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1 as was the subsequent enolization with Et3N (triethylamine).
2 HPLC with the presence of a volatile reagent-triethylamine.
3 f alcohols is Pd(OAc)(2) in combination with triethylamine.
4 p-adenosine 3', 5'-cyclic monophosphothioate triethylamine.
5 es in the presence of copper(II) acetate and triethylamine.
6 treated with triphenylphosphine, iodine, and triethylamine.
7 thyl)phenol (tBu(2)qsalH) in the presence of triethylamine.
8 ylimidazole intermediates with 5x amines and triethylamine.
9 a conditions, in the presence of TiCl(4) and triethylamine.
10 ve isoindoline-1,3-diones in the presence of triethylamine.
11  enhanced by a factor of ~4 upon addition of triethylamine.
12 ESI-MS) was observed relative to ammonia and triethylamine.
13 ding trans-5,6-bromohydrins by reaction with triethylamine.
14 idant in the presence of carboxylic acid and triethylamine.
15 orides with oximes in the presence of excess triethylamine.
16  cycle for the conversion of dinitrogen into triethylamine.
17 vealed no evidence of catalytic formation of triethylamine.
18 ly the simple reagents N-iodosuccinimide and triethylamine.
19 the mechanism of reaction in the presence of triethylamine.
20 ith CAPS, 15.2 % with carbonate, 19.3 % with triethylamine, 19.6 % with quinuclidine, and 18.1 % with
21                            The photolysis of triethylamine (1a) in the presence of carbon dioxide lea
22 d under mild conditions with the formic acid/triethylamine (5:2) system as the hydrogen source and pr
23                     We explore the effect of triethylamine, a sacrificial hole scavenger incorporated
24 ffected by addition of a simple base such as triethylamine: A complex chiral base was not necessary.
25      By employing an eluent containing 25 mM triethylamine acetate (pH 6.3) and a column temperature
26  ethanol, toluene, benzene, amomnia, dioxan, triethylamine, acetonitrile, formaldehyde, m-xylene, 2,2
27  by reaction with a diene in the presence of triethylamine afforded (4+3) cycloadducts in good to exc
28 oxylamines with trichloroacetyl chloride and triethylamine afforded 3-alkylbenzoxazolones generally i
29 loride and acyl chlorides in the presence of triethylamine afforded the target allenes via Wittig rea
30 ith electrophilic alkenes in the presence of triethylamine affording substituted 5-nitroisoxazoles is
31  H89 and Rp-3', 5'-cyclic monophosphothioate triethylamine also caused a large reduction (>70%) in Ca
32       Loss of ethyl groups in reactions with triethylamine also occur by displacement, but preferenti
33                                              Triethylamine and 1-methylimidazole were found to be sel
34                               A buffer (7 mM triethylamine and 3 mM ammonium formate)/methanol, 50:50
35 um molybdate, followed by precipitation with triethylamine and combustion of the precipitate to yield
36 )[(S,S)-Ts-DPEN] in a mixture of formic acid-triethylamine and dimethylformamide at 25 degrees C.
37 esolved as a sharp peak with the addition of triethylamine and formic acid modifiers to a chloroform/
38 ble to produce cross-linked products in both triethylamine and methanol, with a reactivity pattern si
39           In addition, we replace DIPEA with triethylamine and pyridine to validate the reaction mech
40 hese include: toluene, benzene, and styrene; triethylamine and related trialkylamines; pyrrolidine as
41 he neutral nucleophiles dimethyl sulfide and triethylamine and the bromination with Br(-).
42 carboxylic acid (1,4-BDC) in the presence of triethylamine and water at room temperature.
43 are agent surrogates representing the amine (triethylamine) and organophosphonate (diethyl methythiom
44 isted of 385mM hexafluoro-2-propanol, 14.5mM triethylamine, and 5% methanol (mobile phase A) and 385m
45 e A) and 385mM hexafluoro-2-propanol, 14.5mM triethylamine, and 90% methanol (mobile phase B).
46 sting of the sulfur dioxide surrogate DABSO, triethylamine, and a palladium(0) catalyst for effective
47 on by treatment with titanium tetrachloride, triethylamine, and a variety of aldehydes at 0 degrees C
48 ence of 1 equiv each of a triarylbismuthane, triethylamine, and copper(II) acetate affords the diaryl
49 commonly used basic additives (diethylamine, triethylamine, and isobutylamine) showing unmatched chro
50 yield by cyclization using ethylene bromide, triethylamine, and KI at 80 degrees C.
