ライフサイエンスコーパス: phenyl group

1 between the carbonyl oxygen and the flanking phenyl group.

2 o a diradical intermediate stabilized by the phenyl group.

3 erocycles, which can be either a methyl or a phenyl group.

4 s is attached to the para position of the 20-phenyl group.

5 ue to a conformational change of the pendant phenyl group.

6 orm the related o-benzyne through shift of a phenyl group.

7 aches the diene in an exo fashion syn to the phenyl group.

8 her remote from the 4'-position on the 3beta-phenyl group.

9 as resistant to nintedanib analogs lacking a phenyl group.

10 stability to the cyclopropenylium core as a phenyl group.

11 ha-carbon preceding functionalization of the phenyl group.

12 rporate a 4-hydroxy substituent on the omega-phenyl group.

13 r-95' are responsible for the binding of the phenyl group.

14 ctures, e.g., the two ester groups and the 6-phenyl group.

15 nd possible hydrophobic association with the phenyl group.

16 atoms in the 3'- or 4'-position of the free phenyl group.

17 ere the cyclohexyl group was replaced with a phenyl group.

18 e Ru atom is coordinated by the P atom and a phenyl group.

19 adentate pyridinophane ligand containing one phenyl group.

20 functionalizing the alpha-methyl over alpha-phenyl group.

21 ls 0 and 2) between the amide moiety and the phenyl group.

22 ties to ortho- or para-positions of the meso-phenyl groups.

23 with high regiocontrol on the ferrocenyl and phenyl groups.

24 op in SFG signal is also observed for the PS phenyl groups.

25 s oriented s-trans to both the isopropyl and phenyl groups.

26 e porphyrin; the other meso-substituents are phenyl groups.

27 t this is due to the basic properties of the phenyl groups.

28 a dimethyl amino or one of seven substituted phenyl groups.

29 FMN plus one phenyl group, and FMN plus two phenyl groups.

30 ural isomers which differ in the position of phenyl groups.

31 r rotors bearing three, five, six, and seven phenyl groups.

32 by proper substitution of its benzamido and phenyl groups.

33 ed to the installation of halogen, ester and phenyl groups.

34 to the ortho-positions of both adjacent meso-phenyl groups.

35 yl groups could bias the conformation of the phenyl groups.

36 -substituted with meta- and para-derivatized phenyl groups [(1S)-substituted 1, 4-dideoxy-1,4-imino-D

37 The introduction of a methyl (2b) or phenyl group (2c) on the 2'-position of 4'-imidazolyl ri

38 s are displaced along their long axes by one phenyl group (~4.3 A).

39 bon next to the carbene center is a nonbulky phenyl group, a variety of substitution patterns should

40 The addition of phenyl groups about the fulvene raised the reduction pot

41 ar the S1' subsite; substitutions off of the phenyl group accessed S1' and other distant binding regi

42 ic substitution of the ortho-position of the phenyl group adjacent to the oxime, forming a quinoline

43 group is cation-stabilizing relative to the phenyl group, albeit the 1,5 triazole is significantly d

44 olenine moiety, with either an n-propyl or a phenyl group alongside a methyl group, were synthesized

45 imal and that a p-hydroxyl group on the N(1)-phenyl group also enhances affinity and selectivity for

46 udied all have a weaker coupling between the phenyl group and a much weaker dependence of the molecul

47 -seven 2-phenylquinolines substituted at the phenyl group and C4 of the quinoline were synthesized an

48 N-acetyl-(d)-glucosamine bearing a 4-methoxy phenyl group and different amino acid esters on the phos

49 idine, metalation was initiated alpha to the phenyl group and led finally to a fused tricyclic adduct

50 Alterations of the phenyl group and of the oxalamide linker indicated that

51 t exclusively in a conformation in which the phenyl group and silicon atom are anti and the side chai

52 g in the axial or equatorial location of the phenyl group and the angle of rotation about the Si-CPh

53 nd the length of the alkyl chain between the phenyl group and the piperazine ring influenced binding

54 se from hydrophobic interactions between the phenyl group and the purine/pyrimidine site.

