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1                                              TBAF-promoted 1,2-eliminative desulfonylation and concom
2                                              TBAF-promoted arylation was extended into the other enol
3 and nitroalkenes in the presence of SbCl(3), TBAF, AcOH, and a catalytic amount of Pd(OAc)(2), in CH(
4 [3.2.0]hept-2-ene-7-ones (15), followed by a TBAF workup, results in a low-temperature anion-accelera
5 addition of equimolar amounts of SbCl(3) and TBAF is necessary for this reaction to proceed smoothly.
6                                    Water and TBAF act as the source for S=O bond formation and fluori
7 e with NCS (N-chlorosuccinimide), water, and TBAF in acetonitrile.
8 lution-processable small-anion salts such as TBAF as an n-dopant of organic conjugated polymers posse
9 fluorides with simple fluoride salts such as TBAF.
10 (1, 14, and 18) were treated with commercial TBAF in THF, giving the novel calixarenes 2, 15, and 19,
11 tes to 0.5 M tetra-n-butylammonium fluoride (TBAF) in THF results in the cleavage of their iminoether
12 atalyst with tetra-n-butylammonium fluoride (TBAF) or CsF.
13 tivation by two different methods, fluoride (TBAF) and silanolate (TMSOK).
14                 Tetrabutylammonium fluoride (TBAF) additive exerts a dramatic effect on the regiosele
15 complex between tetrabutylammonium fluoride (TBAF) and a silanol.
16 ble and soluble tetrabutylammonium fluoride (TBAF) is demonstrated as an efficient n-type dopant for
17 xide (DMSO) and tetrabutylammonium fluoride (TBAF) or N-methylimidazole (NMI).
18                 Tetrabutylammonium fluoride (TBAF) reacts with (halomethyl)diphenyl(para-substituted-
19 zirine (5) with tetrabutylammonium fluoride (TBAF) under matrix-isolation conditions affords chlorofl
20 THF solution of tetrabutylammonium fluoride (TBAF) yielded polyfunctionalized (2E,4E)-4-carbinol alka
21 c activation by tetrabutylammonium fluoride (TBAF).
22                                  When X = H, TBAF deprotection of the silyl group yields H(2)C=C=CFP(
23 mines are found more efficient under milder, TBAF-mediated aryne formation at room temperature.
24               Doping of ClBDPPV with 25 mol% TBAF boosts electrical conductivity to up to 0.62 S cm(-
25 g with cyanide led to the discovery of a new TBAF-mediated isomerization of a 1,4-diene to a 1,3-dien
26    The use of a semistoichiometric amount of TBAF (protocol P1) provided the corresponding beta-hydro
27 ernatively, the use of a catalytic amount of TBAF led to a mixture of beta-hydroxy- and beta-silyloxy
28              The inverse order dependence of TBAF at high concentration is consistent with a pathway
29                    This remarkable effect of TBAF can be rationalized in terms of a deprotonation of
30 methylsilane were oxidized with a mixture of TBAF/KHCO(3)/H(2)O(2) in 71-98% yield.
31 e and other simple arenes in the presence of TBAF in DMF without the necessity of adding any ligands
32 e of these 1,4-oxazepanes in the presence of TBAF provided a 4-oxa-1-azabicyclo[4.1.0]heptane core.
33                           In the presence of TBAF, there was only a modest steric effect (except for
34  by stoichiometric Lewis bases (K(2)CO(3) or TBAF), to produce a mixture of Michael addition (M) and
35 lyl)aryl triflates in the presence of CsF or TBAF at room temperature provides a very direct, efficie
36  simple additives such as K2CO3, KOH, KF, or TBAF and with commercially available Pd/C as precatalyst
37 atalyzed C-H arylation followed by a routine TBAF deprotection of the resulting silacycles.
38 asked phenoxide nucleophiles in a subsequent TBAF-induced one-pot deprotection-cyclization step of th
39 se dienes are reported as well as subsequent TBAF-assisted/Pd-catalyzed Hiyama cross-coupling reactio
40 uenched with aqueous bicarbonate rather than TBAF.
41                                          The TBAF-catalyzed VMMR afforded high anti-diastereoselectiv
42                                          The TBAF-promoted coupling also occurs efficiently with elec
43 -3-N-methyl-5-iodouracil did not undergo the TBAF-promoted couplings with arenes or heteroarenes sugg
44 e and the sensitivity of the 5'-conjugate to TBAF further exemplify the usefulness of this nucleoside
45 the corresponding alkylidenephthalides under TBAF conditions.
46 inally, deprotection of 7 was achieved using TBAF and produced 8 in 97% yield.
47 s 3-fluoro-3-hydroxymethyloxindoles, whereas TBAF-mediated fluoride addition at the primary sp(3)-C c
48                         Treatment of 30 with TBAF/THF gave the O-tyrosine ethers 31 and 32 (1:1), whi
49 grees, cyclohexane) reacts with CsF and with TBAF in THF to give benzylfluoromethyl-1-naphthylsilane
50 oxasiline followed by protodesilylation with TBAF in DMSO.
51          The SEM group could be removed with TBAF or HCl.
52 steps, the resin is deprotected in situ with TBAF and coupled to the 3-bromo-5-iodo arene using the i
53 e SEM group can be removed by treatment with TBAF in THF or aqueous HCl in EtOH.
54  left essentially intact upon treatment with TBAF.
55                                  Workup with TBAF affords the anti-cyclopropyl alcohols in one pot in
56 this reaction, as in dichloromethane without TBAF the 2,7-diamino isomer was formed regioselectively,
57 r was formed regioselectively, while without TBAF the 2,3-diamino isomer was formed exclusively.