ライフサイエンスコーパス: 1,2-dichloroethane

1 izations of cis-enediynes (see scheme; DCE = 1,2-dichloroethane).

2 ith BF3.Et2O and excess pyrrole in refluxing 1,2-dichloroethane.

3 basic solvents benzene, dichloromethane, and 1,2-dichloroethane.

4 ,6-TCP) to 4-CP, and tetrachloroethene (PCE)/1,2-dichloroethane (1,2-DCA) completely to ethene.

5 1,2-Dichloroethane (1,2-DCA) is a chlorinated solvent cl

6 both aerobic and anaerobic biodegradation of 1,2-dichloroethane (1,2-DCA) using five microbial cultur

7 tionation during anaerobic biodegradation of 1,2-dichloroethane (1,2-DCA) via dihaloelimination by De

8 actionation during aerobic biodegradation of 1,2-dichloroethane (1,2-DCA) via oxidative cleavage of a

9 ollutants under laboratory conditions, e.g., 1,2-dichloroethane, 1,2,3-trichloropropane and gamma-hex

10 The presence of 1,2-dichloroethane (10mgL(-1)) was proved unambiguously

11 on of other environmental pollutants such as 1,2-dichloroethane (72 years), paraoxon (13 months), atr

12 However, monomerization of CP 3 in dry 1,2-dichloroethane affords bright green diamagnetic Co(I

13 hancements were also obtained in the solvent 1,2-dichloroethane, although the analysis of the system

14 ethyl chloride and hydroxide ion and between 1,2-dichloroethane and acetate in solution.

15 ransfer voltammetry at the interface between 1,2-dichloroethane and an aqueous buffer solution or und

16 conditions induced by osmocene dissolved in 1,2-dichloroethane and the subsequent water splitting by

17 that were made for 4-chlorotetrahydropyran, 1,2-dichloroethane, and benzyl alcohol have also confirm

18 tion of water-solvent systems, viz: octanol, 1,2-dichloroethane, and cyclohexane.

19 methylsulfoxide, acetonitrile, nitromethane, 1,2-dichloroethane, and dichloromethane, carried out usi

20 of the DhlA structures using the substrate, 1,2-dichloroethane, and halide ions as probes.

21 n in toluene, THF, tetrahydropyran, i-PrOAc, 1,2-dichloroethane, and MeCN with k(rel) of 7-16.

22 s are uncompetitive inhibitors of XaDHL with 1, 2-dichloroethane as the varied substrate at pH 8.2 (C

23 uCl2(p-cymene)}2], AgSbF6, and (NH4)2S2O8 in 1,2-dichloroethane at 100 degrees C for 24 h to afford o

24 s determined for the duplex trimer by ITC in 1,2-dichloroethane at 20 degrees C.

25 s determined for the duplex trimer by ITC in 1,2-dichloroethane at 20 degrees C.

26 ydes in the presence of 30 mol % BF3.OEt2 in 1,2-dichloroethane at 80 degrees C affords a novel class

27 The S(N)2 displacement of Cl(-) from 1,2-dichloroethane by acetate (CH(3)CO(2)(-)) in water a

28 inetic tests revealed that dechlorination of 1,2-dichloroethane by the consortium was strongly inhibi

29 e chemically stable solution of this salt in 1,2-dichloroethane can be used as "diazonium ink".

30 Although both vinyl chloride and 1,2-dichloroethane could be simultaneously transformed t

31 actor (MBR) was tested for bioremediation of 1,2-dichloroethane (DCA) in groundwater.

32 , has been used to elucidate the reaction of 1, 2-dichloroethane (DCE) with the carboxylate of Asp-12

33 S(N)2 displacement reaction of chloride from 1,2-dichloroethane (DCE) by nucleophilic attack of the c

34 phthalenesulfonate (DNNS) at polarized water/1,2-dichloroethane (DCE) interfaces, i.e., sDNNS(-) (DCE

35 ) dissolved in a tetrahydrofuran (THF) and a 1,2-dichloroethane (DCE) solution, respectively, using p

36 r as well as acetonitrile and cyclohexane in 1,2-dichloroethane (DCE).

