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1 ed with n-butyllithium in tetrahydrofuran or diethyl ether.
2  in a suspension of SnCl4.(Et2O)2 complex in diethyl ether.
3 e unsaponifiable fraction was extracted with diethyl ether.
4 ial crystallization of the anti isomers from diethyl ether.
5 t the entire solubility range of LiClO(4) in diethyl ether.
6 rude protein, Ara h 1, and Ara h 2 than with 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 erent anti-solvents: toluene, ethyl acetate, diethyl ether, and chlorobenzene.
20 c molecules, including ethanol, ethanethiol, diethyl ether, and diethyl sulfide, at the Ge(100)-2 x 1
21   The Z isomer is completely dimeric in pure diethyl ether, and mostly dimeric in 3:2 THF/ether, wher
22 or observed aggregation states of the TMEDA, diethyl ether, and THF solvates.
23 anic solvents such as tetrahydrofuran (THF), diethyl ether, and toluene.
24 chieved with ethyl iodide in the presence of diethyl ether as cosolvent; the 1-ethoxyethyl adduct was
25 ions with 15 as the acceptor involved use of diethyl ether as the reaction solvent and 0.2 equiv of T
26 s of reactions of MeLi with benzophenones in diethyl ether at 0 degrees C that furnish methyldiarylme
27 0 mol %) titanium tetrachloride (TiCl(4)) in diethyl ether at room temperature immensely accelerates
28 y, we demonstrate that the locally optimized diethyl ether-based localized-high-concentration electro
29  soluble in NMP, they were barely soluble in diethyl ether, because of the free trisaccharide.
30 eduction of molecular nitrogen to ammonia in diethyl ether between -78 and 22 degrees C in a batchwis
31            During the catalytic reduction of diethyl ether, cationic iridium silane complex, [(POCOP)
32        In cardiac SR hexanol, halothane, and diethyl ether caused pronounced increases in the limitin
33 1,3-(SiMe3)2)Zr, with dialkyl ethers such as diethyl ether, CH3OR (R=Et, nBu, tBu), nBu2O, or iPr2O r
34  furnished the corresponding chromium THF or diethyl ether complexes.
35 action with a mixture of dichloromethane and diethyl ether containing lipases and a subsequent concen
36 ium forms of the steroid were extracted with diethyl ether, converted to the C21 acetate derivative,
37 ds invert faster in THF-d(10) compared to in diethyl ether-d(10) as solvent.
38 ive DeltaS(double dagger) values, whereas in diethyl ether-d(10) DeltaS(double dagger) values for inv
39 ounds 6, 7, and 9 are monomeric in THF-d8 or diethyl ether-d10 solution and exhibit one bond 13C1, 6L
40 s including THF, tert-butylmethyl ether, and diethyl ether; dipolar ligands such as DMF, HMPA, DMSO,
41                  By contrast, nonhalogenated diethyl ether does not interact with entangled photons.
42 st to Z-5F-Li, the E isomer is tetrameric in diethyl ether even in the presence of excess HMPA.
43                                              Diethyl ether extracts, which are expected to contain th
44                    Subsequent treatment with diethyl ether fails to remove any surface species, but i
45  obtained by performing the same reaction in diethyl ether followed by lyphilization of 2 from benzen
46           The pollen coat was extracted with diethyl ether from the pollen of maize (Zea mays L.), an
47 ted separately in a two-step procedure using diethyl ether/hexane (90:10, v/v) in the first step to e
48 nic solvents (methanol, ethanol, acetone and diethyl ether) in isolation of these compounds to gain i
49 y mediates sedation by ethanol vapor but not diethyl ether, indicating that the observed NPF/NPFR1 ac
50  similar propyl carbamate; (2) extraction by diethyl ether instead of more toxic dichloromethane, and
