ライフサイエンスコーパス: triethylamine

1 as was the subsequent enolization with Et3N (triethylamine).

2 p-adenosine 3', 5'-cyclic monophosphothioate triethylamine.

3 es in the presence of copper(II) acetate and triethylamine.

4 ding trans-5,6-bromohydrins by reaction with triethylamine.

5 idant in the presence of carboxylic acid and triethylamine.

6 orides with oximes in the presence of excess triethylamine.

7 cycle for the conversion of dinitrogen into triethylamine.

8 vealed no evidence of catalytic formation of triethylamine.

9 ly the simple reagents N-iodosuccinimide and triethylamine.

10 the mechanism of reaction in the presence of triethylamine.

11 HPLC with the presence of a volatile reagent-triethylamine.

12 f alcohols is Pd(OAc)(2) in combination with triethylamine.

13 The photolysis of triethylamine (1a) in the presence of carbon dioxide lea

14 d under mild conditions with the formic acid/triethylamine (5:2) system as the hydrogen source and pr

15 ffected by addition of a simple base such as triethylamine: A complex chiral base was not necessary.

16 ethanol, toluene, benzene, amomnia, dioxan, triethylamine, acetonitrile, formaldehyde, m-xylene, 2,2

17 by reaction with a diene in the presence of triethylamine afforded (4+3) cycloadducts in good to exc

18 oxylamines with trichloroacetyl chloride and triethylamine afforded 3-alkylbenzoxazolones generally i

19 loride and acyl chlorides in the presence of triethylamine afforded the target allenes via Wittig rea

20 H89 and Rp-3', 5'-cyclic monophosphothioate triethylamine also caused a large reduction (>70%) in Ca

21 Loss of ethyl groups in reactions with triethylamine also occur by displacement, but preferenti

22 Triethylamine and 1-methylimidazole were found to be sel

23 A buffer (7 mM triethylamine and 3 mM ammonium formate)/methanol, 50:50

24 um molybdate, followed by precipitation with triethylamine and combustion of the precipitate to yield

25 esolved as a sharp peak with the addition of triethylamine and formic acid modifiers to a chloroform/

26 ble to produce cross-linked products in both triethylamine and methanol, with a reactivity pattern si

27 he neutral nucleophiles dimethyl sulfide and triethylamine and the bromination with Br(-).

28 are agent surrogates representing the amine (triethylamine) and organophosphonate (diethyl methythiom

29 isted of 385mM hexafluoro-2-propanol, 14.5mM triethylamine, and 5% methanol (mobile phase A) and 385m

30 e A) and 385mM hexafluoro-2-propanol, 14.5mM triethylamine, and 90% methanol (mobile phase B).

31 sting of the sulfur dioxide surrogate DABSO, triethylamine, and a palladium(0) catalyst for effective

32 on by treatment with titanium tetrachloride, triethylamine, and a variety of aldehydes at 0 degrees C

33 ence of 1 equiv each of a triarylbismuthane, triethylamine, and copper(II) acetate affords the diaryl

34 yield by cyclization using ethylene bromide, triethylamine, and KI at 80 degrees C.

35 rom carboxylic acids, N,N'-diphenylthiourea, triethylamine, and primary alkyl halides is described.

36 step follows, in which fumaryl chloride and triethylamine are added dropwise to a solution of PEG in

37 noptimized overpotential of ca. 500 mV using triethylamine as a base.

38 e stoichiometrically necessary equivalent of triethylamine as a base.

39 chloride at 0 degree C with the addition of triethylamine as acid scavenger.

40 ld be produced by only two novel procedures: triethylamine-assisted periodate oxidation and acetolysi

41 ne of 2H-perfluoro-2-methyl-3-pentanone with triethylamine at elevated temperatures yields a methylen

42 ile phase of 0.05M SDS/12.5% 1-propanol/0.5% triethylamine at pH 3, running at 1mL/min under isocrati

43 mide from 2-nitrobenzenesulfonohydrazide and triethylamine at room temperature.

