ライフサイエンスコーパス: isomer

1 o a stretching force of 1-2 nN (depending on isomer).

2 isomer after the addition of only 10% of the isomer.

3 olarization and molecular properties of each isomer.

4 eoyl glucose was found to be the predominant isomer.

5 Z-isomer of which is less potent than the E-isomer.

6 third step leads back to the stretched trans isomer.

7 angement to the energetically favorable para isomer.

8 (3) which in solution is converted to the E-isomer.

9 ces of detecting and even isolating the bird isomer.

10 l quantities of a kinetically favored olefin isomer.

11 were explored and shown to be conformational isomers.

12 the relative stability of the peroxy radical isomers.

13 reversibly transforms to pre-vitamin D3 type isomers.

14 sections, enabling powerful analysis of many isomers.

15 stable than the corresponding pi-conjugated isomers.

16 ation of the cis faster than their all-trans isomers.

17 he nature of the features distinguishing the isomers.

18 est affording small amounts of the tail-tail isomers.

19 9% yield with a general preference for the E-isomers.

20 fractional tuning of the two configurational isomers.

21 g the stereochemically challenging anti-anti isomers.

22 tic interconversion zone between the E and Z isomers.

23 iding a second method for distinguishing the isomers.

24 dence for the relative population of the two isomers.

25 o search for these interesting and important isomers.

26 eltaDeltaDelta and LambdaLambdaLambdaLambda) isomers.

27 OH group forming six distinct peroxy radical isomers.

28 hat it contained TBPP isomers instead of ITP isomers.

29 h n > 3, as well as other metastable C6H6(+) isomers.

30 rmined the activity of the individual olefin isomers.

31 eas iso 18:0 was discriminated from cis-16:1 isomers.

32 tion) to give a mixture of in,in and out,out isomers.

33 tein binding from a mixture of equilibrating isomers.

34 OS) and their respective linear and branched isomers.

35 (mean +/- SD: 0.13% +/- 0.04%) and trans ALA isomers (0.05% +/- 0.01%) in 395 erythrocyte samples col

36 f both X1B and X2B were a monogalloylglucose isomer (1), a HHDP-glucose isomer (2), castalin (3) gall

37 highly stable conformation of the so-called isomer 2(B) has been obtained for full-length guanylin,

38 Equilibration of 1 with its 2,3-dihydro isomer 2, which is chiral and racemic, by base-catalyzed

39 onogalloylglucose isomer (1), a HHDP-glucose isomer (2), castalin (3) gallic acid (4), vescalagin (5)

40 erization of methylenedianiline (MDA) 2-ring isomers (2,2'-, 2,4'-, and 4,4'-MDA) is reported using m

41 series of bidentate bis(pyridine) anthracene isomers (2,3-PyAn, 3,3-PyAn, 2,2-PyAn) that differ in th

42 he E-isomers (4-6) or predominantly as the Z-isomer (3) which in solution is converted to the E-isome

43 yptophan, chrysoeriol-6,8-di-C-pentoside and isomers 4, 5, 9 and 12 of diferulic acids key compounds

44 le bond was synthesized in the form of the E-isomers (4-6) or predominantly as the Z-isomer (3) which

45 The effect of the chlorogenic acid isomer 5-O-caffeoylquinic acid (5-CQA) on digestion of p

46 d all-trans-astaxanthin, two cis-astaxanthin isomers, 5 astaxanthin monoesters, and 10 astaxanthin di

47 The two isomers 6 and 9 of cis(4,4'-)-dicarbomethoxydibenzo-27-c

48 nyls (PCBs), 3 hexabromocyclododecane (HBCD) isomers, 6 mycotoxins, 6 inorganic compounds) together w

49 the trans isomer has a stretched and the cis isomer a compact form.

50 These two isomers accounted between 4.2 and 86% of the mutagenicit

51 DFT calculations indicate that the [1,2-a]-isomer adopts a twisted, helical C2-symmetric structure

52 ds in both switching directions, i.e. >90% E isomer after irradiation with 470 to 530 nm light and 99

53 ned at the mobility of OTFTs having pure syn isomer after the addition of only 10% of the isomer.

54 The cis-isomers align in the main 12-membered ring (MR) channel

55 treated with varying concentrations of each isomer alone and in different combinations revealed that

56 ortho-tetrachlorobenzoquinone over its para-isomer and 1,3-cyclohexadiene over its 1,4-isomer, perha

57 s with the addition of only 0.01% of the syn isomer and is pinned at the mobility of OTFTs having pur

58 (IMS) has proven to be useful in separating isomer and isobar ions; however, IMS-MS suffers from dec

59 to matrix effects, difficulty in separating isomer and isobaric ions, and long analysis times.