51 rom carboxylic acids, N,N'-diphenylthiourea, triethylamine, and primary alkyl halides is described.
52  step follows, in which fumaryl chloride and triethylamine are added dropwise to a solution of PEG in
53 tigated using phenanthroline as a ligand and triethylamine as a base.
54 noptimized overpotential of ca. 500 mV using triethylamine as a base.
55 e stoichiometrically necessary equivalent of triethylamine as a base.
56                                              Triethylamine as a hydrophobic solvent was switched to p
57 rrent electrolysis in an undivided cell with triethylamine as a terminal reductant.
58  chloride at 0 degree C with the addition of triethylamine as acid scavenger.
59 y was reduced from 35 to 22 when introducing triethylamine as IPR; however, improved separations were
60 e of T3P (a mild cyclodehydrating agent) and triethylamine as the base.
61 is(3-methyl-imidazolin-2-ylidene)borate) and triethylamine as well as N,N-dimethylaniline donors have
62 ld be produced by only two novel procedures: triethylamine-assisted periodate oxidation and acetolysi
63 ne of 2H-perfluoro-2-methyl-3-pentanone with triethylamine at elevated temperatures yields a methylen
64 ile phase of 0.05M SDS/12.5% 1-propanol/0.5% triethylamine at pH 3, running at 1mL/min under isocrati
65 carbatriphyrin(2.1.1) with PCl(3) in toluene/triethylamine at reflux for 1 h.
66 mide from 2-nitrobenzenesulfonohydrazide and triethylamine at room temperature.
67 odifluoroalkylation of olefins that utilizes triethylamine base as the terminal reductant.
68 S]PAPS was eluted by a step-wise gradient of triethylamine bicarbonate buffer (pH 7.5).
69     Cupric acetate is the copper source, and triethylamine buffer is used to prevent protodeboration;
70  phase of 0.05M SDS - 7.5% 1-propanol - 0.5% triethylamine buffered at pH 3, running through a C18 co
71 ction of phenol, acetic acid, and protonated triethylamine by electrogenerated iron(0) tetraphenylpor
72 p(3)) coupling between alpha-bromoesters and triethylamine capable of accessing building blocks with
73 drophobic solvent was switched to protonated triethylamine carbonate by CO(2) and used to extract dit
74 mino-tetrafluoropropyl esters in acetic acid/triethylamine catalyst solution or continuous flow of ca
75  understand high diastereoselectivity in the triethylamine catalyzed spirocyclization reaction.
76 syn-aldols in the dicyclohexylboron triflate/triethylamine (Chx(2)BOTf/Et(3)N)-mediated enolboration-
77 sitylene core, (2) B = benzene core, (3) C = triethylamine core, and (4) D = tri(2-hexanamido)ethylam
78  using three different catalysts/initiators (triethylamine, DBU, and dimethylphenylphosphine) in chlo
79           Under similar conditions, however, triethylamine did not elicit any detectable color change
80     Lithium hexamethyldisilazide (LiHMDS) in triethylamine (Et 3N)/toluene is shown to enolize acycli
81 hese salts were treated in the same pot with triethylamine (Et(3)N), leading to the selective formati
82 has been developed using a mild base such as triethylamine (Et(3)N).
83                                              Triethylamine (Et3N) mediates esterification reactions b
84 ates of p-substituted cinnamyl alcohols with triethylamine followed by trimethylsilyl triflate (TMSOT
85 with PCl(3) in a mixture of solvents toluene/triethylamine for 4 h.
86 nsfer hydrogenation of 11 in the presence of triethylamine/formic acid and Noyori's chiral ruthenium
87 hydrides form efficiently in dichloromethane/triethylamine from 1 equiv of the alcohol.
88 presence of anhydrous potassium carbonate or triethylamine give 2-substituted condensed ring oxazoles
89 of 1-butylamine > 1-propylamine > pyridine > triethylamine > ethylamine > methylamine > diethylamine
90 ylammonium nitrate-trifluoroacetic anhydride-triethylamine has been developed for the synthesis of 2-
91 struction of a benzofuran moiety mediated by triethylamine has been developed.
