ライフサイエンスコーパス: stilbene

1 es, 2 dihydrochalcones, 4 flavan-3-ols and 2 stilbenes).

2 YL(3) giving the highest selectivity for (E)-stilbene.

3 estigation of health-related effects of this stilbene.

4 rogenation of diphenylacetylene (DPA) to (E)-stilbene.

5 ene, whereas C(3)G3 and C(2)G3 gave only cis-stilbene.

6 absorption spectrum blue-shifted from trans-stilbene.

7 functionalization of all eight corners with stilbene.

8 ion lifetimes compared to solutions of trans-stilbene.

9 f the second C-N bond accounts for the trans-stilbene.

10 red elimination of NO and formation of trans-stilbene.

11 ovel G4-binding chemotype derived from stiff-stilbene.

12 e, and a cationic donor-acceptor substituted stilbene.

13 ons, 7 phenolic acids, 6 flavan-3-ols, and 1 stilbene.

14 hen samples are expected to contain only one stilbene.

15 n converted to a new analogue of the natural stilbene.

16 iginal NHC-stabilized 1-silaketene 4 and cis-stilbene.

17 ew route to the stereoselective synthesis of stilbenes.

18 en developed in order to form functionalized stilbenes.

19 ariation in genotypes that do not accumulate stilbenes.

20 flavonols, flavan-3-ols, phenolic acids, and stilbenes.

21 at are formed from the end-to-end linking of stilbenes.

22 m ions are reported from sterically hindered stilbene 1,1'-bi(benzocyclobutenylidene) 1, its dimethox

23 Reactions of hindered stilbenes 1 and 5 with Br 2/CDCl 3 were examined via NMR

24 llustrate our method by showing that E stiff stilbene (1,1'-Delta-biindan) with up to 700 pN of force

25 and Ca(2+)-dependent, 4,4'-diisothiocyanato-stilbene-2,2'-disulfonic acid (DIDS)-sensitive and gluco

26 l cells; and (iii) the 4,4'-diisothiocyanato-stilbene-2,2'-disulfonic acid (DIDS)-sensitive and Na(+)

27 benclamide, but not by 4,4'-diisothiocyanato-stilbene-2,2'-disulfonic acid (DIDS).

28 ility of 4-acetamido-4'-((iodoacetyl) amino) stilbene-2,2'-disulfonic acid, disodium salt (IASD), to

29 that NCBE mediates the 4,4'-diisothiocyanato-stilbene-2,2'-disulfonic acid-sensitive, Na(+)-dependent

30 le is the 1:1 charge-transfer complex trans--stilbene-2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodime

31 in, 3-deoxyschweinfurthin B-like p-nitro-bis-stilbene (3dSB-PNBS), which displays biological activity

32 in the acute infection mouse model, just one stilbene (6-fold) and two pyridine-containing acetylene

33 whether resveratrol (3,5,4'-trihydroxy-trans-stilbene), a phytoalexin found in red grapes and blueber

34 We investigated stilbenes, a group of phenolic compounds found in Norway

35 tion rate between stilbene donor (Sd(+)) and stilbene acceptor (Sa(-)) linkers separated by AT bridge

36 istinguished the behavior of genotypes, with stilbene accumulation as the major metabolic event, alth

37 This stilbene also potentiated the apoptotic effects of borte

38 lectively binds the trans isoform of a stiff-stilbene (amino-tSS)-a rapidly and reversibly photoisome

39 ic zinc carboxylate vertices joined by trans-stilbene, analogous to the isoreticular MOF (IRMOF) seri

40 Piceatannol, a stilbene analogue to resveratrol with higher antioxidant

41 We find that isomerization of these stilbene analogues is little effected by the presence of

42 ficient synthesis of hydroxyl-functionalized stilbene and 2-arylbenzo[b]furan derivatives and report

43 d in vitro and in vivo: 3,4'-dihydroxy-trans-stilbene and 3,4'-dihydroxybibenzyl (lunularin).

