ライフサイエンスコーパス: dimethyl ether

1 recycling of carbon dioxide to methanol and dimethyl ether.

2 olvents containing a hydrogen bond acceptor, dimethyl ether.

3 e for the C-H bonds of methane, methanol, or dimethyl ether.

4 was modeled with Bu(3)Sn-H and prekinamycin dimethyl ether along with prekinamycin itself.

5 Propylene, dimethyl ether, ammonia, R-152a, propane, and HFE-152a a

6 The alkanes and dimethyl ether analyses were performed by headspace-gas

7 del systems (N-methylpyridinium complexes of dimethyl ether and dimethyl phosphate anion) provide qua

8 ed reactions, the dehydration of methanol to dimethyl ether and the total methane oxidation reactions

9 solvent removal, the sodide is dissolved in dimethyl ether and transferred through a frit into a sep

10 The products, methanol, dimethyl ether, and CO2, were desorbed with the passage

11 yclopentane, trifluoroethane, fluoromethane, dimethyl ether, and difluoromethane at ambient temperatu

12 transformations into fuels such as methanol, dimethyl ether, and varied products including synthetic

13 and careful tests, we show that methanol and dimethyl ether are apparently unreactive on the two most

14 of CO2 to formate/formic acid, methanol, and dimethyl ether are thoroughly reviewed, with special emp

15 iX.E, LiX.2E, and LiX.3E (X = F, Cl, Br; E = dimethyl ether as a model for THF).

16 t 6-31+g(d) using RLi coordinated with three dimethyl ethers as a computational model for RLi in THF.

17 ed and the reductive lithiation performed in dimethyl ether at -70 degrees C.

18 element of the new ligands is their acyclic dimethyl ether backbone in lieu of the (isopropylidene)

19 s studied by use of a tetra(ethylene glycol) dimethyl ether-based electrolyte.

20 n a highly convergent synthesis of radicicol dimethyl ether but failed in the removal of the two aryl

21 of C-H activation of methane, methanol, and dimethyl ether by [(N-N)PtMe(TFE-d(3))](+) ((N-N) = ArN=

22 e pendant tetradentate ligand in the masked (dimethyl ether) catechol form, and kinetic pH-rate profi

23 s or even from the air itself to methanol or dimethyl ether (DME) and their varied products can be ac

24 Dimethyl ether (DME) has been considered as a promising

25 explored in the electrochemical oxidation of dimethyl ether (DME) on platinum.

26 y steps required for catalytic combustion of dimethyl ether (DME) on Pt clusters were determined by c

27 ep controls catalytic carbonylation rates of dimethyl ether (DME) to methyl acetate.

28 for one-step conversion of synthesis gas to dimethyl ether (DME) was imaged simultaneously and in si

29 Recycling of CO(2) into methanol, dimethyl ether (DME), and derived fuels and materials is

30 eal solvents (usually in mixtures of THF and dimethyl ether, ether, and 2,5-dimethyltetrahydrofuran).

31 associative routes mediate the formation of dimethyl ether from methanol on zeolitic acids at the te

32 4'-hexahydroxy-1,1'-biphenyl-6,6'-dimethanol dimethyl ether [HBDDE]) but not PKC-beta II (LY379196) d

33 ls including syngas, methanol, formaldehyde, dimethyl ether, heavier hydrocarbons, aromatics, and hyd

34 Qaw was calculated from the uptake of dimethyl ether in the anatomic dead space minus the most

35 her or other solvent, and evaporation of the dimethyl ether in vacuo, the alpha-methylstyrene is adde

36 Intact poly(ethylene glycol) dimethyl ether is identified as the electrolyte degradat

37 gy of dimerization of fluoromethyllithium in dimethyl ether is predicted to be -0.9 kcal mol(-)(1), w

38 ouble Baeyer-Villiger reaction of quinizarin dimethyl ether is viable, directly providing the dibenzo

39 It's dehydration product, dimethyl ether, is a diesel fuel and liquefied petroleum

40 by a combination of specific coordination of dimethyl ether ligands on each lithium and "dielectric s

41 oxide ratios being suitable for synthesis of dimethyl ether, methanol and for the Fischer-Tropsch pro

42 f the carbenoid reactions of alpha-lithiated dimethyl ether (methoxymethyllithium) and the intramolec

43 in the lithium dimethylaminoborohydride bis(dimethyl ether) microsolvate.

44 were calculated in the gas phase and for the dimethyl ether microsolvated molecules.

45 and reactions of compounds in which the O of dimethyl ether or acetone has been replaced by NH, PH, o

46 d by the use of microsolvation with explicit dimethyl ether or THF ligands and by the combined use of

47 recedented insight into the carbonylation of dimethyl ether over Mordenite is provided through the id

48 a previous study of idealized disiloxane and dimethyl ether parent species to fully methylated deriva

49 ethyl carbonate (EMC), poly(ethylene glycol) dimethyl ether, poly(ethylene glycol) ethyl methyl ether

50 Dimethyl ether/poly(hydrogen fluoride) (DMEPHF), are sta

51 Dimethyl ether pyrolysis (2% CH3OCH3/Ar) was observed be

52 reliminary monitoring of propane, butane and dimethyl ether residues, in cakes and chocolate after sp

53 rbenoids are studied in the gas phase and in dimethyl ether solvent.

54 f mixtures of water and tetraethylene glycol dimethyl ether (TEGDE), a methyl-terminated derivative o

55 Qaw was measured with the dimethyl ether uptake technique, which reflects blood fl

56 Release kinetics of propane, butane and dimethyl ether were measured over one day with sprayed f

57 Reaction of dimethyl ether with 2(TFE) proceeds similarly (K(eq) = 0