ライフサイエンスコーパス: diethyl ether

1 rude protein, Ara h 1, and Ara h 2 than with diethyl ether.

2 ed with n-butyllithium in tetrahydrofuran or diethyl ether.

3 in a suspension of SnCl4.(Et2O)2 complex in diethyl ether.

4 e unsaponifiable fraction was extracted with diethyl ether.

5 ial crystallization of the anti isomers from diethyl ether.

6 t the entire solubility range of LiClO(4) in diethyl ether.

7 dichloroborane adducts of methyl sulfide and diethyl ether.

8 s used as the extraction solvent in place of diethyl ether.

9 acetone and quantitatively transferred into diethyl ether.

10 traction applying the mixture of pentane and diethyl ether 1:2v/v (solvent A) as well as dichlorometh

11 ent polarities (dipole moment - hexane: 0.0, diethyl ether: 2.80, ethyl acetate: 4.40, methanol: 5.10

12 be the unusual reactivity of a highly labile diethyl ether adduct of an asymmetric niobium(V) bis(imi

13 ethoxide with [H(OEt2)2][H2N{B(C6F5)3}2] in diethyl ether afforded [Tl(OEt2)3][H2N{B(C6F5)3}2] (2a),

14 IR spectra of diethyl ether and diethyl sulfide reveal that both molec

15 Other volatile anesthetics, diethyl ether and diisopropyl ether, reduce the quenchin

16 ithium exists as a tetrasolvated tetramer in diethyl ether and exclusively as bis-solvated dimers wit

17 etypal volatile anesthetic molecules such as diethyl ether and halothane.

18 eir progress through subsequent washing with diethyl ether and reactions with measured amounts of wat

19 c molecules, including ethanol, ethanethiol, diethyl ether, and diethyl sulfide, at the Ge(100)-2 x 1

20 The Z isomer is completely dimeric in pure diethyl ether, and mostly dimeric in 3:2 THF/ether, wher

21 or observed aggregation states of the TMEDA, diethyl ether, and THF solvates.

22 anic solvents such as tetrahydrofuran (THF), diethyl ether, and toluene.

23 chieved with ethyl iodide in the presence of diethyl ether as cosolvent; the 1-ethoxyethyl adduct was

24 ions with 15 as the acceptor involved use of diethyl ether as the reaction solvent and 0.2 equiv of T

25 s of reactions of MeLi with benzophenones in diethyl ether at 0 degrees C that furnish methyldiarylme

26 soluble in NMP, they were barely soluble in diethyl ether, because of the free trisaccharide.

27 eduction of molecular nitrogen to ammonia in diethyl ether between -78 and 22 degrees C in a batchwis

28 During the catalytic reduction of diethyl ether, cationic iridium silane complex, [(POCOP)

29 In cardiac SR hexanol, halothane, and diethyl ether caused pronounced increases in the limitin

30 1,3-(SiMe3)2)Zr, with dialkyl ethers such as diethyl ether, CH3OR (R=Et, nBu, tBu), nBu2O, or iPr2O r

31 action with a mixture of dichloromethane and diethyl ether containing lipases and a subsequent concen

32 ium forms of the steroid were extracted with diethyl ether, converted to the C21 acetate derivative,

33 ds invert faster in THF-d(10) compared to in diethyl ether-d(10) as solvent.

34 ive DeltaS(double dagger) values, whereas in diethyl ether-d(10) DeltaS(double dagger) values for inv

35 ounds 6, 7, and 9 are monomeric in THF-d8 or diethyl ether-d10 solution and exhibit one bond 13C1, 6L

36 st to Z-5F-Li, the E isomer is tetrameric in diethyl ether even in the presence of excess HMPA.

