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1 ld nanoparticles (AuNPs) functionalized with thiophenol.
2 acetal center in the presence of Me2BBr and thiophenol.
3 ating electric fields on the SERS spectra of thiophenol.
4 ta-thujone when the radicals are quenched by thiophenol.
5 of the TBS-protected bicyclic ketone 7 with thiophenol.
6 protonation of the photochemically generated thiophenol.
7 iolate ligand derived from 2-(mercaptomethyl)thiophenol, 1,2-ethanedithiol, 1,3-propanedithiol, 1,3-b
8 ddition of N-heterocycle 1a onto alkyne over thiophenol 7 and phenol 8 is supported by control experi
9 ith 3, 7, and 7.2 Li/mol of compound to give thiophenol (74%), adamantamine (91%), and 1-adamantane m
11 of both [1 + 1] glycosylation reactions with thiophenol aglycone containing galactose acceptors, as w
12 ptional substrate versatility, accommodating thiophenols, alcohols, heterocyclic amines, as well as N
13 ctions of 9 with sulfur nucleophiles such as thiophenol allowed rapid assembly of thioether analogues
14 ize thiophenoxyacetic acid (TPAA) to produce thiophenol, allowing the development of a continuous spe
15 lyzed hydrolysis for a series of substituted thiophenol analogues were 10(2)-10(3)-fold smaller than
17 omotes the rapid and efficient reaction of a thiophenol and aryl or heteroaryl halide using a copper
19 bis(3-amino-1-hydroxybenzyl)diselenide using thiophenol and hydrogen peroxide was proposed involving
20 r-soluble triazole relative are catalyzed by thiophenol and tert-dodecanethiol [C(9)H(19)C(CH(3))(2)S
21 reoselective beta-addition products from the thiophenol and thioethanol conjugate addition reaction o
23 en synthesized in good isolated yields using thiophenols and fluorine-containing alpha,beta-unsaturat
24 synthesized by directed ortho-lithiation of thiophenols and phenols and by side-chain lithiation of
27 nucleophiles such as benzoic acids, phenols, thiophenol, and secondary sulfonamide also provide the d
28 ivity is high with most 1 degrees thiols and thiophenols, and a range of substituted dichloropyrimidi
30 gen bond donor on a scale similar to that of thiophenol, aniline, and amine groups but not as that of
31 ntly, the thiol-Michael reaction between the thiophenol anion and electron deficient alkynes/alkenes
32 ntriguingly, in these materials both HDA and thiophenol are observed to selectively bind to specific
33 urally similar compounds such as anilines or thiophenols are sporadically analyzed despite their radi
34 yl-10-methylacridinium tetrafluoroborate and thiophenol as a hydrogen-atom donor furnished the nitrog
35 fraction signals in the photodissociation of thiophenol as it passes through two conical intersection
36 or acceptor pair between phenylacetylene and thiophenol as the light-absorbing system to obviate the
38 ll 1,3-benzoselenazoles was assessed using a thiophenol assay, exhibiting greater antioxidant activit
41 g leaving groups such as esters, phenols, or thiophenols at the propargylic site eliminate and thus r
42 phenol, 4-methylphenol, 4-fluorophenol, and thiophenol, at many UV wavelengths (lambda(phot)), have
43 s used to date have been either a mixture of thiophenol/benzyl mercaptan, or the alkanethiol MESNA.
44 study of the dehydrogenation of substituted thiophenols by controlled charge injection from the tip
45 electron, and proton transfer events with a thiophenol cocatalyst furnish the product and regenerate
47 ogen atom abstraction by benzyl radical from thiophenol (DeltaH(++) = 3.62 +/- 0.43 kcal/mol, DeltaS(
48 n of phenylboronic acids and dimerization of thiophenol demonstrate the capabilities and advantages o
50 ly homolyzed via PCET in the presence of the thiophenol, despite a large difference in bond dissociat
51 elenocyanation of NH-free 7-azaindoles using thiophenols, diselenides, potassium thiocyanates, and se
52 Here, cooperative reactivity enhancements of thiophenol/disulfide mixtures reveal the importance of H
53 termolecular Michael addition/lactamization, thiophenol elimination, and N- to O-sulfonyl migration,
54 -(2-haloaryl)-3-alkyl-N-tosylaziridines with thiophenol, followed by copper powder-mediated intramole
55 eacts with a variety of indole analogues and thiophenol for diastereoselective C-C, C-N, and C-S bond
59 ptoethanol, glutathione, dithiothreitol, and thiophenol function with approximately equal efficiency
60 us carbamates upon radical cyclization using thiophenol gave substituted pyrroles as against dihydrop
62 investigated at different concentrations of thiophenol, H(2)O(2), and 1,3-benzoselenazoles as cataly
63 A ((+/-)-4-[2-(1-methyl-2-pyrrolidinyl)ethyl]thiophenol HCl) is a neuronal nicotinic acetylcholine re
64 need for the toxic mercury salts and pungent thiophenol historically used in methods aimed at prepari
66 e pKa of the departing substituted phenol or thiophenol in either a diethyl phosphate or a diethyl th
67 example is Knowles's acceleration effect of thiophenol in proton-coupled electron transfer mediated
68 idinones or prolinols, in combination with a thiophenol, iridium photoredox catalyst and visible ligh
70 by sec-phenethyl alcohol, PhC*(OH)CH3, from thiophenol, log(k(abs)/M(-1) s(-1)) = (8.88 +/- 0.24) -
72 d from showcase resonant dye and nonresonant thiophenol monolayers adsorbed on Au single crystals sug
73 that a small molecule, (2-morpholinobutyl)-4-thiophenol (MoTP), specifically ablates zebrafish larval
74 and practical catalyst was (4-carboxylmethyl)thiophenol ('MPAA'), a nonmalodorous, water-soluble thio
78 h appropriately substituted N-methylaniline, thiophenols, or 4-(N-methylamino)benzoyl-L-glutamate.
79 2) operates on a common catalytic cycle with thiophenol (PhSH) by way of photolytic cleaveage of the
81 ysis of 7b in the presence of ferrous ion or thiophenol produces good yields of dA, whereas less reac
82 vibrations of the model compounds indole and thiophenol report quantitatively on the electric fields
83 and by side-chain lithiation of substituted thiophenols, respectively, in one-pot by reacting with N
84 e deamination process to include phenols and thiophenols, resulting in the discovery of a new branch
85 s the detector probe; addition of *NO to the thiophenol ring of AuNPs@4-HTP was followed by autoxidat
86 on (HETCOR) experiments provide evidence for thiophenol selectively binding at surface vacancies.
90 batch and continuous flow regimes, involving thiophenols/thiols and enol-acetates to yield alpha-sulf
93 Ketyl radical V was competitively trapped by thiophenol to yield PhCH(OH)CH2OPh in competition with b
94 a process for the conversion of phenols and thiophenols to their difluoromethoxy and difluorothiomet
95 reacted with a second nucleophile (azide or thiophenol) to give the corresponding difunctionalized a
98 s with a cyclic distonic radical cation, and thiophenol trapping gives acyclic product 10 and cyclic
100 alkyne containing a nosylamide followed by a thiophenol treatment in basic conditions that triggers n
101 s are functionalized with terminal protected thiophenol units for attachment to metal surfaces (compo
102 boxylic acid (H4DOBDC) have been replaced by thiophenol units, led to the isolation of Mn2(DSBDC), a
103 e Newman-Kwart rearrangement of phenols into thiophenols were investigated in relation to the bulkine
104 ible light-induced rearrangement affording a thiophenol which rapidly undergoes thiol-Michael additio