44 harge-transfer excited complex of an anionic stilbene and a cationic, parallel pi-stacked tryptophan.

45 quinones, a furanochromone, an isoflavone, a stilbene and an iridoid).

46 were found to afford higher solubilities of stilbene and azobenzene.

47 re probed through geometric isomerization of stilbene and azobenzene.

48 (50) = 11.5 muM), or an equimolar mixture of stilbene and chalcone (IC(50) = 32.5 muM) were less pote

49 Of the 92 stilbene and dihydrostilbene analogues synthesized, near

50 on oxidation of E-4,4'-bis[di(p-anisyl)amino]stilbene and E,E-2,5-bis{4-[di(p-anisyl)amino]styryl}-3,

51 g the rate-limiting enzymes in Norway spruce stilbene and flavonoid biosynthesis were actively transc

52 roof of concept we determined gamma of trans-stilbene and found it to be in excellent agreement with

53 nylation from arenes and styrenes to prepare stilbene and stilbene derivatives.

54 were tentatively characterised and included stilbenes and ellagitannins as major components, followe

55 cs revealed that E. polonica transforms both stilbenes and flavonoids to muconoid-type ring-cleavage

56 ermine phenolic acids, flavanols, flavonols, stilbenes and other PCs in the matrices under study.

57 presence of anthocyanins, condensed tannins, stilbenes and phenolic acids, well known for their biolo

58 The LODs and LOQs using FLD for flavanols, stilbenes and phenyl ethanol analogues were improved bet

59 the Scots pine heartwood extractives (mainly stilbenes and resin acids) are synthesized in the cells

60 henolic acids, flavan-3-ols, flavonols and a stilbene) and anthocyanins.

61 exhibited a distinguished profile (lignans, stilbenes) and antioxidant capacity, especially in bound

62 dynamics experiments on trans-stilbene, cis-stilbene, and azobenzene, with excitation to high-lying

63 ]tolane, E-4,4'-bis[di(4-methoxyphenyl)amino]stilbene, and E,E-1,4-bis{4-[di(4-methoxyphenyl)amino]st

64 is no emission similar to that of free trans-stilbene, and the state decays nonradiatively to the gro

65 ids and apocarotenoids, including retinoids, stilbenes, and related compounds.

66 onols, 7 hydroxycinnamic acid derivatives, 2 stilbenes, and several flavan-3-ols.

67 -MS, including phenolic acids, anthocyanins, stilbenes, and the two main isoflavones of soybean, daid

68 The new trans-stilbene annulated uracil derivative "(ts)T" exhibits br

69 he (Z)- or (E)-isomers of azobenzene (AB) or stilbene are used.

70 Stilbenes are a family of bioactive compounds found in p

71 Stilbenes are a small family of phenylpropanoids produce

72 Stilbenes are also derived from lignin during kraft pulp

73 Stilbenes are diphenyl ethene compounds produced natural

74 Plant stilbenes are phytoalexins that accumulate in a small nu

75 However, only a few stilbenes are present in the human diet.

76 Flavonoids and stilbenes are secondary metabolites produced in plants t

77 at, of the Scots pine heartwood extractives, stilbenes are synthesized in situ in the transition zone

78 d should be applicable to many other natural stilbenes as well.

79 the fruit exhibits flavonoid derivatives and stilbenes, as trans-piceatannol and resveratrol, as main

80 improving the biosynthesis of resveratrol, a stilbene associated a range of health-promoting activiti

81 TSs), which catalyze the biosynthesis of the stilbene backbone, seem to have evolved from chalcone sy

82 Compared to the EJ-309 detector, the stilbene-based detector exhibits a lower identification

83 e the development of a family of fluorogenic stilbene-based vinyl amides and vinyl sulfonamides that

84 eted MR contrast agent, Gd-DODAS, based on a stilbene binding moiety and demonstrate its ability to s

85 form of cross talk between the activation of stilbene biosynthesis and the accumulation of anthocyani

86 d MYB15 in the transcriptional regulation of stilbene biosynthesis in grapevine.

