ライフサイエンスコーパス: enantiomer

1 strate the therapeutic potential of the R(+) enantiomer.

2 he tricyclic diastereomer from the (1 S,2 S)-enantiomer.

3 though Gce preferentially bound a natural JH enantiomer.

4 ms of the preferential formation of the ( R)-enantiomer.

5 evant pathway in the production of the major enantiomer.

6 quantification of each E and Z isomer of the enantiomer.

7 erence for the experimentally observed major enantiomer.

8 leaving the filtrate enriched with the other enantiomer.

9 all the desired activity comes from a single enantiomer.

10 e acceleration of more than 40 for the major enantiomer.

11 splayed more favorable kinetics toward the D-enantiomer.

12 arating (sub)micrometer-scale chiral crystal enantiomers.

13 racemates with a mixture of equal amounts of enantiomers.

14 response of the isostructural phen analogue enantiomers.

15 ssibilities for easy and fast analysis of AA enantiomers.

16 reened by chiral HPLC for resolvability into enantiomers.

17 igned the absolute configurations of the two enantiomers.

18 acrocyclic compound has been obtained as two enantiomers.

19 n enantioenriched form without resolution of enantiomers.

20 5]diazahelicene, enriched in (P,P)- or (M,M)-enantiomers.

21 ceptor binding behavior of the 2 radioligand enantiomers.

22 and a strong stereospecific preference for S-enantiomers.

23 nter will produce all four possible isobaric enantiomers.

24 ted at semipreparative level into their pure enantiomers.

25 e amenable to resolution into optically pure enantiomers.

26 exhibited similar turnover rates as their l-enantiomers.

27 -tetrapetalones A and C and their respective enantiomers.

28 CdTe QDs led to chiral recognition of these enantiomers.

29 ino sugars, 18 amino acids, and 4 amino acid enantiomers.

30 inactive state of D3R in complex with these enantiomers.

31 he first to generate these targets as single enantiomers.

32 kably more potent than the corresponding (R)-enantiomers.

33 .e., the change of the relative abundance of enantiomers.

34 ough for the satisfactory differentiation of enantiomers.

35 to potential existence of inactive and toxic enantiomers.

36 ents of chirality were synthesized as single enantiomers.

37 e almost perfect discrimination of their two enantiomers.

38 ls were measured to be different for the two enantiomers.

39 ere more potent than their corresponding (R)-enantiomers.

40 significantly higher tumor uptake than its D-enantiomer, 1-D-[(18)F]FETrp.

41 nd enantiopure samples revealed that the two enantiomers (1M and 1P) tend to narcissistically self-so

42 ne-resolved NMR signals are observed for the enantiomers (29 diverse analytes).

43 racemic mixture and ascertained that the two enantiomers (30a and 30b) are equiactive inhibitors for

44 The (R,R)-enantiomer 43 (PAT-1251) was selected as the clinical co

45 Enantiomer (-)-6 has been converted to potent HIV-1 prot

46 lective microbial processes favoring the (R)-enantiomer, a pronounced enantioselectivity favoring (S)

47 posite spiraling directions for the two PdGa enantiomers, a direct manifestation of the change of sig

48 In order to physically separate both enantiomers, a SPG derivatization with camphorsulfonic a

49 d the identification of the eutomer, the (S)-enantiomer, allowed to halve the dose totally relieving

50 Our study demonstrates that enantiomer and isotope fractionation of alpha-HCH are tw

51 lectric and magnetic dipoles associated with enantiomers and chiral plasmonic modes of CNAFs.

52 ormations: kinetic differentiation of allene enantiomers and desymmetrization of intermediate pai-all

53 emonstrate a work-flow for speciation of the enantiomers and diastereomers of 2-aminocyclohexanol as

54 h the understanding of assembly processes of enantiomers and racemates, in both dilute solution and c

55 paring the gelation propensity of individual enantiomers and racemates, we find that racemates of car

56 on that occurs between photoexcited D-/L-Trp enantiomers and rGO/gamma-CD giving rise to an enantiose

57 The mechanically planar enantiomers and their interconversion, arising from ring

58 full agonist according to the receptor, the enantiomer, and the signaling pathway investigated.