60 Following this route produces a pure cis-isomer and more surprisingly, predicts that graphane is

61 ioning of the dark state between the product isomer and the original ground state.

62 ent of the stoichiometry of the two PSI-LHCI isomers and changes in the oligomeric state of the PSI-L

63 ng with their (omega)-linked or alpha-methyl isomers and ethanolamide derivatives, as well as 2-hydro

64 tial energy surface (PES) between (C2H2)n(+) isomers and provide evaporative cooling to dissipate the

65 ddition of TrFE: the cis and trans head-tail isomers and the trans head-head isomer, where the CHF gr

66 tral separation of the individual azobenzene isomers and their quantum yields.

67 1 to 10:1 for 20 examples), favoring the cis-isomer, and good to excellent enantioselectivity (70-91%

68 hosphorus FRs (PFRs), 2 Dechlorane-Plus (DP) isomers, and 3 hexabromocyclododecane (HBCDD) isomers in

69 somers that were baseline resolved, four dp6 isomers, and the observation of a dp3 oligosaccharide.

70 The respective ratios of L2Ni(C4F6H2) isomers are influenced by the nature of L, with smaller

71 spontaneous cis-trans isomerism, and the cis isomers are much more difficult to stabilize than the tr

72 the complex, corresponding to two different isomers, are populated at room temperature, and the two

73 lpha-conotoxins have focused on the globular isomers as the ribbon and bead isomers typically have lo

74 rization between the two product merocyanine isomers, as well as their ring-closure reaction back to

75 asurements currently possible for individual isomers at very low temperature and observations of isom

76 the experimental data available for selected isomers at very low temperature, the present results pro

77 The data shows that the lactose isomers beta-d-Galp-(1-->2)-d-Glcp, beta-d-Galp-(1-->3)-

78 organic product obtained from the head-tail isomers: BF3.OEt2 is selective for 1,1,2,3-tetrafluorocy

79 These results suggested that the two isomers bind simultaneously to the enzyme but within dif

80 , HPW) are more stable than less substituted isomers but are destabilized within smaller concave envi

81 be used to discern cis and trans double-bond isomers by virtue of the differences in the fragmentatio

82 The two cage isomers can coexist in solution and interconvert.

83 rred (from DFT calculations) trans head-head isomer (cf. 50% with PMe3) and the largest affording sma

84 solving power needed to separate the various isomer classes.

85 ion of distinct product ion spectra for each isomer, clearly indicating the binding sites for the maj

86 for the Eigen H3O(+)(H2O)3 and D3O(+)(D2O)3 isomers compare very well with experiment.

87 e ternary complex generates the active trans-isomer competent for carbonyl bond activation by active-

88 When DMS could not separate cis and trans isomers completely, as was the case with sphingomyelins,

89 In this regime, beta hydroxy peroxy radical isomers comprise approximately 95% of the radical pool,

90 obility of OTFTs to drop with increasing syn-isomer concentration.

91 n half-lives adopt a T-shaped ground state Z isomer conformation and proceed through a T-shaped isome

92 that have a twisted (rather than T-shaped) Z isomer conformation.

93 For the first time, the cis/trans isomer content of menaquinone-7 in food products has bee

94 , the presence of one hexachlorinated OH-CTT isomer could be verified in the samples, which was about

95 ryl moieties, the thermal stability of the Z-isomers could be enhanced while maintaining the advantag

96 ng the hydrazonation reaction, as only the E-isomers could undergo chelation-controlled reduction.

97 Under aerobic conditions, 4-MCHM isomers degraded to nondetectable levels within 4 days.

98 whereas transformations of the nitroso oxide isomers derived from 1b led to a set of stable products:

99 l suited to identify and characterize glycan isomers directly, which presents tremendous challenges f

100 ion remains unanswered: why has only the 2,4-isomer emerged as a labile protecting group?

101 injection of EP-3533, or of its non-binding isomer EP-3612.

102 For the majority of isomers evaluated in this study, a uniform field-based r

103 e populated at room temperature, and the two isomers exchange on a timescale of a few picoseconds.