92 timized solvent conditions: isopropanol in a triethylamine/hexafluoroisopropanol mixture highly incre
93 competitive precipitation in the presence of triethylamine, high selectivity (up to 80%) for lutetium
94                     In the presence of added triethylamine, however, the octadecylphosphonate ligands
95 es, accomplished by solvent precipitation of triethylamine hydrobromide, enabled their regiospecific
96                       2-(4-Chlorophenylthio)-triethylamine hydrochloride (CPTA) enhanced lycopene acc
97 ) N-acyl-l-cysteines 8a-e in the presence of triethylamine in CH(3)CN-H(2)O (3:1), but (ii) S-acyl-l-
98 hosphapalladacycle complex as a catalyst and triethylamine in chloroform at -45 degrees C proceeded i
99 of the diiodofiprole with tritium, Pd/C, and triethylamine in ethyl acetate and afforded [(3)H]TDF wi
100 by the reaction of M(2+), TPyA, H(2)DBQ, and triethylamine in MeOH solution.
101  reaction of M(BF4)(2).6H2O, TPyA, H2CA, and triethylamine in MeOH solution.
102 henyl isocyanate and a catalytic quantity of triethylamine in the presence of furan afforded dihydrof
103 romatography (hexanes/ethyl acetate), dilute triethylamine in THF, and potassium fluoride in DMF.
104 on using LiHMDS in N,N-dimethylethylamine or triethylamine in toluene affords a 65:1 mixture of LiHMD
105 eration of thiourea intermediate followed by triethylamine induced intramolecular SN(Ar) displacement
106 alo-4-aminopyridines with acyl chlorides and triethylamine is described.
107    The presence of an auxiliary base such as triethylamine is required in order to drive the reaction
108                                   The use of triethylamine is the key to the separation of N-CH(2)F a
109 olizine products, and using acetic anhydride/triethylamine leads to indolizine products in good yield
110 e presence of the sacrificial electron donor triethylamine leads to the appearance of the reduced sen
111                We report both Stadis-450 and triethylamine mass spectra in octane and discuss issues
112         Triphenylphosphine or mesyl chloride/triethylamine-mediated deoxygenation afforded 2H-indazol
113 efficiency through 140-h exposure to a pH 10 triethylamine mobile phase at 50 degrees C.
114 s including toluene, N,N-dimethylethylamine, triethylamine, MTBE, THF, 1,2-dimethoxyethane (DME), dig
115 cleophilicities: n-butylamine, diethylamine, triethylamine, N-methylpyrrolidine, and trimethylamine.
116 loride (InCl(3)), benzyl alcohol (BnOH), and triethylamine (NEt(3)).
117 limidazole in the presence of a base such as triethylamine occurs with nucleophiles such as amines, p
118 in AQP4-null mice, with maximal responses to triethylamine of 0.80 +/- 0.07 vs. 0.28 +/- 0.03 mV.
119 nd exchange under modestly basic conditions (triethylamine) of a series of 2-methyl-substituted compo
120 excited state can be reductively quenched by triethylamine or 1,4-diazabicyclo[2.2.2]octane to produc
121   In the presence of a Bronsted base such as triethylamine or acetate, the kinetically preferred Mark
122                                Ionization of triethylamine or triphenylamine with the source results
123 ssisted tritylation with trityl chloride and triethylamine or with trityl alcohol and catalytic trifl
124 ia benzylic deprotonation in the presence of triethylamine paves the way for the 1,2-addition reactio
125 swelled PDMS the most were diisopropylamine, triethylamine, pentane, and xylenes.
126 vity of CAPS (pH 10.4), carbonate (pH 10.4), triethylamine (pH 11.2), quinuclidine (pH 11.5), and L-a
127 ernal standard was obtained in 500mmol.L(-1) triethylamine, pH 12.3.
128 enoxanthones with phosphorus oxychloride and triethylamine (POCl3/Et3N).
129 ize that the rate enhancement is a result of triethylamine possibly altering the energetics of the Cd
130  heating with benzotriazole, morpholine, and triethylamine, produce, in a one-pot reaction, alpha-ben
131 e delivers benzoimidazothiazetidine, whereas triethylamine promotes the formation of benzoimidazothia
132  of approximately 100 mum were prepared from triethylamine-quaternized-poly(vinylbenzyl chloride) cro
133                                              Triethylamine reacts with tetranitromethane to generate
134 undergo hole transfer with electron-donating triethylamines readily but not electron transfer with el
135  generated from di-n-butylboron triflate and triethylamine rearranged in good yields and high selecti
136 onation of the air-stable salts in situ with triethylamine releases the corresponding phosphines 1a a
137      Treatment of this complex with H(2) and triethylamine results in the formation of the Ni(0) comp
138 Rp-adenosine 3',5'-cyclic monophosphothioate triethylamine (Rp-cAMPS) before conditioning.
139 Rp-adenosine 3',5'-cyclic monophosphothioate triethylamine (Rp-cAMPs), none of which blocked evoked I
140                                       Adding triethylamine significantly improved conversions.
141  upgraded to 109:1 by crystallization of the triethylamine solvate 44 which was isolated in 54% yield
142 substrates, the more established formic acid/triethylamine system gives superior results.