59 Both the natural d-enantiomer, and the unnatural and heretofore unknown l-e

60 rmance liquid chromatography (HPLC) into its enantiomers, and all four inherently chiral bambusuril p

61 rs: CycA and CycH (cyclosporin H), which are enantiomers, and isocyclosporin A (a structural isomer o

62 ors of Raman scattering (EFs) for particular enantiomers, and the SERS intensity was proportional to

63 rs of dimeric phenylpropanoyl-phloroglucinol enantiomers, (+)- and (-)-xanthchrysones A-C [(+)- and (

64 hat differ considerably in efficacy: the (R)-enantiomers are antagonists/weak partial agonists, where

65 While both Pai enantiomers are available, only one isomer is required-t

66 tivity relationship showed that (R)- and (S)-enantiomers are equally avid for GR by occupying discret

67 nists/weak partial agonists, whereas the (S)-enantiomers are much more efficacious.

68 Here, ten pairs of enantiomers are separated from the 19 structural isomers

69 ar mechanism identified the R(+)-propranolol enantiomer as a small molecule inhibitor of the SOX18 tr

70 permits isolating >50% of the (+)-ephedrine enantiomer as target compound in only 4 min.

71 e carboxylic acid, producing the same alkane enantiomer as that from the catalytic reaction.

72 ad to selectivity in the interaction between enantiomers based on their handedness.

73 The (R)-8 enantiomer bearing the chiral (alpha-methylbenzyl) was s

74 More intriguingly, neither of the two enantiomers binds specifically to human telomeric antipa

75 e abiotic processes usually act identical on enantiomers, biotic processes, such as biodegradation of

76 ciparum 80S ribosome with the (+)-mefloquine enantiomer bound to the ribosome GTPase-associated centr

77 e electrochemical discrimination between two enantiomers, but most importantly also allow stereospeci

78 ligand binding site induced by the bound (S)-enantiomers, but not by the (R)-enantiomers, that are fe

79 pene could be enhanced relative to the other enantiomer by the application of a sequence of microwave

80 16b, Ki = 24.3 nM] was resolved into its two enantiomers by chiral HPLC, and the absolute configurati

81 The Delta enantiomer, by contrast, is present in the structure but

82 han enantiopure compounds, and the mixing of enantiomers can enhance the aggregation propensity of pe

83 ived molecules for the preparation of single enantiomer compounds is an effective method to reduce th

84 [Cr(dqp)(2)](3+) and MM-(-)-[Cr(dqp)(2)](3+) enantiomers could be separated and isolated by using cat

85 We find that the unnatural enantiomer (D residues) displays cytotoxicity comparable

86 enabled separation and determination of 2HG enantiomers (D- and L-2HG) in frozen and FFPE tissues.

87 lectrical and optical mode for of tryptophan enantiomers (D-/L-Trp).

88 From the peptides designed, RR4 and its D-enantiomer, D-RR4, emerged as the most potent analogues

89 Herein we report that one metallohelix enantiomer Delta1a, available from a diastereoselective

90 The biological evaluation of both enantiomers demonstrated enantiospecific recognition at

91 idation affects antihistamine activity in an enantiomer-dependent fashion.

92 ype II E) are possible, leading to different enantiomers depending on the imine configuration (E- or

93 eer illustrated as relevant examples of each enantiomer determination.

94 nce is the tiny difference in energy between enantiomers due to parity violation in the weak force.

95 mer of fadrozole, and CYP11B1 binds to the S enantiomer, each with distinct orientations and interact

96 Each analyte enantiomer engenders a diastereomer with distinct fluore

97 -)-verticilide had no effect, its nonnatural enantiomer [ent-(+)-verticilide] significantly reduced R

98 icated for determination of thalidomide (TD) enantiomers (especially towards the toxic (S)-enantiomer

99 Its R-enantiomer evolved as a eutomer regarding PPARgamma acti

100 tructures with the addition of the Bay K8644 enantiomers exhibit similar inactivated conformations, s

101 otoswitches with chirality and the separated enantiomers exhibit tuneable chiroptical properties by p

102 es with mesomeric species, all of the tested enantiomers exhibited high SERS-ChA asymmetry factors (g

103 ave dose-limiting hepatotoxicity, 27 and its enantiomers exhibited limited off-target effects, result

104 at the transition state leading to the major enantiomer features a better steric fit and favorable pa

105 acemize the starting material and select one enantiomer for a highly enantioselective reaction.

