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1 ions of cis-enediynes (see scheme; DCE = 1,2-dichloroethane).
2 arison to other chlorinated solvents such as dichloroethane.
3 BF3.Et2O and excess pyrrole in refluxing 1,2-dichloroethane.
4 ing of Zn(II) tetraphenylporphyrin to CN- in dichloroethane.
5 c solvents benzene, dichloromethane, and 1,2-dichloroethane.
6 on of 10 mM valinomycin and 10 mM ETH 500 in dichloroethane.
7 r results were observed for 1,2-dibromo- and dichloroethanes.
8 ; 1,1,1-trichloroethane (1,1,1-TCA); and 1,1-dichloroethane (1,1-DCA), range from -26.5 per thousand
11 aerobic and anaerobic biodegradation of 1,2-dichloroethane (1,2-DCA) using five microbial cultures.
12 ation during anaerobic biodegradation of 1,2-dichloroethane (1,2-DCA) via dihaloelimination by Dehalo
13 onation during aerobic biodegradation of 1,2-dichloroethane (1,2-DCA) via oxidative cleavage of a C-H
14 tants under laboratory conditions, e.g., 1,2-dichloroethane, 1,2,3-trichloropropane and gamma-hexachl
16 f other environmental pollutants such as 1,2-dichloroethane (72 years), paraoxon (13 months), atrazin
17 However, monomerization of CP 3 in dry 1,2-dichloroethane affords bright green diamagnetic Co(III)(
18 ements were also obtained in the solvent 1,2-dichloroethane, although the analysis of the system is c
20 fer voltammetry at the interface between 1,2-dichloroethane and an aqueous buffer solution or undilut
22 ditions induced by osmocene dissolved in 1,2-dichloroethane and the subsequent water splitting by the
23 t were made for 4-chlorotetrahydropyran, 1,2-dichloroethane, and benzyl alcohol have also confirmed u
24 IEs measured in CCl(4), CHCl(3), CH(2)Cl(2), dichloroethane, and chlorobenzene at -23 degrees C showe
26 ylsulfoxide, acetonitrile, nitromethane, 1,2-dichloroethane, and dichloromethane, carried out using v
30 heated as a dilute solution in triflic acid/dichloroethane, anthracene undergoes conversion to phena
31 uncompetitive inhibitors of XaDHL with 1, 2-dichloroethane as the varied substrate at pH 8.2 (Cl-, K
32 (p-cymene)}2], AgSbF6, and (NH4)2S2O8 in 1,2-dichloroethane at 100 degrees C for 24 h to afford ortho
35 in the presence of 30 mol % BF3.OEt2 in 1,2-dichloroethane at 80 degrees C affords a novel class of
36 of the nucleophilic substitution reaction of dichloroethane by a carboxylate group in haloalkane deha
37 The S(N)2 displacement of Cl(-) from 1,2-dichloroethane by acetate (CH(3)CO(2)(-)) in water and b
38 ic tests revealed that dechlorination of 1,2-dichloroethane by the consortium was strongly inhibited
40 reaction of the nucleophilic displacement of dichloroethane catalyzed by haloalkane dehalogenase.
41 trifluoromethanesulfonic acid (TfOH), 1 M in dichloroethane, catalyzes these rearrangements, with slo
44 2 displacement reaction of chloride from 1,2-dichloroethane (DCE) by nucleophilic attack of the carbo
45 xychlorocarbene (1-AdOCCl) were generated in dichloroethane (DCE) by photolysis of the appropriate di
46 alenesulfonate (DNNS) at polarized water/1,2-dichloroethane (DCE) interfaces, i.e., sDNNS(-) (DCE) +
47 ssolved in a tetrahydrofuran (THF) and a 1,2-dichloroethane (DCE) solution, respectively, using pulse
48 been used to elucidate the reaction of 1, 2-dichloroethane (DCE) with the carboxylate of Asp-124 at
49 ns carried out in CD2Cl2/CD3OD (9/1, v/v) or dichloroethane (DCE), as well as single crystal X-ray di
50 luoromethanesulfonic acid (TfOH), ca. 1 M in dichloroethane (DCE), provides reliable catalytic reacti
52 reported in the current-time response of 1,2-dichloroethane(DCE)|water(W) submilli-interfaces after i
53 and 1,2,4,5-tetracyanobenzene (TCNB) in 1,2-dichloroethane (DCLE) exhibit a mirror image relationshi
54 sformed to ethene, prolonged exposure to 1,2-dichloroethane diminished the vinyl chloride transformin
57 arying polarities: cyclohexane, toluene, 1,2-dichloroethane, ethyl acetate, acetone, acetonitrile, an
58 etectable reductive dehalogenases during 1,2-dichloroethane exposure, suggesting that it catalyzes th
61 idation of the quinoidal bisdithiazole BT in dichloroethane in the presence of [Bu4N][GaBr4] affords
62 u(bpy)(3)(2+) transfer through the water/1,2-dichloroethane interface and (2) electrodeposition of Pd
65 nce of scandium or ytterbium triflate in 1,2-dichloroethane or a cosolvent mixture of 1/9 THF/dichlor
66 The transformations were performed in 1,2-dichloroethane or acetonitrile under reflux and gave the
68 The combination of solvents (dichlorobenzene-dichloroethane) plays a crucial role in achieving quanti
69 s a function of the mole fraction of MeOH in dichloroethane showed that the homoadamantyl chloride io
71 in good to excellent yield by stirring a 1,2-dichloroethane solution of the starting triazene with Cu
73 Cl(-)] ion pairs were generated in methanol/dichloroethane solutions, with R(+) as the 1-bicyclo[2.2
78 reochemical memory effect in toluene and 1,2-dichloroethane, the reactions in these solvents can be c
82 ed that increasing the influent ratio of 1,2-dichloroethane to trichloroethene was associated with ec
83 trachloromethane) and on TDIROF for 90% (1,2-dichloroethane) to 100% (trichloromethane) of what was p
84 c amount of anhydrous FeCl3 in refluxing 1,2-dichloroethane underwent tandem Conia-ene and Friedel-Cr
85 and subsequent exposure of the films to 1,2-dichloroethane vapor led to a significant increase in th
86 al extraction of rubidium at micro water|1,2-dichloroethane (w|DCE) and water|room-temperature ionic
87 hannel deformation when the welding solvent (dichloroethane) was applied between the two chips during
89 The transfer of these analytes across a 1,2-dichloroethane/water interface was studied by cyclic vol
92 s across the interface between water and 1,2-dichloroethane were measured by steady-state voltammetry
93 r chained OCBPs (1,2-dichloropropane and 1,2-dichloroethane) were more frequently found on TDIROF.
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