87 s, the transcriptional regulation underlying stilbene biosynthesis is unknown.

88 During C. polonica infection, stilbene biosynthesis was up-regulated, as evidenced by

89 ors (TFs) from grapevine, which regulate the stilbene biosynthetic pathway.

90 of the controlled encapsulation state of the stilbene by correlation of fluorescence and (1)H NMR dat

91 on on the reactivity of anodically generated stilbene cation radicals.

92 nfection model and provide new insights into stilbene cellular detoxification.

93 a synthetic route to derivatives of styrene, stilbene, chalcone, cinnamic acid, various fused carbo-

94 Novel stilbene-chalcone (S-C) hybrids were synthesized via a s

95 t peptide amphiphile containing its branched stilbene chromophore covalently linked to the hydrophili

96 and structural dynamics experiments on trans-stilbene, cis-stilbene, and azobenzene, with excitation

97 Therefore, almonds contain the stilbene class of polyphenols in addition to the previou

98 Stilbene cleavage oxygenases (SCOs) cleave the central d

99 echanistic understanding of LsdA and related stilbene-cleaving dioxygenases.

100 Cis-stilbene combretastatin A-4 (CA-4) and a large group of

101 Piceatannol, a promising health-promoting stilbene component, was the major PC in the fruit with a

102 Recently a new derivative of stilbene compound, isorhapontigenin (ISO), was isolated

103 onents being 3,5-dihydroxy-4-isopropyl-trans-stilbene (compound 1) and its stilbene epoxide (compound

104 ilution checkerboard assays to evaluate nine stilbene compounds for their ability to interact synergi

105 rs fast irreversible protonation under these stilbene concentration conditions.

106 t was used to obtain significantly increased stilbene concentration in grapes.

107 To evaluate stilbene concentration, an HPLC-DAD method was validated

108 Tempranillo increased up 200% the total stilbene concentration, Grenache 60% and Graciano 50%.

109 However, stilbene concentrations actually declined during infecti

110 of recent experimental results on control of stilbene conformation and fluorescence in capsules.

111 and the level of sulphur dioxide applied on stilbene content and antioxidant activity have been stud

112 The stilbene content of the must significantly increased wit

113 ffect of pulsed electric fields (PEF) on the stilbene content of three grape varieties.

114 on of the yeast elicitor also enhanced grape stilbene content.

115 seaweed applications to grapevines improved stilbenes content in grapes independently of the season

116 tion capability using organic scintillators (stilbene crystals and EJ-309 liquid scintillators), whic

117 hmark materials such as solution-grown trans-stilbene crystals.

118 The stilbene derivative (Z)-2-(2-bromophenyl)-3-{[4-(1-methy

119 Our studies with a stilbene derivative called TMS (2,3',4,5'-tetramethoxyst

120 we have systematically evaluated a series of stilbene derivatives as myelin imaging agents.

121 a2-Co(NO2)P2W17O61}(8-) as oxidant and trans-stilbene derivatives as substrates point toward a reacti

122 These studies suggested that these stilbene derivatives can be used as myelin-imaging probe

123 igand-based binding assays showed that these stilbene derivatives exhibited relatively high myelin-bi

124 S showed a variety of phenolic compounds and stilbene derivatives in different parts of germinated pe

125 e rigid and structurally simple heterocyclic stilbene derivatives, (E)-3H,3'H-[1,1'-biisobenzofuranyl

126 The XFs, stilbene derivatives, are different from other reported,

127 HU-DNA interface that can be targeted using stilbene derivatives.

128 arenes and styrenes to prepare stilbene and stilbene derivatives.

129 insect infection model, we also observed two stilbene-derived metabolites that were dependent on the

130 The diversification of access to cis-stilbene diamine-derived imidazolines provided by this p

131 ctive aza-Henry approach to nonsymmetric cis-stilbene diamines and cis-imidazolines.