106 hthol moiety (BINOL and VANOL), whereas diol enantiomers form complexes with the enantiopure amine-ty

107 A shift of the enantiomer fraction (EF) (-) from 0.50 to 0.35 in soil a

108 In the plume, the enantiomer fraction shifted up to 0.35, from 0.50 at sou

109 alpha-HCH), showed isotope fractionation and enantiomer fractionation during biodegradation.

110 tablished model for interpreting isotope and enantiomer fractionation patterns showed potential for a

111 ompound-specific isotope analysis (CSIA) and enantiomer fractionation.

112 dition, some of these reactions use a single enantiomer from racemic nucleophiles to afford stereopur

113 was achieved by selective adsorption of one enantiomer from the aqueous racemic mixture into the chi

114 combination with the ability to access both enantiomers from the carbene-catalyzed reaction is a pow

115 e and Cinchonidine epimers and amino alcohol enantiomers, from which the quantitative determination o

116 ed by single-isomer, and particularly single-enantiomer, fullerenes in organic electronic materials a

117 camphanic esters, achieving both enantiopure enantiomers (>99% ee) in 35% and 32% yields.

118 The enantiomers had opposite effects on oviposition preferen

119 ree synthesis of the natural product and its enantiomer has been achieved through the modified Knoeve

120 d host molecules for discrimination of guest enantiomers has been largely overlooked, which is surpri

121 The resolved metal-free 819 knot enantiomers have pronounced features in their circular d

122 We show that the enantiomers have similar binding affinities, but RR-RJW1

123 to produce each of the two possible product enantiomers (i.e., stereodivergence) of a new-to-nature

124 we determined that D-2HG is the predominant enantiomer in human breast tumors and show that the D-2H

125 is utilized to determine the amount of each enantiomer in the mixture with an error of <1% e.e. This

126 centers can be used to predict the er of the enantiomers in each diastereomeric set, along with the d

127 ranged triangular necklace 1 has two racemic enantiomers in its solid state with intriguing packing m

128 drug is responsible for racemic switch with enantiomers in presence of chiral environment for human

129 Detecting enantiomers in small quantities has an essential role in

130 ring between the inherently chiral AuNPs and enantiomers in the first filter holder, which results in

131 down to 2.5% with detection limits for the D enantiomers in the nanomolar range.

132 nantiomers (especially towards the toxic (S)-enantiomer) in blood plasma is still desirable.

133 onally dictating the assembly of mixtures of enantiomer (including racemates) is nontrivial.

134 Additional experiments with pure enantiomers indicated no interconversion.

135 However, binding of the l- and d-enantiomers induced different conformational changes of

136 tial spaces and preferential partitioning of enantiomers into SPs, which can be further enhanced by c

137 (ITC) show that the stronger binding of one enantiomer is accompanied by an increased gain in enthal

138 th intrinsic membrane-binding activity whose enantiomer is less potent than native peptide.

139 The other enantiomer is not a PAM, but it is an effective alloster

140 Selective separation of enantiomers is a substantial challenge for the pharmaceu

141 , the colorimetric discrimination of alanine enantiomers is examined and, more importantly, AuNPs-emb

142 20 and 23.6 nM, respectively] into their two enantiomers, isolating the affinity on the corresponding

143 fferent combinations of ligand and substrate enantiomers, it is now possible to access all four stere

144 In the case of an optically pure enantiomer, its absolute configuration can be determined

145 ost selective compound is a glucose-appended enantiomer, its cellular entry is not mainly glucose tra

146 strategy to interface native d-DNA with its enantiomer l-DNA-oligonucleotides of opposite chirality

147 gher brain biodistribution compared with its enantiomer L3.3, giving rise to stronger inhibition of A

148 One enantiomer may be active while the other inactive, alter

149 edicines was considerably higher than single enantiomer medicines.

150 are also active, while their corresponding d-enantiomers, methyl alpha-d-glucopyranoside 2,3,6-trisph

151 mechanism for how biomineralization-related enantiomers might exert hierarchical control to form ext

152 s selectively exerted by one of the two CpdX enantiomers, namely, CpdX(eA) or CpdX-D3(eA).

153 d a synthesis for optically active (d- and l-enantiomers) nonhydrolyzable analogs of 2-arachidonoyl-l

154 Overall, the 7R enantiomer of 71 (79) displayed more optimal efficacy, p

155 Specifically, the population of a specific enantiomer of a chiral terpene could be enhanced relativ

156 we describe an enantiospecific route to one enantiomer of a common decalin core that is present in n

157 ompared the properties of B-973B, the active enantiomer of B-973, with those of GAT107 regarding the

158 suppresses C-C bond formation with the l-G3P enantiomer of d-G3P.