143 sive secondary and tertiary amines including triethylamine (TEA) and dimethylethanolamine (DMAE).
144 graphy (IPRP) with a mobile phase containing triethylamine (TEA) and hexafluoro-2-propanol (HFIP).
145                                              Triethylamine (TEA) and triethanolamine (TEOA) are renow
146 arginine are 57 ng (330 pmol; 31 mM) and for triethylamine (TEA) are 9 ng (88 pmol; 11 mM).
147 ing of aryl triflates with aryl amines using triethylamine (TEA) as base.
148 rescein (Fl) as the photosensitizer (PS) and triethylamine (TEA) as the sacrificial electron donor, t
149 F) instrument, demonstrated the potential of triethylamine (TEA) for shifting the charge state patter
150 m) were tested and compared with ammonia and triethylamine (TEA) for the separation of selected organ
151 is(tetrafluoroborate) under mild conditions (triethylamine (TEA) or molecular sieves) easily led to t
152  was mixed with diethylmethylamine (DEMA) or triethylamine (TEA) through a T mixer coupled to a time-
153  latter route is enhanced by the addition of triethylamine (TEA) to the reaction medium and by increa
154 ted electron transfer (PET) between 1(+) and triethylamine (TEA) undergo subsequent reactions to gene
155                                              Triethylamine (TEA) was able to generate concentration-d
156 rradiation of P in acetonitrile (with 0.25 M triethylamine (TEA)) thus identified as P(-) (singly red
157 ing the desolvation gas with base vapor from triethylamine (TEA), the charge reduction effect can be
158 roved signal-to-noise ratio in comparison to triethylamine (TEA)-passivated Au TNPs.
159 red by the addition of a catalytic amount of triethylamine (TEA).
160 I) as an activating agent in the presence of triethylamine (TEA).
161 th amino acid ester salts in the presence of triethylamine (TEA).
162                           Incorporation of a triethylamine (TEA)/water modifier mixture provided dram
163 he photogenerated hole to the hole scavenger triethylamine (TEA); and transfer of the photogenerated
164                 We found that dimethylamine, triethylamine, tetraethylammonium, tetrabutylammonium, t
165                         On exposure of 11 to triethylamine, the indeno-fused quinolizinium salts 15 w
166 of the N-protecting group (see scheme; TEA = triethylamine, TMS = trimethylsilyl).
167 re produced by simply changing the base from triethylamine to 1,8-diazabicyclo[5.4.0]undec-7-ene.
168 nd to be readily cyclized in the presence of triethylamine to afford the resulting protected pyrrolid
169 Ph)(3) using HRh(dmpe)(2) in the presence of triethylamine to form Et(3)N-BH(3) in high yields.
170 itu with molecular iodine in the presence of triethylamine to give 2-amino-4H-1,3-benzoxazines, where
171  diphenylphosphoryl azide in the presence of triethylamine to yield cyclic (S) carbamate 2.
172 ield into 2-alkylindanones by treatment with triethylamine, to effect isomerization to the isomeric e
173 l to a salt form, which can be reverted upon triethylamine treatment.
174 on of the framework through an organic base (triethylamine) treatment.
175 oride (AgF), tetrabutylammonium fluoride and triethylamine trihydrofluoride (TREAT.HF), as the source
176  uses nucleophilic fluorine sources, such as triethylamine trihydrofluoride and KF.
177  added to the solution prior to ESI, such as triethylamine, trimethylamine oxide, and imidazole.
178 (bpy)3 2+ and tripropylamine, tributylamine, triethylamine, trimethylamine, or sodium oxalate encapsu
179                                              Triethylamine, tripropylamine, and tributylamine were fo
180 tation reaction using ammonium molybdate and triethylamine under low pH has been applied to gel-based
181 nium acetate) and bases (ammonium hydroxide, triethylamine) under most conditions.
182 onic acid using diphenyl phosphorazidate and triethylamine upon heating) with the appropriate alcohol
183                                              Triethylamine was observed to be most effective, yieldin
184 reactions at silica surfaces pretreated with triethylamine were conducted to investigate the influenc
185  chemoselectivity than the commonly employed triethylamine when reducing substrates with moderate ene
186 H(2)O (1) (L = 2,2',2' '-tris(dipicolylamino)triethylamine), with pyridyl and alkylamine coordination

 
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