132 otonation of the electrochemically generated stilbene dianion demonstrate that, notwithstanding signi

133 ature voltammetric detection of highly basic stilbene dianions electrochemically generated by the red

134 ification of a porous MOF, Zn(4)O(trans-4,4'-stilbene dicarboxylate)(3), with Br(2) results in diaste

135 Reaction of trans-4,4'-stilbene dicarboxylic acid and zinc nitrate in N,N-dimet

136 kers, 4'-diisothiocyano-2,2'-disulfonic acid stilbene (DIDS) or niflumic acid (NFA).

137 haracterized as a 5,5'-diisothiocyanato-2-2'-stilbene (DIDS)-sensitive transporter in several tissues

138 ribenzoic acid, and 4,4'-diisothiocyano-2,2'-stilbene-disulfonic acid) but decreased under hypertonic

139 lacking TMs 6 and 7 are capable of forming a stilbene disulphonate-sensitive (36)Cl-influx pathway, r

140 of 3dSB-PNBS and dimethoxyphenyl-p-nitro-bis-stilbene (DMP-PNBS), a control compound, we show that th

141 ce for the charge recombination rate between stilbene donor (Sd(+)) and stilbene acceptor (Sa(-)) lin

142 the purine or pyrimidine blocks of a diblock stilbene donor-acceptor capped hairpin with locked nucle

143 s are easily distinguished from those of the stilbene donor/acceptor radical ion chromophores.

144 Tapinarof is a stilbene drug that is used to treat psoriasis and atopic

145 nsport dynamics of DNA hairpins possessing a stilbene electron acceptor and donor along with a modifi

146 occupation during charge transport between a stilbene electron donor and acceptor.

147 complexes of DNA capped hairpins possessing stilbene electron-acceptor and -donor chromophores separ

148 ation, the contents in piceatannol and other stilbenes, ellagitannins, and flavonols decreased while

149 rovide a structural view for stereoselective stilbene epoxidation and functionalization in an inverte

150 However, stilbene epoxidation biosynthesis and its biological rol

151 urements and the isomeric distributions of Z-stilbene epoxidation products demonstrate that the activ

152 from Photorhabdus luminescens that catalyzes stilbene epoxidation.

153 sopropyl-trans-stilbene (compound 1) and its stilbene epoxide (compound 2).

154 (in THF) identical to the spectrum of trans-stilbene, except for [o-MeStilSiO(1.5)](8), which exhibi

155 V-vis absorptions are not changed from trans-stilbene, except for the ortho derivative, which is blue

156 While in trans-stilbene, excitation at 6 eV induces a phenyl twisting m

157 s paper reports the use of a grapevine-shoot stilbene extract (Vineatrol(R)) as a preservative in red

158 d energy was the most effective on the total stilbene extraction.

159 beta-CD was the most effective in recovering stilbenes, flavonols, and flavan-3-ols from grape pomace

160 High-resolution images of the stilbene fluorescence provided by macroscopy were supple

161 show that the prolonged luminescence is not stilbene fluorescence.

162 order of 100 pN were generated using a stiff stilbene force probe.

163 ses (SCOs) cleave the central double bond of stilbenes, forming two phenolic aldehydes.

164 was identified as isorhapontigenin (ISOR), a stilbene found in traditional Asian medicinal plants.

165 Therefore, we characterised stilbenes from Nonpareil, Butte and Carmel almond (Prunu

166 ever, is markedly decreased as the number of stilbene functional groups is increased.

167 precursor, such as Pd((R,R)-Me-Duphos)(trans-stilbene), gave the tertiary phosphines PMe(Ar')(Ar) in

168 P2-19G2 that has been elicited against trans-stilbene has unprecedented ability to produce bright lum

169 eratrol, the basic unit of all other complex stilbenes, has received widespread attention because of

170 rge separation in capped hairpins in which a stilbene hole acceptor and hole donor are separated by A

171 and the highest occupied state (pi state on stilbene), however, is markedly decreased as the number

172 Interestingly, the respective individual stilbene (IC(50) > 100 muM), chalcone (IC(50) = 11.5 muM

173 It is found that the geometry of trans-stilbene in the ground as well as in the first excited s

174 r than that of red grapes, a major source of stilbene in the human diet.