55 has a two methylene linker between the 3beta-phenyl group and the remote phenyl group, has an IC(50)

56 group, amplification of SERS signals by the phenyl group and thus shielding of the background noise

57 lity appended with a 3,5-bis(trifluoromethyl)phenyl group and was able to mediate transmembrane chlor

58 t pharmacophore groups, including phenol and phenyl groups and a hydrophobic moiety.

59 kephalin contains the interesting motions of phenyl groups and of side chains relative to the backbon

60 nificantly, we find that the presence of the phenyl groups and the NO ligand leads to substantial mix

61 r chiral recognition compared to that with a phenyl group, and an anion with an isobutyl group has th

62 eric compounds corresponding to FMN plus one phenyl group, and FMN plus two phenyl groups.

63 ows exclusive bond insertion to the adjacent phenyl group, and no evidence of Wolff rearrangement.

64 tion fragment resulting from the loss of the phenyl group, and this ion is not observed in the invers

65 Hydrazones bearing EDGs at the stator phenyl group are an exception and show up to 6 orders of

66 CF(3), 4-OCF(3), 4-SO(2)Me, and 4-Cl) at the phenyl group are well-tolerated, and small alkyl substit

67 ontaining para-trifluoromethyl, t-butyl, and phenyl groups are a novel class of peroxisome proliferat

68 Bonds that are trans to phenyl groups are longer (Ir-C av = 2.071 A, Ir-N av = 2

69 structure of 9a shows that the isopropyl and phenyl groups are mutually cis and that the tolyl moiety

70 roups opposite each other, whereas all three phenyl groups are opposite pyridyl or pyrazolyl groups i

71 d by water in the nanolog complexes, and the phenyl groups are organized in a manner that attempts to

72 the quinoxaline ring; quinoxaline pendants (phenyl groups) are found to favor helical arrangements i

73 ole, Asp(32) carboxylic acid, and C-terminal phenyl groups arrayed about a common backbone configurat

74 rties on the position of substituents on the phenyl groups as compared to those observed in substitut

75 e lower potency of 14 (beta-orientation of 8-phenyl group) as compared to 8a (alpha-orientation) was

76 rent linkers to a nucleobase, nucleoside, or phenyl group, as a side-chain extension at the C22 posit

77 -ene precursors incorporates either a 3-endo-phenyl group, as an acid precursor, or a 3-endo-phenyldi

78 oration of two fluorine atoms in the central phenyl group, as in 20 and 21, is extremely advantageous

79 fluorescent protein (GFP) chromophore with a phenyl group at C(2) of the imidazolone has been synthes

80 This effect may be profound: a 3,5-bis-CF3 phenyl group at C(5) in 1,3-dioxane displays a pronounce

81 Whereas one might expect an axial phenyl group at C(5) of 1,3-dioxane to adopt a conformat

82 of 2a with a 3-thiophene or an unsubstituted phenyl group at C-6 were the most potent inhibitors.

83 nyl group and a 4-[2-(trimethylsilyl)ethynyl]phenyl group at diametrically opposed beta-positions (2,

84 bination with a four-carbon chain carrying a phenyl group at position-3 and a linear propyl group at

85 enyl group or a 4-[2-(trimethylsilyl)ethynyl]phenyl group at the 12-position, and a 4-iodophenyl grou

86 The introduction of a bulky phenyl group at the 3'-position exerted a profound influ

87 When the furanones had a phenyl group at the 3-position (X(3)), alternative photo

88 Attachment of a phenyl group at the 4'-position of 6a or the equivalent

89 by changing the substituents attached to the phenyl group at the 4-position of the quinoline ring of

90 In contrast, the introduction of a phenyl group at the 5'-position of 6a did not cause any

91 quence allows for a facile introduction of a phenyl group at the ortho position of phenols and anilin

92 This demonstrates the ability of the phenyl group at the PS/PA-18 interface to rearrange itse

93 le rings or one indole ring and two aromatic phenyl groups at a fixed distance of six polyethylene gl

94 oration of heterocycles at the C-5 position, phenyl groups at C-4, and a variety of differently subst

95 methyl, isopropyl, tert-butyl, adamantyl, or phenyl groups at C5 is reported here, starting by coupli

96 n DAG-lactones with identical functionalized phenyl groups at either the sn-1 or sn-2 position are co

97 3,2-b]carbazole with differently substituted phenyl groups at nitrogen atoms is reported.

