ライフサイエンスコーパス: methylene chloride

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1 silyl enol ethers are surprisingly stable in methylene chloride.

2 uefortine C were extracted from samples with methylene chloride.

3 l carbamate, and the occupational carcinogen methylene chloride.

4 ond complex between U(H)(+) and HU(H)H(+) in methylene chloride.

5 ronoabsorptometry of Cl2FeS2MoS2FeCl2(2-) in methylene chloride.

6 d 36 cm-1, respectively, relative to that in methylene chloride.

7 with CXF spectra in aqueous solution and in methylene chloride.

8 a 5-congener mixture in relatively volatile methylene chloride, a methylene chloride extract of free

9 kyne, Et(2)Zn, and (S)-1,1'-bi-2-naphthol in methylene chloride allows the generation of an alkynylzi

10 e ket as the freezing points of the solvents methylene chloride and acetonitrile were approached.

11 a functional group, has been investigated in methylene chloride and acetonitrile.

12 k copolymers were assembled by dissolving in methylene chloride and allowing the solvent to evaporate

13 ulfonic (triflic) acid compared with aprotic methylene chloride and sulfolane solutions.

14 uintile of diesel, lead, manganese, mercury, methylene chloride, and an overall measure of metals wer

15 ibrium measurements in trifluoroacetic acid, methylene chloride, and ethyl acetate demonstrated that

16 as explored in three solvents: acetonitrile, methylene chloride, and methanol.

17 chloridate and excess nucleoside in pyridine/methylene chloride at 0 degree C to give 3 in 82% yield.

18 e (for 2) with phosphorus oxychloride in dry methylene chloride at 0 degree C with the addition of tr

19 The particulate matter was extracted using methylene chloride, back extracted into aqueous solution

20 c solvents studied were acetonitrile (MeCN), methylene chloride, chloroform, and tetrahydrofuran (THF

21 mixture of hexafluoro-2-propanol (HFIP) and methylene chloride (DCM) is described.

22 to 8-fluoro-2'-deoxyadenosine using TASF in methylene chloride demonstrates the compatibility of des

23 e common organic solvents evaluated (hexane, methylene chloride, diethylether, chloroform, methylisob

24 ence anions in seven solvents: acetonitrile, methylene chloride, dimethylformamide, tetrahydrofuran,

25 Methylene chloride/ethyl acetate/formic acid (6:10:1, v/

26 in relatively volatile methylene chloride, a methylene chloride extract of freeze-dried mussel (Mytil

27 2, 3-dimethyl-2-butene in the gas phase and methylene chloride extracts of 2,3-dimethyl-2-butanol an

28 igh quantum yields (60-99%) were observed in methylene chloride in addition to large Stokes shifts (9

29 was increased to 0.08-0.24 with 1000 ppm of methylene chloride in the drift gas.

30 Likewise, nine of 24 methylene chloride-induced hepatocellular neoplasms and

31 However, the oxidation of U(H)H in methylene chloride is reversible at higher concentration

32 effects of carbon monoxide (CO) induction by methylene chloride (MC).

33 be selectively prepared simply by selecting methylene chloride or THF as the reaction solvent, respe

34 rs associated with NNK, vinyl carbamate, and methylene chloride, respectively.

35 Sequestration of a methylene chloride solution of the Ds-pip complex from a

36 ions persist for days at room temperature in methylene chloride solution.

37 s observed in toluene, C(6)D(6), heptane, or methylene chloride solutions.

38 PVF = poly(vinylferrocene)) films exposed to methylene chloride solutions.

39 plementary oligoamides in not only nonpolar (methylene chloride) solutions but also highly competitiv

40 the photolysis reactions were carried out in methylene chloride, solvent binding competitive with hyd

41 velengths could be affected by swelling with methylene chloride vapor.

42 mines in N,N-dimethylformamide, methanol, or methylene chloride/water (phase-transfer conditions) yie

43 acid (DCA) and trichloroacetic acid (TCA) in methylene chloride were found to be 3% DCA >> 15% DCA >

44 solvents as revealed by (113)Cd NMR in d(2)-methylene chloride, which displays (111)Cd-(113)Cd coupl

45 solutions of nonhydrated glyoxals (16k-m) in methylene chloride with Deoxofluor produced the tetraflu

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