159 Interestingly, the presence of only one enantiomer of each product was observed, indicating the

160 nating the heme iron, CYP11B2 binds to the R enantiomer of fadrozole, and CYP11B1 binds to the S enan

161 suggest that xestocyclamine A is in fact the enantiomer of ingenamine (+)-3.

162 intranasal formulation of esketamine, the S enantiomer of ketamine, in conjunction with an oral anti

163 An enantiomer of nabscessin A (1), an aminocyclitol amide w

164 orted d-allo-ShK was in fact d-ShK, the true enantiomer of natural l-ShK toxin, and that the apparent

165 erence for the ( R)-enantiomer over the ( S)-enantiomer of PEA-HCl.

166 methods used, experimental data for the (-)-enantiomer of tert-butylphenylphosphinoamidate were meas

167 S-BINOL induced formation of the other enantiomer of the cage selectively.

168 lows convenient access to either the R- or S-enantiomer of the chiral amine products in high yields a

169 Additionally, when a single enantiomer of the chiral dearomatization agent was used,

170 Furthermore, one enantiomer of the chiral MFDT exhibits faster knockdown

171 rentially utilized the naturally occurring l-enantiomer of the ether analog of lysophosphatidylcholin

172 The desired enantiomer of the final allylic amine can be synthesized

173 folds, and notably (-)-ent-quiannulatene, an enantiomer of the fungal metabolite (+)-quiannulatene.

174 de novo synthesis of l-NBDNJ (the unnatural enantiomer of the iminosugar drug Miglustat) and a preli

175 asymmetric synthesis of (-)-arborisidine, an enantiomer of the natural substance.

176 the chiral NDI receptor and the thalidomide enantiomer of the opposite configuration.

177 talyst could also be tuned to provide either enantiomer of the organoborane products.

178 chemical preference to dictate the preferred enantiomer of the reaction product.

179 ng stoichiometric amounts of the (+)- or (-)-enantiomer of the scarcely available and expensive diami

180 A carbohydrate-based synthesis of the enantiomer of the structure proposed for diplopyrone has

181 We show that one enantiomer of the TQS analog Cis-trans-4-(2,3,5,6-tetram

182 may be applied to (S)-carvone to afford the enantiomer of this common intermediate for other applica

183 igate the performance characteristics of the enantiomers of (11)C-Me-NB1, a recently reported PET ima

184 ed assay for determining e.e. in mixtures of enantiomers of 1,2- and 1,3-diols, chiral amines, amino

185 We isolated the enantiomers of 2,3,5,6TMP-TQS and determined that the (-

186 Short gram-scale syntheses of both enantiomers of 2-amino-3-hydroxycyclobutane-1-carboxylic

187 Enantiomers of 2-methylbutyl acetate were assayed in red

188 The study of the enantiomers of 3b and the corresponding tertiary amine 3

189 eved through the new approach to access both enantiomers of 4,5-di-O-benzyl-myo-inositol, derived fro

190 teps and 22% overall yield by employing both enantiomers of a BINOL-derived chiral phosphoric acid (C

191 me a valuable tool with which to access both enantiomers of a broad range of chiral arylaliphatic aci

192 ative populations of two otherwise identical enantiomers of a large gas-phase molecule using resonant

193 ical physical and chemical properties of the enantiomers of a molecule.

194 By switching the achiral proton source, both enantiomers of a series of tertiary alpha-aryl-1-indanon

195 nantiodivergent catalyst pair delivering the enantiomers of alpha-functionalized aldehyde products in

196 In this assay, enantiomers of amines and amine derivatives assemble wit

197 Fluorescent probes that can discriminate enantiomers of amino acids in organic media or aqueous s

198 polymers were treated with a mixture of the enantiomers of an amino alcohol, no fluorescence enhance

199 d by using a Cyclosil B column, on which the enantiomers of camphor, menthone, piperitone and carvone

200 The enantiomers of conjoined bis[5]diazahelicene and its dir

201 The optically pure enantiomers of heptahelical coumarins exhibit helicity-d

202 Despite their general absence in nature, the enantiomers of natural products may harbor unprecedented

203 3,5,6TMP-TQS isomers and active and inactive enantiomers of other TQS-related compounds identify the

204 Also, this work confirms that both enantiomers of the benzoin products can be accessed when

205 This allowed for the preparation of both enantiomers of the bicyclic product with near-identical

206 Attempts were made to resolve enantiomers of the chosen oximes on chiral GC columns.

207 that reacts at different rates with the two enantiomers of the electrophile, which interconvert unde

208 were developed to give enantiopure R- and S-enantiomers of the four lead compounds.