98 trical strap, attached to ortho positions of phenyl groups at opposing meso positions of the porphyri

99 pha]quinoxaline ureas containing substituted phenyl groups at the 3-position was developed.

100 The 3-(dimethylamino)phenyl groups at the alpha position prove to be importan

101 ns and para-substituted (Br, NO(2), ethynyl) phenyl groups at the C(10) and C(15) meso positions.

102 The indolenine precursors with a phenyl group attached at the chiral center were asymmetr

103 erfluorinated meso-phenylporphyrins with one phenyl group bearing a substituent in the ortho position

104 In the assembly of these molecules, the phenyl groups block the herringbone motif and further gu

105 bridge added between the position 5 and the phenyl group bound to the position 6 dramatically increa

106 wed to explain the axial predominance of the phenyl group by a larger polarization of the Si-Ph than

107 Bioisosteric replacement of the aromatic phenyl group by a thiophene moiety produced some of the

108 m via intramolecular metal-metal cooperative phenyl group C(sp(2))-H oxidative addition to the dinick

109 SAR studies of 1d showed that the 3-phenyl group can be replaced by a pyridyl group, and a s

110 The pendant phenyl group can be used to modify the intrinsic optoele

111 ctive C-center on these fluorine-substituted phenyl groups can be controlled by charge state.

112 ptical properties, where the introduction of phenyl groups caused a progressive red-shift and reducti

113 has a 3,5-dialkoxy substitution on the imide phenyl groups (CBI-35CH), leading to "molecular pockets"

114 ophobic substituent differs in length by one phenyl group compared to that of oritavancin, N'-4-[(4-c

115 tuents such as tert-butyl, compound 33, or a phenyl group, compound 29, resulted in inactive FPT inhi

116 Specific phenyl group conformations are shown to be critical to t

117 rphyrin), where the 2-position of one of the phenyl groups contains -NH(2), -N(CH(3))(2), and -N(CH(3

118 Waals interactions with mAb 2E2, whereas the phenyl group contributes to the binding primarily via hy

119 hiral surfaces lined with nitrate anions and phenyl groups create multiple binding sites for guest an

120 ondary alkyl, and acyl groups exchanged, but phenyl groups did not.

121 S protecting group can serve as an efficient phenyl group donor for o-bromophenols via Pd-catalyzed C

122 phenyltin efficiently transferred up to four phenyl groups during fluoride-promoted couplings with ar

123 catalyst bearing two 3,5-bis(trifluoromethyl)phenyl groups efficiently catalyzed diverse heterocycliz

124 e varied pairwise among the electron-neutral phenyl groups, electron-rich 4-(N,N-dimethylamino)phenyl

125 lucose of Globo H with the fluoro, azido, or phenyl group elicited IgG antibody response to specifica

126 Inclusion of a 6-phenyl group enhanced A3 receptor selectivity: Compound

127 ogen bond donors in the para position of the phenyl group enhanced NR1A/2B potency.

128 The phenyl groups feature substituents with increasing elect

129 chain length between N-1 of indole and the 2-phenyl group from n = 1 through n = 3 leads to a fairly

130 tructured N-terminal region, deletion of the phenyl group from Phe3 yielded a peptide that reduced bi

131 de to promote transfer of one, two, or three phenyl groups from the organogermanes.

132 ne films when vapor deposited, DPT's pendant phenyl groups frustrate crystal growth, yielding amorpho

133 een the exo N atom of the sugar moiety and a phenyl group furthermore increased the observed apparent

134 l ligand (2) consisting of a noncoordinating phenyl group gave only low molecular weight branched oli

135 phosphorus center, along with ferrocenyl and phenyl groups, generating phosphines of the general stru

136 opyridinyl (MPTP) analogues in which the C-4 phenyl group has been replaced with various 4-azaaryl mo

137 ion of 17a is anomalous, suggesting that the phenyl group has more than a simple steric effect.