44 S]PAPS was eluted by a step-wise gradient of triethylamine bicarbonate buffer (pH 7.5).

45 Cupric acetate is the copper source, and triethylamine buffer is used to prevent protodeboration;

46 phase of 0.05M SDS - 7.5% 1-propanol - 0.5% triethylamine buffered at pH 3, running through a C18 co

47 ction of phenol, acetic acid, and protonated triethylamine by electrogenerated iron(0) tetraphenylpor

48 mino-tetrafluoropropyl esters in acetic acid/triethylamine catalyst solution or continuous flow of ca

49 sitylene core, (2) B = benzene core, (3) C = triethylamine core, and (4) D = tri(2-hexanamido)ethylam

50 using three different catalysts/initiators (triethylamine, DBU, and dimethylphenylphosphine) in chlo

51 Under similar conditions, however, triethylamine did not elicit any detectable color change

52 Lithium hexamethyldisilazide (LiHMDS) in triethylamine (Et 3N)/toluene is shown to enolize acycli

53 Triethylamine (Et3N) mediates esterification reactions b

54 ates of p-substituted cinnamyl alcohols with triethylamine followed by trimethylsilyl triflate (TMSOT

55 nsfer hydrogenation of 11 in the presence of triethylamine/formic acid and Noyori's chiral ruthenium

56 hydrides form efficiently in dichloromethane/triethylamine from 1 equiv of the alcohol.

57 presence of anhydrous potassium carbonate or triethylamine give 2-substituted condensed ring oxazoles

58 of 1-butylamine > 1-propylamine > pyridine > triethylamine > ethylamine > methylamine > diethylamine

59 ylammonium nitrate-trifluoroacetic anhydride-triethylamine has been developed for the synthesis of 2-

60 struction of a benzofuran moiety mediated by triethylamine has been developed.

61 timized solvent conditions: isopropanol in a triethylamine/hexafluoroisopropanol mixture highly incre

62 In the presence of added triethylamine, however, the octadecylphosphonate ligands

63 es, accomplished by solvent precipitation of triethylamine hydrobromide, enabled their regiospecific

64 2-(4-Chlorophenylthio)-triethylamine hydrochloride (CPTA) enhanced lycopene acc

65 ) 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-

66 hosphapalladacycle complex as a catalyst and triethylamine in chloroform at -45 degrees C proceeded i

67 of the diiodofiprole with tritium, Pd/C, and triethylamine in ethyl acetate and afforded [(3)H]TDF wi

68 by the reaction of M(2+), TPyA, H(2)DBQ, and triethylamine in MeOH solution.

69 reaction of M(BF4)(2).6H2O, TPyA, H2CA, and triethylamine in MeOH solution.

70 henyl isocyanate and a catalytic quantity of triethylamine in the presence of furan afforded dihydrof

71 romatography (hexanes/ethyl acetate), dilute triethylamine in THF, and potassium fluoride in DMF.

72 on using LiHMDS in N,N-dimethylethylamine or triethylamine in toluene affords a 65:1 mixture of LiHMD

73 alo-4-aminopyridines with acyl chlorides and triethylamine is described.

74 The presence of an auxiliary base such as triethylamine is required in order to drive the reaction

75 olizine products, and using acetic anhydride/triethylamine leads to indolizine products in good yield

76 e presence of the sacrificial electron donor triethylamine leads to the appearance of the reduced sen

77 We report both Stadis-450 and triethylamine mass spectra in octane and discuss issues

78 Triphenylphosphine or mesyl chloride/triethylamine-mediated deoxygenation afforded 2H-indazol

79 efficiency through 140-h exposure to a pH 10 triethylamine mobile phase at 50 degrees C.

80 cleophilicities: n-butylamine, diethylamine, triethylamine, N-methylpyrrolidine, and trimethylamine.

81 loride (InCl(3)), benzyl alcohol (BnOH), and triethylamine (NEt(3)).

82 limidazole in the presence of a base such as triethylamine occurs with nucleophiles such as amines, p

83 in AQP4-null mice, with maximal responses to triethylamine of 0.80 +/- 0.07 vs. 0.28 +/- 0.03 mV.

84 nd exchange under modestly basic conditions (triethylamine) of a series of 2-methyl-substituted compo

85 excited state can be reductively quenched by triethylamine or 1,4-diazabicyclo[2.2.2]octane to produc

86 In the presence of a Bronsted base such as triethylamine or acetate, the kinetically preferred Mark

87 Ionization of triethylamine or triphenylamine with the source results

88 ssisted tritylation with trityl chloride and triethylamine or with trityl alcohol and catalytic trifl

89 swelled PDMS the most were diisopropylamine, triethylamine, pentane, and xylenes.