209 The enantiomers of the inhibitor could be resolved, and each

210 The P and M enantiomers of the octanuclear [Fe(8) (mu(4) -O)(4) (mu-

211 nt radical 1,5-C-H amination, producing both enantiomers of the strained five-membered cyclic sulfami

212 Through permutations of the enantiomers of the two chiral catalysts, all four stereo

213 Although both enantiomers of this compound have sub-micromolar IC(50)

214 Both enantiomers of this inhibitor of cytochrome P450 (P450)

215 on of a racemic intermediate to provide both enantiomers of this unusual bicyclic monosaccharide.

216 ridine with an equimolar mixture of opposite enantiomers of trans-1,2-diaminocyclopentane and trans-1

217 The syntheses of the enantiomers of two other closely related natural product

218 the work published on the adsorption of pure enantiomers, of enantiomeric mixtures, and of prochiral

219 When combined with the S enantiomer only, however, the achiral unit assembled in

220 lity status (either racemates, single active enantiomer or achiral) of medicines circulated on the ma

221 When used in a single-enantiomer organic field-effect transistor, the potentia

222 all hosts exhibit a preference for the ( R)-enantiomer over the ( S)-enantiomer of PEA-HCl.

223 voted to understanding how enrichment of one enantiomer over the other might have emerged from a preb

224 ost T3 showed certain selectivity toward one enantiomer over the other.

225 cells 100 times more effectively than the S enantiomer (P2-6S).

226 ce in both biotic and abiotic samples (seven enantiomer pairs d/l-Ala, -Asp, -Glu, -His, -Leu, -Ser,

227 specialist herbivore to linalool depends on enantiomer, plant genotype, and environmental complexity

228 However, the chain is helical, with only one enantiomer present, resulting in a chiral, noncentrosymm

229 peutic consisting of the pure cationic lipid enantiomer R-1,2-dioleoyl-3-trimethyl-ammonium-propane (

230 The enantiomer (R)-MDIMP [methyl (R)-2-(1,3-dihydroisoindol-

231 (+/-)Modafinil ((+/-)MOD) and its R-enantiomer (R-modafinil; R-MOD) have been investigated f

232 ith agonist activity led to the finding that enantiomers (R,R)-68 and (S,S)-68 have differential effe

233 l tetrasubstituted alkenes, undergo CAH with enantiomer ratios (er) as high as 99:1.

234 tivity values reaching greater than 20:1 and enantiomer ratios reaching up to 98:2.

235 ors, optoelectronic integrated circuits, and enantiomer-recognition sensors.

236 d 559 (26%) were racemates and single active enantiomers, respectively.

237 cific recognition at A2BAR, with the (S)-16b enantiomer retaining all the affinity (Ki = 15.1 nM), as

238 Moreover, separated cis enantiomers revealed Lambda-cis to have a preference for

239 158 muM; CVX, IC50 = 11 muM) than any of its enantiomers S (6c) (collagen, IC50 = 25.3 muM; CRP-XL, I

240 -Bay K8644, and a titration of its agonistic enantiomer (S)-(-)-Bay K8644 at resolutions of 2.9-3.4 a

241 cally expressing linalool synthases for both enantiomers, (S)-(+)- and (R)-(-)-linalool, reported to

242 ectable levels of self-disproportionation of enantiomers (SDE) during chromatography on an achiral st

243 Results showed variable enantiomer selectivity over the time course.

244 In contrast, constant enantiomer selectivity was observed in experiments emplo

245 From the 21 AAs studied, enantiomer separation was achieved for 17 AAs with mobil

246 G@SeNPs modified with different enantiomers show opposite handedness with a tunable circ

247 with fluorescently labeled analogues of the enantiomers showed their colocalization in racemic fibri

248 stically self-sort in the dimer regime, each enantiomer showing a strong preference to associate with

249 d to be a racemic mixture of the (R) and (S) enantiomers, so it has been unclear whether one or both