104 Under these conditions, geometric isomers exhibited different IMS arrival time distributio

105 ery distinct bands corresponding to isolated isomers experiencing or not the nN --> sigma*N-H electro

106 ct isomers, presumably TTC and TTT cis-trans isomers, for the open-ring merocyanine product, and disc

107 In ESI, 2-ring MDA isomers formed single unique [M + H](+) (199 Da) parent

108 As the syn isomer fraction increases, intermolecular repulsion incr

109 sed photoisomerisation showed that the (5'Z)-isomer gazaniaxanthin is the main (Z)-isomer of rubixant

110 Each isomer had unique electronic responses in the presence o

111 roperties (quantitative switching and long Z isomer half-life).

112 We identify compounds with Z isomer half-lives ranging from seconds to hours, to days

113 s consists of two states, in which the trans isomer has a stretched and the cis isomer a compact form

114 One isomer has been fully characterized in the Ir(V) state,

115 arison with three other known BN naphthalene isomers has established two guiding principles for predi

116 In addition, the Z-isomers have long thermal half-lives in the dark of up t

117 ysis shows that while CS and HS disaccharide isomers have similar drift times, they can be uniquely d

118 of BN acene compounds: (1) Orientational BN isomers have similar HOMO-LUMO gaps.

119 ond are converted by UV irradiation to the Z-isomers having bifurcated O-H...O...H-X hydrogen bond.

120 The E-isomers having intramolecular O-H...O horizontal lineC h

121 ) cluster have shown that the global minimum isomer I possesses a geometric structure which resembles

122 ficulties to be resolved from its structural isomer (i.e., phosphatidylglycerol, PG, another low-abun

123 d to reduce the energy disorder by isolating isomer ICBA-tran3 from the as-synthesized ICBA-mixture.

124 ver, the lack of formation of the anthracene isomer implies that HACA alone cannot be responsible for

125 delta-Tocotrienol was the most stable isomer in both forms during storage and when incorporate

126 isotropy analysis, for which the trans (cis) isomer in DOPC (DPPC) presents a fast decay time.

127 C bond formation transition state to the S-E isomer in the case of MeQd and the R-E isomer with TMSQ

128 lative contribution of the trans double-bond isomer in the mixed samples.

129 tate derived from the participation of the E isomer in the reaction.

130 expense of 15-anti, which is the predominant isomer in the wild type, and abolishes the peak current

131 phate (B2IPPPP) being the most prevalent ITP isomers in both mixtures.

132 The content of cis/trans isomers in certain dietary supplements exceeded the cont

133 the contribution of individual ITP and TBPP isomers in four commercial flame retardant mixtures: FM

134 rugs as Celebrex and SC-560 as well as their isomers in gram scale.

135 h is known but less common than other Keggin isomers in polyoxometalate and polyoxocation chemistry.

136 Relative concentrations of the isomers in solutions have been determined with the stand

137 somers, and 3 hexabromocyclododecane (HBCDD) isomers in the 95 dust samples.

138 antioselective hydrogenation for both olefin isomers in the case of alpha,beta-dialkylvinyl esters.

139 ) data, could be correlated to denticulatain isomers in the extracts.

140 tic interaction was observed between the two isomers in the GGDPS enzyme assay.

141 n spectrum discovered the coexistence of two isomers in the ion beam, including the one with the Al=A

142 ionisation efficiency of vitamin D3 and its isomers in UHPLC-MS/MS and improved the separation and f

143 nd 3, we revealed two calix[2]pseudorotaxane isomers in which the calix-wheel adopts 1,2,3-alternate

144 opoisomers (i.e. "frozen-out" conformational isomers) in solution leads to complex mixtures.

145 acterization of the separated constitutional isomers indicated that they possess different melting po

146 ffered from FM 550 in that it contained TBPP isomers instead of ITP isomers.

147 Both cis and trans isomers interact with transcriptional regulators, sugges

148 The syntheses of these two isomers involved symmetrical disubstituted alkynes that

149 Polymerization to cis-isomer is kinetically preferred at low temperature, not

150 Formation of the product isomer is observed in real time by FSRS.

151 omer is the most reactive, whereas the ortho isomer is oxidized fastest in nonpolar solvents.

152 C-C bond formation by the cis-isomer is suppressed by hydrogen bonding of the cis-alde

153 main (Z)-isomer of rubixanthin and the (13Z)-isomer is the main (Z)-isomer of lycopene.

154 solvent: in highly polar solvents, the meta isomer is the most reactive, whereas the ortho isomer is

155 ycolytic interconversion of phosphoglycerate isomers is catalysed in numerous pathogenic microorganis

156 Another isomer, isotachysterol, was formed under acidic conditio

157 lly promote the polymerization of one of the isomers (l or d) with respect to the other.