138 hdrawing and -donating substituents on the 3-phenyl groups has been prepared and characterized.

139 etween the 3beta-phenyl group and the remote phenyl group, has an IC(50) value of 5.14 nM at the DAT.

140 rosulfanyl)phenyl and m-(pentafluorosulfanyl)phenyl groups have been characterized by low-temperature

141 Other substituents on the phenyl group, HS-Ph-X, where X = -F, -CH3, -OCH3, also s

142 ation of the acidities and the effect of the phenyl group in acetonitrile, and the position of the C=

143 e findings demonstrate the importance of the phenyl group in modulating the chaperoning efficacy and

144 clopentenones containing a 4-(methylsulfonyl)phenyl group in the 3-position and a phenyl ring in the

145 contrast, analogs of alpha-GalCer containing phenyl group in the lipid tail could neither induce NKT

146 ose to the alpha-carbon and the other with a phenyl group in the same location.

147 t of the antiviral potency by inclusion of a phenyl group in the side chain of these compounds.

148 fluences the position of the syn-pseudoaxial phenyl group in the TADDOL structure.

149 in of the dual emission was dependent on the phenyl group in the Z-isomer, which stabilizes the Franc

150 rates of the free rotation available to the phenyl groups in 2,4-diphenyl-1,3(Z)-pentadiene compared

151 03 (S)) analogues, containing 7- and N(6)-NH phenyl groups in 7-deazaadenine, robustly inhibited AdK

152 er family, consist of alternating alkene and phenyl groups in conjugation.

153 -Pylm, Ph-Pylm, and t-Bu-Pylm insert their 4-phenyl groups in either the CB[7] or CB[8] cavity.

154 The migratory aptitudes of the varied phenyl groups in rearrangement-displacements of 13 with

155 enabled by introduction of para-substituted phenyl groups in the equatorial (eq) dithiolene ligand a

156 The strong trans influence of the phenyl groups in the meridional isomers leads to the obs

157 udes six compounds bearing 2,5-disubstituted phenyl groups in the side chain (with little, if any, di

158 ared to the constraint to coplanarity of the phenyl groups in the title compound.

159 spectroscopy, demonstrating the presence of phenyl groups, indicative of the grafted layer as well a

160 important contacts with RNase A, whereas the phenyl group interacts with Ang.

161 to the oxy group and sandwiched between two phenyl groups involving a unique ...c.g.phenyl interacti

162 ersion of Au144 to Au99 occurs only when the phenyl group is directly attached to the thiol, suggesti

163 ed adenosines, A-3CPh and A-4CPh, in which a phenyl group is linked to the adenosine such that it may

164 As follows from QTAIM analysis, the phenyl group is more stable when it is located in the ax

165 l-6-oxoverdazyl radicals 1[n], in which each phenyl group is substituted with three alkylsulfanyl gro

166 miempirical MNDO calculations shows that the phenyl group is twisted 89 degrees from the plane of cen

167 -carbon-to-o-phenyl linkages to the flanking phenyl groups, is described.

168 The phenyl group itself is situated near the S1' subsite; su

169 introduction of an aminomethyl group on the phenyl group led to monomer X, which was found to therma

170 adenine binding pocket; however, none of the phenyl groups lie in the same position as adenine in S1d

171 from the omega-phenyl group to the benzyl or phenyl group located on the 4-position of the piperidine

172 ivatives, when bearing a 4-alkyl but not a 4-phenyl group, maintained affinity for adenosine receptor

173 *)/H) self-exchange reactions reveal why the phenyl groups make the last of these reactions several o

174 n step in which the substrate's carboxylated phenyl group makes a nucleophilic attack to form the pyr

175 dine-, and 2-quinoxaline-based olefins and a phenyl group nucleophile.