51      A mixed species involving the [H(H(2)O)(diethyl ether)](+) ion has also been isolated.
52 complexes and alkali cations in 98:2 toluene/diethyl ether is fast on the NMR time scale, which suppo
53 hetics, demonstrating that short exposure to diethyl ether is the most effective for long-term immobi
54 t-butylphenyl)lithium, which is slow in pure diethyl ether, is virtually quantitative in heptane cont
55 aining ionic clusters of lithium perchlorate-diethyl ether, less energy is required to transfer the m
56 her to 84.5% in a 4.14 M lithium perchlorate-diethyl ether (LPDE) solution, a nearly 17-fold increase
57 ment within solutions of lithium perchlorate-diethyl ether (LPDE) was probed by utilizing the extraor
58 cules, or which include water as a model for diethyl ether, may lead to incorrect predictions of the
59 s found when 4 L were extracted with hexane, diethyl ether, methanol, or butanol, but activity was ob
60  with ethereal and ester donor ligands (THF, diethyl ether, MTBE, THP, tert-butyl acetate) are charac
61                                           In diethyl ether, N-Boc-2-lithio-2-arylpiperidines have bee
62  general anesthetics hexanol, halothane, and diethyl ether on Ca-ATPase activity and on the oligomeri
63   In solid phase or in the nonpolar solvent (diethyl ether), only one of the three isomers is present
64 tone, or choloroform (1b); toluene (1c); and diethyl ether or ethyl acetate (1d), demonstrate differe
65                        After the addition of diethyl ether or other solvent, and evaporation of the d
66 esults have been obtained considering either diethyl ether or toluene as a solvent, in both cases in
67 -di-p-anisylformamidinate), with a molecule (diethyl ether) or a cation (tetraethylammonium ion) trap
68 action method was applied using a mixture of diethyl ether-pentane (1:1,w/w) as solvent.
69 raditional solvents (tetrahydrofuran-THF and diethyl ether: petroleum ether-DE:PE) and green solvents
70 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) (
71                   Methyl tertbutyl ether and diethyl ether provided the highest extraction recoveries
72  18-crown-6 at -45 degrees C under vacuum in diethyl ether react with CO at -78 degrees C to form col
73 For example, in a 100:0.2 mixture of toluene/diethyl ether, reactions of Ni1 and both Li(+) and Na(+)
74                 In a 98:2 mixture of toluene/diethyl ether, reactions of Ni2 and Cs(+) in the presenc
75 he partial release of the surface-associated diethyl ether; Si-CH3 moieties remain.
76  to the Z-enolate in the poorly coordinating diethyl ether solvent.
77           When organic O-atom donors such as diethyl ether, tetrahydrofuran, benzophenone, and nitrob
78 trahydrofuran, tetrahydropyran, 1,4-dioxane, diethyl ether, tetrahydrothiophene, and 1,3-dithiolane.
79                                           In diethyl ether the E:Z ratio was 15:1 in favor of the E-e
80 Li or t-BuLi) and/or the solvent (pentane or diethyl ether); the 3-deuterated substrate, 3-Ddman, was
81 fferentiate between common solvents, such as diethyl ether, THF, ethyl acetate, acetone, alcohol, ace
82 onditions permitted the elusive synthesis of diethyl ether through reductive elimination, a remarkabl
83  keto content of 1 increases from 5% in pure diethyl ether to 84.5% in a 4.14 M lithium perchlorate-d
84 )(AsF(6))(0.50) have been prepared by adding diethyl ether to a dichloromethane solution containing e
85  procedure, the crude solids are washed with diethyl ether to afford the pure products, as revealed b
86             Thus, as the medium changes from diethyl ether to one containing ionic clusters of lithiu
87 ed silica gel column eluted with pentane and diethyl ether to separate minor compounds.
88                    Consequently, addition of diethyl ether to the reaction mixtures could precipitate
89   Addition of a silylated acetylide to 11 in diethyl ether/trimethylamine gave mainly 22a.
90                Liquid-liquid extraction with diethyl ether was followed by GC-MS for TCE quantificati
91 netic isotope effects for the reactions with diethyl ether were measured.
92 two intermediates with ethyl vinyl ether and diethyl ether were monitored by single- and double-mixin
93 Pr5)(2)Ln(2)I(4) (Ln = Y, Gd, Tb, Dy, Tm) in diethyl ether with potassium graphite in the presence of
94 anesthetics, such as chloroform, isoflurane, diethyl ether, xenon, and propofol, disrupt lipid rafts