250 The enantiomer-specific activity and straightforward chemica

251 However, enantiomer-specific effects on receptor activation are p

252 Toxicity tests proved strong enantiomer-specific toxicity in the case of Tetrahymena

253 were unresolvable in a mixture, whereas the enantiomers studied did not exhibit statistically differ

254 Structures of AAD-1, an (R)-enantiomer substrate-specific enzyme, in complexes with

255 conformational changes of FliY, where the l- enantiomer-substrate-binding protein complex interacted

256 Additionally, we evaluated the (-)-JQ1 enantiomer that is structurally incapable of inhibiting

257 he bound (S)-enantiomers, but not by the (R)-enantiomers, that are features of partially activated re

258 ultrasonication increased levorotatory rutin enantiomers, that can be used to further modify physico-

259 Also, ADCs with a nonprotease-cleavable enantiomer, the VC(R) isomer, mediated effective cell ki

260 route was designed to enable access to both enantiomers, the absolute configuration of the natural p

261 accelerating the transformation of the major enantiomer through attractive non-covalent interactions

262 kinetic differentiation of the cyclic allene enantiomers through stereoselective olefin insertion, lo

263 The mixing of Abeta42 enantiomers thus accelerates the formation of non-toxic

264 ence quenching due to the tendency of chiral enantiomers to form complexes with gamma-CD in different

265 We showed that J113863 and its enantiomer UCB35625, initially identified as high affini

266 -oxazolidine-2-one, was resolved into single enantiomers using a chiral auxiliary to access enantio-e

267 rium product distributions between substrate enantiomers using excited-state redox events.

268 x formed from them, have been separated into enantiomers using HPLC with a chiral stationary phase.

269 (13)C NMR signals of the two nanostructured enantiomers vanished.

270 sted that the preferential transformation of enantiomers varied at different growth stages.

271 nsferring information between orthogonal DNA enantiomers via an achiral intermediary, opening the doo

272 llenging to obtain these compounds as single enantiomers via the established synthetic procedures due

273 ute configuration of the more slowly eluting enantiomer was established by X-ray crystallography.

274 In certain cases, the opposite enantiomer was favored (up to 4:96 er).

275 y factor since degradation of the individual enantiomers was biphasic in itself.

276 The presence of two enantiomers was demonstrated performing NMR enantiodiffe

277 ved when a 2:1 ratio of R and S subcomponent enantiomers was employed.

278 pecific rotation of tetrafluoro[6]helicene 6 enantiomers was found to be approximately 25% lower than

279 The migration order of the DL enantiomers was found to be dependent on the structure o

280 e enhancement was observed unless one of the enantiomers was in excess of the other.

281 Chiral amplification within M(3)L(3) enantiomers was observed when a 2:1 ratio of R and S sub

282 the binding orientation of all (R)- and (S)-enantiomers was revealed.

283 By comparing two enantiomers, we observe a reversal of their Fermi-arc ve

284 nantiomerically pure natural product and its enantiomer were prepared in seven steps and 22% overall

285 Both enantiomers were accessible from the same precursors by

286 Hyperpolarized (13)C-labeled dl-methionine enantiomers were differently observed with a single-scan

287 n slightly acidic soils, differences between enantiomers were not pronounced, and in strongly acidic

288 mprove its aqueous solubility, 5 and its two enantiomers were synthesized and converted into their co

289 benzo[d]azepin-1-ol ((11)C-NR2B-SMe) and its enantiomers were synthesized as candidates for imaging t

290 Individual pure enantiomers were then selectively heart-cut from within

291 , and the unnatural and heretofore unknown l-enantiomer, were converted to disaccharide derivatives c

292 have synthesized the highly active (-)-KF116 enantiomer, which displayed EC(50) of ~7 nM against wild

293 CPPL was resolved into enantiomers, which are configurationally stable and prov

294 suggested a specific interaction of the (-) enantiomer with alpha7T106, and allosteric activation of

295 ure can be transformed into an excess of one enantiomer with the aid of chiral auxiliaries, but has b

296 ge, this is the first example of one pair of enantiomers with contrasting selectivity for human telom

297 ved through the self-assembly of alternating enantiomers with hydrogen bonds as the intermolecular dr

298 aturing three stereocenters was a mixture of enantiomers with no other diastereomers observed.

299 ivatives (12d, 13c, and 14c) provided single enantiomers with significant enantioselectivity in HIV-1

300 namically isomerize, interconverting between enantiomers without cleavage of a constituent bond, nor