175 c uphill conversion of trans-stilbene to cis-stilbene in the presence of blue light-emitting diodes w

176 nd emission spectra of free and encapsulated stilbene in two different capsules were calculated using

177 0) values (vs Fc(0/+)) for substituted trans-stilbenes in acetonitrile and (N111)(N112)BH2-NTf2 do no

178 oved the synthesis of trans-piceid and total stilbenes in both seasons.

179 re suitable for the determination of several stilbenes in complex samples.

180 es in the presence of base to generate trans-stilbenes in good to excellent yields (up to 99%).

181 sion and in the accumulation of glycosylated stilbenes in planta.

182 ation, whereas a more localized synthesis of stilbenes in stomata guard cells and cell walls is induc

183 The anion radicals of stilbenes in the collisionless isolated phase were synth

184 f thermal isomerization of constrained stiff stilbene increase sharply as the restoring force decreas

185 The stilbene inhibitors induce gene expression changes in Mt

186 conversion of tapinarof and related dietary stilbenes into novel dimers.

187 ollowed to isolate and identify this unknown stilbene is described in the present work.

188 cage, the ground state of encapsulated trans-stilbene is distorted, with the two phenyl groups twiste

189 ective reductive coupling of benzaldehyde to stilbene is driven by subsurface Ti interstitials on vac

190 A rather uniform synthesis of stilbenes is induced after UV-C irradiation, whereas a m

191 hotocyclization reaction of dissymmetric bis-stilbenes is reported.

192 Resveratrol (3,5,4'-trihydroxy-trans -stilbene) is a well-known polyphenolic compound of red w

193 Piceatannol, a natural stilbene, is an analog and a metabolite of resveratrol.

194 these polyphenolic compounds - polyketides, stilbenes, isoflavones and catechins.

195 The ranking of catalysts by (Z)-stilbene isomerization initial rates is Ni-Ga >> Ni-Sc >

196 talytic reactions: DPA hydrogenation and (Z)-stilbene isomerization.

197 eV induces a phenyl twisting motion, in cis-stilbene it leads to an ultrafast ring-closing to form 4

198 studies established their structures as new stilbene-l-proline conjugates, prolbenes A (compound 3)

199 ondingly, NOV1 cleaves a wide range of other stilbene-like compounds with a 4'-OH group, offering pot

200 In both cases, the rigidity of the stilbene linker increases upon coordination to the inorg

201 d spectroscopic measurements reveal that the stilbene linkers in the dense structure 1 exhibit a smal

202 coordination environments connected by trans-stilbene links.

203 When tested on several substituted stilbenes, LsdA exhibited the greatest specificity for l

204 tramolecular [2+2] photocyclization of a bis-stilbene macrocycle was studied.

205 dulation of genes related to phenylpropanoid/stilbene metabolism highlighted the distinct metabolomic

206 gies mirror the relative polarization of the stilbene moieties and can be quantitatively correlated w

207 ne core was identified as replacement of the stilbene moiety.

208 freezing-in of orientational disorder of the stilbene molecule.

209 eries of highly luminescent oxadiazole-based stilbene molecules (OXD4, OXD8, OXD10, and OXD12) exhibi

210 erization reaction to take place between two stilbene molecules in the solid state.

211 ctive metabolite of the family of prenylated stilbenes named schweinfurthins, is only located in thes

212 ation of four simple phenylpropanoids, eight stilbenes, nine flavonoids, six related arithmetic param

213 Neither stilbene nor naphthalene are reduced by 1, but 1 reduces

214 The epoxidation of cis-stilbene occurred in the cavity of 14(out)-Mn(III)-1 and

215 ce imaging was developed to localize in situ stilbenes on the same stressed grapevine leaves.

