ライフサイエンスコーパス: CHCl3

7 he optical rotation [[alpha]D +22.8 (c 0.50, CHCl3)] obtained on this material confirmed that the rep

8 ported optical rotation [[alpha]D 0 (c 0.50, CHCl3)]47 was biogenetically unreasonable.

9 chiometric amount of an Fl-peptide through a CHCl3 layer.

10 edioxy linkers for the CHCl3@1, CHCl3@3, and CHCl3@4 complexes, whereas the GTT conformation was foun

11 ferent reference standards for both CCl4 and CHCl3 (two of each).

12 hods and laboratories, samples from CCl4 and CHCl3 degradation experiments were analyzed and calibrat

13 topologue ions CCl3, CCl2, CCl (of CCl4) and CHCl3, CHCl2, CHCl (of CHCl3), respectively.

14 It is more soluble in CH3OH and CHCl3 than bilirubin, which is insoluble in CH3OH but so

15 +)-camphorato) Eu(III) complexes in EtOH and CHCl3 solutions substantiating the stereospecific format

16 ine thiolactone with n-butylamine in THF and CHCl3.

17 h methanolic ammonia and partitioned between CHCl3 and water.

18 In both CHCl3 and H2O, the presence of the five-membered ring at

19 spatial variability relative to C2H6, C2Cl4, CHCl3, and CH3Cl.

20 nder conditions of phase-transfer catalysis (CHCl3, KOH, tetramethylammonium bromide), with sonicatio

21 tigated with a series of halomethanes (CCl4, CHCl3, CH2Cl2, and CH3Cl) using a FA-SIFT instrument.

22 t of solubility in organic solvents (CH2Cl2, CHCl3) is observed for n >/= 8, and in the dialkyl serie

23 perties of the liquid media (toluene, CHCl3, CHCl3/CHX, and CHX/THF), spherical, rod-like, fibrous, a

24 of 13 (>pKa(2, AA) of 11.79) and chloroform (CHCl3) was a transformation byproduct of CCl(4).

25 CH3CN and 3.4 x 10(5) M(-1) in 10% v/v DMSO/CHCl3).

26 Quantitative analysis for CHCl3 and CH2Cl2 have also been demonstrated.

27 aneously resolve during crystallization from CHCl3/acetonitrile, and CD spectroscopy and optical rota

28 e dissolved into halogenated solvents (e.g., CHCl3, CH2Cl2) to enable instant detection of gamma radi

29 , then it was treated with a mixture of H2O: CHCl3 and ultrasonic vibration, were used to effectively

30 In CHCl3 containing pyridine (py) or 1,10-phenanthroline (p

31 In CHCl3 solutions, the isomers are subject to reversible i

32 In CHCl3, these products were the respective alkyne, thiant

33 gle-iron shape was still significant (25% in CHCl3, 29% in H2O).

34 yzed by [Ru]NCCH3(+) ([Ru] = Cp(PPh3)2Ru) in CHCl3 generates a diastereomeric mixture of the substitu

35 be predominant in both environments (42% in CHCl3, 38% in H2O), but the population of the angle-iron

36 When solutions of adducts in CHCl3 and MeCN were deposited on activated alumina, elim

37 has shown that both in DMPC vesicles and in CHCl3: MeOH the protein adopts a highly helical secondar

38 lphosphonium tetrafluoroborate or bromide in CHCl3 under mild conditions to give 1-(N-acylamino)alkyl

39 btained transmission FTIR spectra of EmrE in CHCl3:MeOH, DMPC vesicles, and Escherichia coli lipid ve

40 mined to be the large increase in entropy in CHCl3 as a result of the switching.

41 However, in the absence of ligands in CHCl3 and other nonpolar solvents, OsO4 is unreactive to

42 for bilirubin) and approximately 3 mg/mL in CHCl3 (vs approximately 0.6 mg/mL for bilirubin).

43 ates that 1, like bilirubin, is monomeric in CHCl3, and NMR studies show that the most stable structu

44 er chlorine isotope effects were observed in CHCl3 (epsilonC = -7.7 per thousand, epsilonCl = -2.6 pe

45 nformations with the angle-iron preferred in CHCl3 and the U-shape preferred in H2O.

46 ionally stable than 1, racemizing rapidly in CHCl3 (t1/2(rac) = 1.9 h, rt), and with a moderate rate

47 , which is insoluble in CH3OH but soluble in CHCl3.

48 (QDs) and tetracyanoquinodimethane (TCNQ) in CHCl3 dispersions.

49 f Bader's theory (AIM method) reveal that in CHCl3 solution the relative stability of the regioisomer

50 In a mixture of MeOH/CHCl3, the domino cyclization of 1 further affords 14a,

51 -trien)](+) complexes and solvent molecules (CHCl3, CHBr3, or CH2Br2) intercalated between the 2D oxa

52 Notably, CHCl3 is a convenient and safe alternation of CO gas, pr

53 l2, CCl (of CCl4) and CHCl3, CHCl2, CHCl (of CHCl3), respectively.

54 approximately 1.7) suggests deprotonation of CHCl3 as the rate-limiting step.

55 method can also be applied for detection of CHCl3 in water.

56 After evaporation of CHCl3, the enriched phase was analyzed.

57 With the exception of CHCl3, these changes are reversible.

58 G(d,p) level of theory employing the IEF-PCM CHCl3 solvation model were also performed.

59 OH)4(2-), at rates close to that found in py/CHCl3.

60 asured kinetic isotope effect (initial rate (CHCl3)/rate (CDCl3) approximately 1.7) suggests deproton

61 chloroform with high adsorption selectivity (CHCl3 /EA >2000 for example), implying a potential appli

62 d, filled either by the cations and solvent (CHCl3) molecules and/or by interpenetration (up to 4-fol

63 their solutions in apolar organic solvents (CHCl3, benzene) and even in the presence of 10% MeOH.

64 n of the three ethylenedioxy linkers for the CHCl3@1, CHCl3@3, and CHCl3@4 complexes, whereas the GTT

65 rmation was found the most favorable for the CHCl3@2 complex.

66 in standard deviations of 0.2 per thousand (CHCl3) and 0.4 per thousand (CCl4), which are only about

67 By performing a solvent switch from Et2 O to CHCl3 , efficient 1,2-metalate rearrangement of the inte

68 In two such mutants, the spin response to CHCl3 is absent.

69 bic properties of the liquid media (toluene, CHCl3, CHCl3/CHX, and CHX/THF), spherical, rod-like, fib

70 rachloromethane (CCl4) and trichloromethane (CHCl3) was explored by both, gas chromatography-isotope

71 ated VOX compounds such as trichloromethane (CHCl3).

72 enzoates from aryl(hetero)aryl halides using CHCl3 as the carbonyl source in the presence of KOH.

73 In addition, the reactions of CHCl*- with CHCl3 and CH2Cl2 form minor amounts of Cl2*- and Cl-.

74 single crystals have been intercalated with CHCl3 and CHBr3 in order to expand the lattice.