37 are reported in the current-time response of 1,2-dichloroethane(DCE)|water(W) submilli-interfaces aft

38 nors and 1,2,4,5-tetracyanobenzene (TCNB) in 1,2-dichloroethane (DCLE) exhibit a mirror image relatio

39 transformed to ethene, prolonged exposure to 1,2-dichloroethane diminished the vinyl chloride transfo

40 DBU=1,8-diazabicyclo[5.4.0]undec-7-ene, DCE=1,2-dichloroethane, DMS=dimethylsulfide).

41 ly varying polarities: cyclohexane, toluene, 1,2-dichloroethane, ethyl acetate, acetone, acetonitrile

42 ur detectable reductive dehalogenases during 1,2-dichloroethane exposure, suggesting that it catalyze

43 etween two immiscible electrolyte solutions, 1,2-dichloroethane-H2O.

44 Organic haloalkanes, such as 1,2-dichloroethane, have a negligible interfering effect

45 1) Ru(bpy)(3)(2+) transfer through the water/1,2-dichloroethane interface and (2) electrodeposition o

46 odeposition of Pd nanoparticles at the water/1,2-dichloroethane interface.

47 ase in transfer of propranolol at an aqueous-1,2-dichloroethane interface.

48 resence of scandium or ytterbium triflate in 1,2-dichloroethane or a cosolvent mixture of 1/9 THF/dic

49 The transformations were performed in 1,2-dichloroethane or acetonitrile under reflux and gave

50 ost detains three molecules each of CHCl(3), 1,2-dichloroethane, or isopropyl chloride.

51 A 1,2-dichloroethane solution containing a commercially av

52 ned in good to excellent yield by stirring a 1,2-dichloroethane solution of the starting triazene wit

53 bon monoxide) chloride] ion pairs in MeCN or 1,2-dichloroethane solutions.

54 In the more polar solvent 1,2-dichloroethane, some salts form both contact and sol

55 In 1,2-dichloroethane the solution is heterogeneous, while

56 stereochemical memory effect in toluene and 1,2-dichloroethane, the reactions in these solvents can

57 Cp*=C(5)Me(5), DCE=1,2-dichloroethane, THF=tetrahydrofuran.

58 catalyzes the reductive dihaloelimination of 1,2-dichloroethane to ethene.

59 vironmentally important dihaloelimination of 1,2-dichloroethane to ethene.

60 served that increasing the influent ratio of 1,2-dichloroethane to trichloroethene was associated wit

61 (tetrachloromethane) and on TDIROF for 90% (1,2-dichloroethane) to 100% (trichloromethane) of what w

62 lytic amount of anhydrous FeCl3 in refluxing 1,2-dichloroethane underwent tandem Conia-ene and Friede

63 ased and subsequent exposure of the films to 1,2-dichloroethane vapor led to a significant increase i

64 emical extraction of rubidium at micro water|1,2-dichloroethane (w|DCE) and water|room-temperature io

65 of carbon tetrachloride-water (CCl4-H2O) and 1,2-dichloroethane-water (DCE-H2O).

66 The transfer of these analytes across a 1,2-dichloroethane/water interface was studied by cyclic

67 ansfer of tetraethylammonium (TEA(+)) at the 1,2-dichloroethane/water interface.

68 ized poly(vinyl chloride) membrane/water and 1,2-dichloroethane/water interfaces.

69 tions across the interface between water and 1,2-dichloroethane were measured by steady-state voltamm

70 onger chained OCBPs (1,2-dichloropropane and 1,2-dichloroethane) were more frequently found on TDIROF

71 n tobacco resulting in the dehalogenation of 1,2-dichloroethane, which was otherwise recalcitrant.