

42 transposon mutants accumulated a variety of cyclohexanol oxidation intermediates.

43 A region that was essential for cyclohexanol oxidation was localized to a 14-kb fragment

44 Cyclohexanol, phenol, benzoic acid, and phenanthrene fra

45 In contrast, high concentrations of cyclohexanol produce noncompetitive substrate inhibition

46 sandwiched between the two methylenes in the cyclohexanol ring and the hydroxyl group of ethanol hydr

47 oiety and the two flanking methylenes in the cyclohexanol ring of cholesterol.

48 Phenol alkylation with cyclohexanol sets in only after a majority of cyclohexan

49 As phenol and cyclohexanol show similar adsorption strength, this stri

50 netobacter sp. strain SE19, and oxidation of cyclohexanol to adipic acid was demonstrated in recombin

51 encode enzymes catalyzing the conversion of cyclohexanol to adipic acid were identified.

52 he 4-O-5 linkage) is hydrogenated to produce cyclohexanol under conditions investigated.

53 trace [(3)H]-(-)-trans-2-(4-phenylpiperidino)cyclohexanol (vesamicol) with ACh, and Michaelis-Menten

54 potent anticholinergic 2-(4-phenylpiperidino)cyclohexanol (vesamicol, 1) in which the cyclohexyl frag

55 ine transporter ligand 2-(4-phenylpiperidino)cyclohexanol (vesamicol, 1), 22 N-hydroxy(phenyl)alkyl d

56 value up to 98%) synthesis of trisubstituted cyclohexanols was achieved by using a tandem Henry--Mich

57 picomoles of norbenzphetamine and 21 pmol of cyclohexanol were formed per nmol of cyt P450.

58 500 pmol of norbenzphetamine and 58 pmol of cyclohexanol were formed per nmol of cyt P450.

59 ectly produces trans-2-(dimethylphenylsilyl)-cyclohexanol, whereas the less favored boat-like transit

60 )-vesamicol [(-)-trans-2-(4-phenylpiperidino)cyclohexanol], which binds tightly to an allosteric site

61 Acetic acid, butyric acid and cyclohexanol with vinegar, cheese and camphor odours wer