158 Lutein and Zeaxanthin isomers (L/Zi) may counteract reactive oxygen species pr

159 creased by the co-analysis of its structural isomer, lactosylceramide (LacCer), which is not an alpha

160 show that locking the switch into the trans isomer leads to shortened circadian periods.

161 llylamines, whereas the transformation (S,E)-isomers leads to (R)-allylamines.

162 Carboxyl group of syn-isomers may also participate in the inactivation of free

163 is preferred at the GGDP site, and that both isomers may bind to the enzyme simultaneously.

164 nonprotease-cleavable enantiomer, the VC(R) isomer, mediated effective cell killing with a cysteine-

165 l isomers of this cluster and the role these isomers might play in the IR spectra.

166 at very low temperature and observations of isomer mixtures at ambient conditions.

167 e and p-tolualdehyde leads to the open-chain isomers, namely (2-hydroxybenzylidene)hydrazono-2-phenyl

168 es, and heteroanalogues) and the other known isomers, namely, corrphycene, hemiporphycene, and isopor

169 ternary S,N,O anions such as the structural isomers NSO(-)/SNO(-) and SSNO(-) are rarely mentioned i

170 al characterization of a monohydrido bridged isomer of a ditetrelene.

171 to be general, implying that the metastable isomer of a photoswitch can be isomerized to the more st

172 is of either the E or Z alkene from a single isomer of a vinyl coupling partner.

173 act to enhance the concentration of the cis isomer of glyoxal at the water interface.

174 xanthin and the (13Z)-isomer is the main (Z)-isomer of lycopene.

175 However, the first constitutional isomer of porphyrin, porphycene, was not synthesized unt

176 ducing sizable concentrations of acetone, an isomer of propionaldehyde.

177 (5'Z)-isomer gazaniaxanthin is the main (Z)-isomer of rubixanthin and the (13Z)-isomer is the main (

178 This natural isomer of spiroscytalin showed moderate activity against

179 A single conformational isomer of the (L)P diastereomer, [YA(L)PAA+H](+), is fou

180 ngly, the spontaneous resolution of chiral S-isomer of the 1-SH adduct occurred during crystallizatio

181 shift affords stereospecifically the E or Z isomer of the 5-alkenyl-4-iminohydantoin products from t

182 ochemistry of its alkene; alternatively, one isomer of the compound can be subjected to stereoselecti

183 The cis-isomer of the d-G3P aldehyde, representing the dominant

184 llows precise quantification of each E and Z isomer of the enantiomer.

185 The trans isomer of the keto-acid products is also observed at var

186 group at the C3-position favors the C-bound isomer of the ligand-supported palladium(II) complexes a

187 The least stable isomer of the parental BN naphthalene series has been sy

188 The new anion is a positional isomer of the recently reported "staggered" stannyl-liga

189 revealed the conversion of the cis to trans isomer of unsaturated fatty acid upon short-term nZVI ex

190 an 18-membered-ring enzyme inhibitor), the Z-isomer of which is less potent than the E-isomer.

191 inazolin-4(3H)-one nucleus of both aS and aR isomers of 1 had a critical effect on the inhibitory act

192 The Ar((i)Pr4) isomers of 2a and 3a, i.e., [Ar((i)Pr4)Sn(C2H5)]2 (2b) a

193 (SPME) method to quantify the cis- and trans-isomers of 4-MCHM.

194 The ortho, meta, and para isomers of 9,10-dipyridylanthracene 1 have been synthesi

195 We have prepared and fully characterized two isomers of [Ir(IV) (dpyp)2 ] (dpyp=meso-2,4-di(2-pyridin

196 Included in the study are all 20 isomers of C6HnF(5-n)B(OH)2 with half-lives spanning 9 o

197 Five different isomers of cis/trans vitamin K2MK-7 were identified.

198 After verifying that the aS and aR isomers of compound 1 do not interconvert in solution, w

199 Serum concentrations of p,p' isomers of DDT and DDE were above the limit of detection

200 Out of six possible positional isomers of dinitrophenol, only 2,4-DNP has been used ext

201 The [2,1-a]- and [1,2-a]-isomers of fluorenofluorenedione have been synthesized v

202 This suggests the two isomers of fluorohistidine can also serve as probes of t

203 ecent report showed that the bead and ribbon isomers of GeXIVA are more potent than the globular isom

204 roscopy for the identification of positional isomers of hydroxy-atorvastatins, the primary metabolite

205 These mixtures contain isomers of isopropylated and tert-butylated triarylphosp

206 ification and quantification of types of (Z)-isomers of lycopene and rubixanthin in both rosehips and

207 nd acyl-CoA as acyl donors and, 1- or 2-acyl isomers of lysophosphoplipids as acyl acceptors.