176 phenylcyclobutene, "outward" rotation of the phenyl group occurs exclusively.

177 substitution at the para position of the P1' phenyl group of 1 resulted in the identification of equi

178 Replacement of the 3-phenyl group of 29 with alternatives led to reduced affi

179 atom at the para position of the pendant 5'-phenyl group of 6c not only provided further improvement

180 elective Pt-catalyzed hydrogenation of the 5-phenyl group of a 4,5-diphenyloxazolidine under acidic c

181 t His102 interacts directly with the pendant phenyl group of diazepam, and further implications for t

182 a pendant phenyl moiety, analogous to the 5-phenyl group of flunitrazepam, which are proposed to ove

183 Both the hydroxyl group and phenyl group of HveA-Y23 contribute to HSV entry.

184 r nitrogen atom in the space occupied by the phenyl group of MPTP leads to a dramatic decrease in sub

185 The common halogenated phenyl group of nonpeptide ligands was a determinant of

186 tituted 1,2-dibenzamidobenzenes in which the phenyl group of one benzoyl group (A-ring) was substitut

187 e, 2-hydroxy-2,4-pentadienoate, in which the phenyl group of phenylenolpyruvate is replaced with a do

188 this study, analogues in which the terminal phenyl group of the dibemethin was replaced with a 2-pyr

189 drogen bonding distance to the 6-(p-hydroxy)-phenyl group of the excited coelenteramide is a likely c

190 ding pocket of CDK2, and the position of the phenyl group of the inhibitor enables the inhibitor to m

191 The effect of this chelation is to place the phenyl group of the inhibitor into the important S1 spec

192 en the C2-carbon of the carbohydrate and the phenyl group of the metal carbenoid, while pai/pai inter

193 ps such as methoxy, vinyl, or chloro and the phenyl group of the other benzoyl group (B-ring) was sub

194 yl (14) substituents in each position of the phenyl group of the phenylcarbamoyl moieties, and with N

195 dine analogue (1-NAP-lobelane), in which the phenyl groups of lobelane were replaced with 1-naphthyl

196 teractions with the piperazine, anilino, and phenyl groups of nintedanib, providing a structural basi

197 the detailed PCA analyses indicate that the phenyl groups of PS tended to move away from the surface

198 ne of the meso-phenyl groups, while the meso-phenyl groups of the third NCP (3) are substituted with

199 peptide acetals via nucleophilic attack of a phenyl group on an endocyclic acyliminium ion 4 was expl

200 s is highly affected by the existence of the phenyl group on the alkyne terminus.

201 Accordingly, a phenyl group on the asymmetric center in the homologated

202 ctivity, while substitution with a methyl or phenyl group on the chain was well tolerated.

203 he two peptide backbone substituents and the phenyl group on the cyclopropane rings in 7-9were specif

204 We also report the influence of the meso-phenyl group on the emission properties of the aggregate

205 dities of 1d and 1e, the large effect of the phenyl group on the gas-phase acidity of 1e, the strong

206 D)Cl]2 and P(OPh)3 by cyclometalation of the phenyl group on the ligand and have shown such species t

207 The cycloadducts with a 4-(dimethylamino)phenyl group on the maleimide nitrogen atom undergo retr

208 Pd atom placed at the opposite side to the 2-phenyl group on the nearest stereogenic center of the py

209 The introduction of a methyl of phenyl group on the nitrogen of the pyrazolyl ring of 14

210 used to explore the optimal location of the phenyl group on the side chains.

211 angement involving migration of the allyl or phenyl group on the silicon atom to the adjacent enone c

212 YNPHOS) containing 3,5-bis(trimethylgermanyl)phenyl groups on phosphorus and applied this ligand to t

213 nation interactions restrict the rotation of phenyl groups on tetraphenylethene units, these metallac

214 as the gamma-hydroxyl and the remaining two phenyl groups on the butenolide ring essentially orthogo

215 itro substituents as acceptor groups and two phenyl groups on the phenolate moiety.