90 ernal standard was obtained in 500mmol.L(-1) triethylamine, pH 12.3.

91 enoxanthones with phosphorus oxychloride and triethylamine (POCl3/Et3N).

92 heating with benzotriazole, morpholine, and triethylamine, produce, in a one-pot reaction, alpha-ben

93 e delivers benzoimidazothiazetidine, whereas triethylamine promotes the formation of benzoimidazothia

94 of approximately 100 mum were prepared from triethylamine-quaternized-poly(vinylbenzyl chloride) cro

95 onation of the air-stable salts in situ with triethylamine releases the corresponding phosphines 1a a

96 Treatment of this complex with H(2) and triethylamine results in the formation of the Ni(0) comp

97 Rp-adenosine 3',5'-cyclic monophosphothioate triethylamine (Rp-cAMPS) before conditioning.

98 Rp-adenosine 3',5'-cyclic monophosphothioate triethylamine (Rp-cAMPs), none of which blocked evoked I

99 Adding triethylamine significantly improved conversions.

100 upgraded to 109:1 by crystallization of the triethylamine solvate 44 which was isolated in 54% yield

101 substrates, the more established formic acid/triethylamine system gives superior results.

102 arginine are 57 ng (330 pmol; 31 mM) and for triethylamine (TEA) are 9 ng (88 pmol; 11 mM).

103 rescein (Fl) as the photosensitizer (PS) and triethylamine (TEA) as the sacrificial electron donor, t

104 F) instrument, demonstrated the potential of triethylamine (TEA) for shifting the charge state patter

105 is(tetrafluoroborate) under mild conditions (triethylamine (TEA) or molecular sieves) easily led to t

106 was mixed with diethylmethylamine (DEMA) or triethylamine (TEA) through a T mixer coupled to a time-

107 latter route is enhanced by the addition of triethylamine (TEA) to the reaction medium and by increa

108 Triethylamine (TEA) was able to generate concentration-d

109 rradiation of P in acetonitrile (with 0.25 M triethylamine (TEA)) thus identified as P(-) (singly red

110 th amino acid ester salts in the presence of triethylamine (TEA).

111 Incorporation of a triethylamine (TEA)/water modifier mixture provided dram

112 We found that dimethylamine, triethylamine, tetraethylammonium, tetrabutylammonium, t

113 On exposure of 11 to triethylamine, the indeno-fused quinolizinium salts 15 w

114 of the N-protecting group (see scheme; TEA = triethylamine, TMS = trimethylsilyl).

115 re produced by simply changing the base from triethylamine to 1,8-diazabicyclo[5.4.0]undec-7-ene.

116 nd to be readily cyclized in the presence of triethylamine to afford the resulting protected pyrrolid

117 Ph)(3) using HRh(dmpe)(2) in the presence of triethylamine to form Et(3)N-BH(3) in high yields.

118 diphenylphosphoryl azide in the presence of triethylamine to yield cyclic (S) carbamate 2.

119 ield into 2-alkylindanones by treatment with triethylamine, to effect isomerization to the isomeric e

120 oride (AgF), tetrabutylammonium fluoride and triethylamine trihydrofluoride (TREAT.HF), as the source

121 uses nucleophilic fluorine sources, such as triethylamine trihydrofluoride and KF.

122 (bpy)3 2+ and tripropylamine, tributylamine, triethylamine, trimethylamine, or sodium oxalate encapsu

123 Triethylamine, tripropylamine, and tributylamine were fo

124 tation reaction using ammonium molybdate and triethylamine under low pH has been applied to gel-based

125 nium acetate) and bases (ammonium hydroxide, triethylamine) under most conditions.

126 onic acid using diphenyl phosphorazidate and triethylamine upon heating) with the appropriate alcohol

127 Triethylamine was observed to be most effective, yieldin

128 reactions at silica surfaces pretreated with triethylamine were conducted to investigate the influenc

129 H(2)O (1) (L = 2,2',2' '-tris(dipicolylamino)triethylamine), with pyridyl and alkylamine coordination