208 a family of powerful odorants, including the isomers of mintlactone and menthofurolactone that occur

209 ein report the preparation of constitutional isomers of pentahydroxy-functionalized pillar[5]arenes v

210 carrier that binds the all-trans and 11-cis isomers of retinal and retinol, and this facilitates the

211 ene indole alkaloids either through multiple isomers of strictosidinic acid or strictosidine.

212 Cis/trans and anti-isomers of studied cinnamic acid derivatives may scaveng

213 and other seed oils, while the (2)D allowed isomers of TAG containing 18:3 fatty acyl chains as well

214 nt, including para-functionalized structural isomers of the type M2(p-dobdc) (p-dobdc(4-) = 2,5-dioxi

215 s from the existence of higher-energy Zundel isomers of this cluster and the role these isomers might

216 A novel method of marking isomers of vitamin K2MK-7 in dietary supplements was dev

217 uene, ethylbenzene, and the three structural isomers of xylene (BTEX) in the concentration range of 0

218 However, coexisting structurally similar isomers often render an unambiguous identification impos

219 i-substituted borate anion consisting of two isomers, one with both nitramido ligands attached to B t

220 ectively give alpha-fluoro-nitroalkenes as Z-isomers only.

221 Trans-isomer OSDA leads to the small-pore zeolite SSZ-39 with

222 alf ( approximately 60%) of all hypothetical isomer pairs, including leucine and isoleucine, whereas

223 a-isomer and 1,3-cyclohexadiene over its 1,4-isomer, perhaps hinting at the potential for concerted 2

224 different combinations revealed that the two isomers potentiate the induced-inhibition of protein ger

225 thin, gomphrenin I, phyllocacthin, and their isomers predominated.

226 could also generate alpha-terpineol with (R)-isomer preference.

227 natural product in 69 % yield from the minor isomer present in an equilibrating mixture of labile ena

228 For most juices, cis-isomers presented a higher bioaccessibility than their a

229 spectra, we identify two spectrally distinct isomers, presumably TTC and TTT cis-trans isomers, for t

230 tion of the cofactor, for which two distinct isomers, prFMN(ketimine) and prFMN(iminium), have been o

231 nal matrix of isotopic shifts is specific to isomers, providing a fundamentally new approach to the c

232 oxazol-5(3H)-ylidene)ethanal (10), the trans isomers recombined forming the corresponding nitro and n

233 efins capable of precisely targeting a given isomer regardless of the nature of the features distingu

234 Here, we use isomer-resolved measurements of the reaction products of

235 (150 and 25 pg/m(3) (sum of alpha- and beta-isomers), respectively).

236 hium enolate mixed dimers containing E and Z isomers, respectively.

237 d (4), vescalagin (5), and grandinin (or its isomer roburin E, 6).

238 ypically, switching from more to less stable isomer(s) is performed by irradiation with UV or visible

239 ith an half-life of about 10 s, evidenced by isomer-selective two-color (IR-IR) spectroscopy.

240 rity of the highest affinity HMO ligands (or isomer sets that contain the highest affinity ligands) i

241 ctra of 2, 6, 8, and 9 show a clear trend in isomer shift (delta), with a decrease in delta as metal-

242 pectra for the cis and trans-Zundel and ring isomers show prominent features that do not match with e

243 (199 Da) parent ions, whereas in MALDI each isomer shows significant formation of three precursor io

244 g of the photoelectron spectrum of the ortho isomer shows that the ground state of the anion is a tri

245 Isomer-specific removal rates were positively correlated

246 chiral drugs and metabolites, constitutional isomers, stereoisomers, and organohalogenated species.

247 ate sn-positional and double-bond-positional isomers, such as the regioisomeric phosphatidylcholines

248 ried products distribution, depending on the isomer tested.

249 n the separation and identification of lipid isomers that differ only in site(s) of unsaturation or g

250 which should consider not only charge state isomers that include salt bridges but also protonation a

251 dies are the first to report a set of olefin isomers that synergistically inhibit GGDPS, thus establi

252 zation (dp) ranging from dp4 to dp8, two dp4 isomers that were baseline resolved, four dp6 isomers, a

253 ve been able to estimate in the photoinduced isomer the distance between hydrogen atom and carbon ato

254 (2) For each pair of orientational BN isomers, the more thermodynamically stable compound has

255 by the MS/MS spectra, enabling the different isomers to be distinguished.