216 figuration places strongly trans influencing phenyl groups opposite each other, whereas all three phe

217 through ortho-substitution on the benzyloxy phenyl group or through replacement of the ether oxygen

218 ning vicinal dimethyl groups and an adjacent phenyl group or trisubstituted alkene are exceptionally

219 hydride particles modified with immobilised phenyl groups or larger ligands followed trends predicte

220 gh stabilizing weak interactions between its phenyl group (or cyclohexyl group) and the carboxylate g

221 ents (H and CH3) were found to bind with the phenyl group oriented in the plane of the quinazoline ri

222 ors the enantiomorph containing a deuterated phenyl group over the protio or (13)C version, and the p

223 f the greater relative migratory aptitude of phenyl groups over alkyl groups, and provides an efficie

224 orpholino) were bound to the enzyme with the phenyl group perpendicular to the quinazoline ring and p

225 ion-based kinetic resolutions and a role the phenyl groups play in that selectivity.

226 e, but strict structural requirements at the phenyl group position of the unit A delta-hydroxy octadi

227 in the active site, with the pai-face of the phenyl group positioned over the heme iron atom.

228 differ only in the isotopic composition of a phenyl group positioned remote from the chiral center.

229 hanges in chain length or replacement of the phenyl group producing greatly decreased values of k(cat

230 enolic functionalities on two of the opposed phenyl groups prove to be remarkable catalysts for the r

231 (C6-C9)-acyl chains with a distal phenyl group proved to be the most potent inhibitors.

232 nal 2-pyridyl substituent and the acyl chain phenyl group provide key anchoring interactions and conf

233 eplacements or substituents for the terminal phenyl group provided effective inhibitors (e.g., 5c, ar

234 triazolyl alcohols 3h,i,k-m migration of the phenyl group rather than the corresponding heteroaromati

235 ing substituents at the para position of the phenyl group (RBpT).

236 dihydroxylated TPHP, RDP with the loss of a phenyl group (RDP-[Phe]) and RDP oligomers were detected

237 Mansyl probes, which have an extra phenyl group relative to dansyl, were found to locate de

238 Parallel theoretical calculations, with the phenyl groups replaced by methyl groups, yield informati

239 elling case for its broader application as a phenyl group replacement in scenarios where the aromatic

240 This established that the migrating phenyl group required an orientation facing the enone be

241 R2 and R5 positions of the 2,5-disubstituted phenyl group, respectively.

242 stituents at the 4-position of the central N-phenyl group resulted in compounds with improved potency

243 Replacing the 2-ethyl substituent with a phenyl group results in a compound that retains 5-HT(6)

244 Appropriate substitution of the phenyl group results in ligands with particularly high a

245 substituents on the para position of the C-2 phenyl group retained the activity of the initial analog

246 t an extension from the meta-position on the phenyl group (ring-5) would improve interactions with th

247 zene in search of evidence on the effects of phenyl group rotation and chromophore aggregation of oli

248 e analogs (BCNAs) with a p-alkyl-substituted phenyl group seem to require aromatic ring stacking inte

249 lene is stabilized more by a naphthyl than a phenyl group (singlets, 26.6 versus 24.4; and triplets,

250 methyl)phenyl or 3,5-bis(pentafluorosulfanyl)phenyl groups strongly suppresses the byproduct formatio

251 ed capsule is narrow, but still accommodates phenyl groups such as those presented by p-quaterphenyl

252 enylporphyrin (ZnTPP) with the 5 and 15 meso-phenyl groups tethered by a 1,4-phenylenebis(butyl-4-oxy

253 o the adenosine such that it may replace the phenyl group that is eliminated by the Phe56Ala mutation

254 ted state has two interchangeably equivalent phenyl groups that have different formal oxidation state

255 C, favoring the conformation having an axial phenyl group, that is in only modest agreement with the

256 Owing to the steric hindrance of the axle phenyl group, the threading of the guest was seen to occ

257 Analysis of the flipping modes of the mobile phenyl groups, their rotational rates, and transition te

258 aromatized whether on the pyridine or on the phenyl group through 1,3-dipolar cycloaddition (1,3-DC)

259 ficulties encountered in the conversion of a phenyl group to a carboxylic acid will be discussed.