216 on of 1a afforded predominantly either trans-stilbene or diphenyl glyoxime depending on solvent, temp

217 The SiPMs are coupled to the ends of eight stilbene organic scintillators, which have an overall vo

218 ts of selectivity, for two substrates: trans-stilbene oxide (t-SO) and trans-diphenylpropene oxide (t

219 trans-Stilbene oxide (TSO) induces drug metabolizing enzymes i

220 larly to the assay that used radioactive cis-stilbene oxide but with a greater discrimination between

221 The rearrangement of cis-stilbene oxide catalyzed by Al(2)O(3) was studied in the

222 a family of 1,2-diamines derived from trans-stilbene oxide that prevent HCV infection at nontoxic, l

223 activity against both epibromohydrin and cis-stilbene oxide, but with a relatively narrow range of su

224 Phenolic acids, flavanols, flavonols and stilbenes (PAFFS) were isolated from whole grapes, juice

225 enzothieno[3,2-b][1]benzothiophenes, via the stilbene pathway, is described.

226 periment and show that fluorescence of trans-stilbene persists in the large cage while it is quenched

227 an anthracene to generate the triptycene, a stilbene photocyclization to construct the helicene, and

228 dies revealed that CDs were able to increase stilbene photostability at 4 degrees C.

229 Stilbene phytoalexins, namely resveratrol, pterostilbene

230 nteraction of the silicon center(s) with the stilbene pi* orbital in both the corner and half cages.

231 proposed to result from interactions of the stilbene pi* orbitals with a LUMO centered within the ca

232 complex supported by an original switchable stilbene platform.

233 Stilbene polyphenols are present in some fruits and nuts

234 thases (CHSs) several times independently in stilbene-producing plants.

235 A series of symmetrical E-stilbene prolinamides that originated from the library-s

236 However, the content of stilbene represented by trans resveratrol-3-glucoside wa

237 for the first time provide evidence that the stilbene resveratrol targets PTP1B to inhibit PDGFR mito

238 -glucoside and quercetin 3-glucoside and the stilbenes resveratrol, piceatannol, astringin and isorha

239 ging, the goal of this study was to increase stilbenes (resveratrol (RV), pterostilbene (PT) and pino

240 rape and wine are the main dietary source of stilbenes, resveratrol and piceid being the most common

241 The total synthesis of the natural stilbene (+)-schweinfurthin G (8) has been accomplished

242 c DNA hairpins possessing donor and acceptor stilbenes separated by one to seven A:T base pairs.

243 ntinuation of our exploration to improve the stilbene series, the 3,5,6,8-tetrasubstituted quinoline

244 Direct irradiation of trans-stilbene showed that C(5)G3 and C(4)G3 dendrimers afford

245 onomer, is essential for transduction of the stilbene signal into p53-dependent apoptosis of breast c

246 shifted by approximately 20 nm, as found for stilbene-siloxane macrocycles, suggesting some interacti

247 emission spectra characteristic of monomeric stilbenes, similar to the dicarboxylic acid in dilute so

248 , we show how a molecular force probe, stiff stilbene, simplifies force spectroscopy of localized rea

249 Stilbene solubility was improved by the formation of inc

250 This work showed that stable stilbene solutions can be achieved using hydroxypropyl-C

251 to consistent and complementary data on the stilbene spatial distribution for the two stresses addre

252 A set of stilbene-substituted octasilicates [p-RStil(x)Ph(8-x)SiO

253 antimicrobial activities compared with their stilbene substrates, suggesting a metabolite attenuation

254 rticipation in defense mechanisms in plants, stilbenes, such as resveratrol, display important pharma

255 The stereospecific formation of trans-stilbene suggests a mechanism of decomposition in which

256 ion of phenylalanine ammonia-lyase (PAL) and stilbene synthase (STS) genes, followed by a rapid accum

257 A ligase (At4CL1) and Vitis vinifera (grape) stilbene synthase (VvSTS) to increase resveratrol levels

258 s evidenced by elevated transcript levels of stilbene synthase genes.