256 ty switch, allowing both linear and branched isomers to be prepared with high selectivity in an effic

257 ate studies trace the preference for E and Z isomers to tetrasolvated- and pentasolvated-monomer-base

258 s acidic MCl2; cagelike adducts of the in,in isomer, trans- Cl2(P((CH2)14)3 P) (M = 2/Pt, 3/Pd, 4/Ni)

259 f first-principles calculations, we find two isomers, two-atom wide ribbon and single-atom chain, lin

260 the globular isomers as the ribbon and bead isomers typically have lower potency at nAChRs than the

261 addition, the Z-delta hydroxy peroxy radical isomers undergo unimolecular 1,6 H-shift isomerization.

262 ant formation of three (of the possible six) isomers upon oxidative cycloaddition of TrFE: the cis an

263 Conversion was only observed for the cis-isomer, verifying that this is a true intermediate and n

264 c equilibration with the [Zr]-O-CH2-B(C6F5)2 isomer was deduced, which showed typical reactions of an

265 The cis-beta-carotene isomer was significantly increased after processing but

266 ed to a set of stable products: the cis/anti isomer was transformed into (3,4,7-trimethyl-3a,4-dihydr

267 oso compounds, and the most reactive cis/syn isomer was transformed into ortho-nitrosobenzyl alcohol

268 distribution of the different constitutional isomers was dependent on the nature of the substitution,

269 ences in experimental pKa values between the isomers was found to arise from solvation effects, provi

270 Identification of cis/trans isomers was performed by HRMS-QTOF, whereas their quanti

271 lanthracene (DPA) acceptor mediated by these isomers was used as a proxy for the efficacy of orbital

272 ridged (Si(H)SiH) and di-bridged (Si(H2 )Si) isomers, was initially formed in the gas-phase reaction

273 (TBECH or DBE-DBCH) and the pure beta-TBECH isomer were subjected to in vitro biotransformation by h

274 while those for the beta-, gamma-, delta-HCH isomers were -29.0 +/- 0.3 per thousand, -29.5 +/- 0.4 p

275 ) in >/=98% of the samples, whereas the o,p' isomers were above the LOD in at least 80% of the sample

276 on, six molecular probes using available DNP isomers were developed and investigated to evaluate the

277 ic conditions, two cis-trans styrylflavylium isomers were identified, which could be interconverted d

278 bitrap MS system, isobaric peptide and sugar isomers were successfully resolved and the identities of

279 The structures of the obtained isomers were then established using single crystal X-ray

280 Only branched (br-) isomers were transformed generating F(-) (no SO4(2-)) an

281 At 90 degrees C, 95% of br-PFOS isomers were transformed within 5 days.

282 d promotes the generation of chiral benzylic isomers, when combined with a Hantzsch ester as the redu

283 ns head-tail isomers and the trans head-head isomer, where the CHF group is defined as the TrFE "head

284 that permit the simultaneous discernment of isomers which differ in both the positions of acyl chain

285 aries contain both [2]catenanes and sequence isomers, which can be distinguished by HPLC-MS/MS.

286 Here we show that Lewis and blood group isomers, which have identical fragmentation spectra, exh

287 presence of ribose generated kinetin and its isomer, while its reaction with adenosine generated kine

288 radiation with 470 to 530 nm light and 99% Z isomer with 590 up to 680 nm light.

289 e S-E isomer in the case of MeQd and the R-E isomer with TMSQ catalysts.

290 lly stable under ambient conditions, and the isomer with two N-connected ligands was characterized by

291 in T1 energies are observed when going from isomers with linear connectivity of the fused benzene ri

292 devise an alternative approach resulting in isomers with the desired orientation of the nucleobase.

293 In this study we investigated 11 isomers with the molecular formula C6H13NO2 (m/z 131) to

294 orm field ion mobility for a narrow scope of isomers with variations in both bond coordination and st

295 of GeXIVA are more potent than the globular isomer, with low nanomolar half-maximal inhibitory conce

296 ntioseparation of E(R), Z(R), E(S), and Z(S) isomers, with a characteristic interconversion zone betw

297 s relative to their corresponding structural isomers, with the Fe, Co, and Ni variants showing more t

298 identification of cis and trans double-bond isomers within intact complex lipid mixtures using elect

299 multiple substitution degrees and positional isomers within the product.

300 selective formation of the ribbon disulfide isomer without requiring orthogonal protection.