37 Diethyl ether extracts, which are expected to contain th

38 Subsequent treatment with diethyl ether fails to remove any surface species, but i

39 obtained by performing the same reaction in diethyl ether followed by lyphilization of 2 from benzen

40 The pollen coat was extracted with diethyl ether from the pollen of maize (Zea mays L.), an

41 ted separately in a two-step procedure using diethyl ether/hexane (90:10, v/v) in the first step to e

42 nic solvents (methanol, ethanol, acetone and diethyl ether) in isolation of these compounds to gain i

43 y mediates sedation by ethanol vapor but not diethyl ether, indicating that the observed NPF/NPFR1 ac

44 similar propyl carbamate; (2) extraction by diethyl ether instead of more toxic dichloromethane, and

45 A mixed species involving the [H(H(2)O)(diethyl ether)](+) ion has also been isolated.

46 t-butylphenyl)lithium, which is slow in pure diethyl ether, is virtually quantitative in heptane cont

47 aining ionic clusters of lithium perchlorate-diethyl ether, less energy is required to transfer the m

48 her to 84.5% in a 4.14 M lithium perchlorate-diethyl ether (LPDE) solution, a nearly 17-fold increase

49 ment within solutions of lithium perchlorate-diethyl ether (LPDE) was probed by utilizing the extraor

50 cules, or which include water as a model for diethyl ether, may lead to incorrect predictions of the

51 with ethereal and ester donor ligands (THF, diethyl ether, MTBE, THP, tert-butyl acetate) are charac

52 In diethyl ether, N-Boc-2-lithio-2-arylpiperidines have bee

53 general anesthetics hexanol, halothane, and diethyl ether on Ca-ATPase activity and on the oligomeri

54 In solid phase or in the nonpolar solvent (diethyl ether), only one of the three isomers is present

55 tone, or choloroform (1b); toluene (1c); and diethyl ether or ethyl acetate (1d), demonstrate differe

56 After the addition of diethyl ether or other solvent, and evaporation of the d

57 -di-p-anisylformamidinate), with a molecule (diethyl ether) or a cation (tetraethylammonium ion) trap

58 action method was applied using a mixture of diethyl ether-pentane (1:1,w/w) as solvent.

59 C-t-Bu(2) to CrCl(3), MoCl(5), and WCl(6) in diethyl ether produced the complexes M(N=C-t-Bu(2))(4) (

60 Methyl tertbutyl ether and diethyl ether provided the highest extraction recoveries

61 18-crown-6 at -45 degrees C under vacuum in diethyl ether react with CO at -78 degrees C to form col

62 he partial release of the surface-associated diethyl ether; Si-CH3 moieties remain.

63 to the Z-enolate in the poorly coordinating diethyl ether solvent.

64 When organic O-atom donors such as diethyl ether, tetrahydrofuran, benzophenone, and nitrob

65 trahydrofuran, tetrahydropyran, 1,4-dioxane, diethyl ether, tetrahydrothiophene, and 1,3-dithiolane.

66 In diethyl ether the E:Z ratio was 15:1 in favor of the E-e

67 Li or t-BuLi) and/or the solvent (pentane or diethyl ether); the 3-deuterated substrate, 3-Ddman, was

68 fferentiate between common solvents, such as diethyl ether, THF, ethyl acetate, acetone, alcohol, ace

69 keto content of 1 increases from 5% in pure diethyl ether to 84.5% in a 4.14 M lithium perchlorate-d

70 procedure, the crude solids are washed with diethyl ether to afford the pure products, as revealed b

71 Thus, as the medium changes from diethyl ether to one containing ionic clusters of lithiu

72 ed silica gel column eluted with pentane and diethyl ether to separate minor compounds.

73 Consequently, addition of diethyl ether to the reaction mixtures could precipitate

74 Addition of a silylated acetylide to 11 in diethyl ether/trimethylamine gave mainly 22a.

75 Liquid-liquid extraction with diethyl ether was followed by GC-MS for TCE quantificati

76 netic isotope effects for the reactions with diethyl ether were measured.

77 two intermediates with ethyl vinyl ether and diethyl ether were monitored by single- and double-mixin