259 ENESIS-RELATED1, PATHOGENESIS-RELATED10, and stilbene synthase in PM-infected V. vinifera, suggesting

260 Although stilbene synthases (STSs), the key enzymes responsible f

261 Stilbene synthases (STSs), which catalyze the biosynthes

262 Among them, we identified genes of stilbene synthases, PR-10 proteins, and several transcri

263 t a conceptually different approach toward E-stilbene syntheses by photoinduced direct C-H arylation

264 emically generated by the reduction of trans-stilbene (t-Stb) and its derivatives (4-methoxy-, 2-meth

265 is achieved when the concentration of trans-stilbene, [t-Stb], appreciably exceeds the concentration

266 alog of resveratrol (3,5,4'-trihydroxy-trans-stilbene), termed DHS (trans-4,4'-dihydroxystilbene), th

267 Pawhuskin A is a prenylated stilbene that functions as an antagonist of the kappa op

268 (NO2)P2W17O61}(8-) and one molecule of trans-stilbene that is sufficiently stable at room temperature

269 erein, we report on boronic acid-substituted stilbenes that limit TTR amyloidosis in vitro.

270 ssion strongly increased the accumulation of stilbenes that play a role in plant defense and human he

271 s was screened to identify substituted trans-stilbenes that were more active than resveratrol.

272 The substituted trans-stilbenes that were potent inhibitors of the activation

273 ecipitons (1,2-biphenylethenes; analogous to stilbenes) that are activated by a covalently attached o

274 he photocatalytic uphill conversion of trans-stilbene to cis-stilbene in the presence of blue light-e

275 he in-solution oxidative photocyclization of stilbenes to phenanthrenes is a well-known and synthetic

276 C. polonica converted stilbenes to ring-opened, deglycosylated, and dimeric pr

277 The content of the stilbenes trans-resveratrol and piceid as well as the an

278 d and calculated for planar ring-fluorinated stilbenes, trans-2,3,5,6,2',3',5',6'-octofluorostilbene

279 ereo- and regioselectivity in solution-state stilbene-type photocycloadditions.

280 has 3-D symmetry, it appears that all of the stilbene units interact in the excited state, consistent

281 lts in diastereoselective bromination of the stilbene units.

282 preparation of nonsymmetrically substituted stilbenes using a one-pot two-step double Heck strategy.

283 added) and experimental (reduction of trans-stilbene) voltammograms to assess the capabilities of pa

284 A new, previously undescribed-in-grapes stilbene was found after UVC treatment.

285 At 25 degrees C in chloroform, while trans-stilbene was still the major product, some diphenyl glyo

286 Stilbenes were isolated from ethanolic almond extracts b

287 f flavonols, anthocyanins, flavan-3-ols, and stilbenes, were detected.

288 e phenanthrene formation, in addition to cis-stilbene, whereas C(3)G3 and C(2)G3 gave only cis-stilbe

289 Resveratrol is a stilbene, which is one of a group of polyphenols in many

290 on a flexible and emissive linker molecule, stilbene, which retains its luminescence within these so

291 ates are always the pi and pi* states on the stilbene, which show very weak shifts with increasing de

292 ncentration of phenolic compounds, including stilbenes, whilst treatments with kresoxim-methyl, fluqu

293 Benzaldehyde reductively couples to stilbene with 100% selectivity and conversions of up to

294 l symmetry, indenoindene, a carbon-bridged E-stilbene with a centrosymmetry, shows elongated pi-conju

295 nteraction between oxyresveratrol (a type of stilbene with high biological activity) and modified cyc

296 t discovery of high amount of piceatannol, a stilbene with potent biological activities, highlight th

297 An interest in the schweinfurthins, natural stilbenes with significant antiproliferative activity, h

298 Photorhabdus species produce a family of stilbenes, with two major components being 3,5-dihydroxy

299 nd confirmed the expected orientation of the stilbene within the TTR binding sites.

300 esveratrol and a series of substituted trans-stilbenes without hydroxy groups were compared with resv