260 metal catalyzed partial hydrogenation of the phenyl group to an enol ether.

261 tion of substituents around the NH group and phenyl group to improve the selectivity and potency of P

262 Complex 1 efficiently transfers its phenyl group to PhSiH3, with formation of Ph2SiH2 and [C

263 y substituent was transferred from the omega-phenyl group to the benzyl or phenyl group located on th

264 MgCl and related reagents with transfer of a phenyl group to the nitrido ligand.

265 is linked to the para-position of one ZnTPP phenyl group to yield ZnTPP-PDI2.

266 strate computationally that by shifting from phenyl groups to "space efficient" acetylene moieties as

267 ations of the phenyl or the para-substituted-phenyl groups to C-1 with displacement of chloride ion.

268 iol ligand (1) in the asymmetric addition of phenyl groups to cyclic alpha,beta-unsaturated ketones.

269 chloride is capable of delivering all of its phenyl groups to the product.

270 tached at the para positions of the PerPh(4) phenyl groups to yield PerPh(4)-NDI(4).

271 thylaniline is replaced by an isopropyl or a phenyl group, trisolvated monomers are formed instead of

272 Although phenyl groups turned out to provide significantly less s

273 ed trans-stilbene is distorted, with the two phenyl groups twisted, while the geometry of the excited

274 pounds corresponding to hydroxy-FMN plus one phenyl group, two apparently isomeric compounds correspo

275 n of the PP or SP with a 3,4-(methylenedioxy)phenyl group was also examined.

276 The classic 4-azido-3-iodo-phenyl group was appended to either the C-1 or C-5 posit

277 The 8-phenyl group was introduced by Grignard addition to keto

278 nsporter (VAChT), a heteroaromatic ring or a phenyl group was introduced into the carbonyl-containing

279 ortho positions of two trans-positioned meso-phenyl groups, was synthesized from (3,3'-diethyl-4,4'-d

280 Phenyl groups weaken binding when close to the amine but

281 Multiple organic acids containing phenyl groups were also greatly increased in the presenc

282 e substituent on the aldehyde from methyl to phenyl groups were investigated by comparison of the tra

283 ylsilylbractazonine through migration of the phenyl group, whereas treatment of thebaine with strong

284 the phenol side chains in the NPXY motifs to phenyl groups (which cannot be phosphorylated) has major

285 to the viscosity-dependent twisting of the 5-phenyl group, which gives access to the dark nonemissive

286 BD acceptor unit is substituted with a donor phenyl group, which increases the twisting of the TCBD u

287 ed by an oxalamide to a p-halide-substituted phenyl group, which target this site, specifically, a ca

288 or nitro (2) substituents on one of the meso-phenyl groups, while the meso-phenyl groups of the third

289 Replacement of the C-2 phenyl group with a 3,5-substituted thiophene led to imp

290 le moiety is linked by a 1,3-bis(aminomethyl)phenyl group with a 5-(2-aminoethyl)- (18) or a 5-(2-dim

291 awal and a van der Waal's interaction of the phenyl group with a hydrophobic surface at the mouth of

292 iperone and found that replacement of the N1-phenyl group with a methyl group only slightly decreased

293 a unique preference for migration of the cis-phenyl group with formation of bicyclo[3.1.0]hexanone ph

294 dramatically improved by substituting the 2-phenyl group with halogens in the meta position or by re

295 ethylene linker, (ii) replacing the terminal phenyl group with less lipophilic heterocycles, or (iii)

296 gauged as a function of substituents on the phenyl group with p-OH, p-OMe, p-H, p-CF3, p-CN, and p-N

297 lled the "meshes" of the nanoribbon, possess phenyl groups with decyloxy solubilizing chains on each

298 Phenyl groups with different substituents were used to c

299 lored as well as the effect of replacing the phenyl groups with larger aromatic rings, 1-naphthalene

300 s lead to low-spin complexes while the bulky phenyl group yields high-spin complexes.