ライフサイエンスコーパス: be prepared in

1 hibition binding affinity constant, 1.73 nM) was prepared in 1 step in a radiochemical yield of 14% +

2 isoquinoline alkaloid, (18) F-aspergillitine is prepared in 10 % isolated radiochemical yield from th

3 eochemistry and conformation as marineosin A was prepared in 11 steps from parasorbic acid.

4 Hapalindole J was prepared in 11% overall yield over 11 synthetic step

5 id (-)-hymenosetin and its N-methyl analogue were prepared in 11 and 8 steps, respectively, from (+)-

6 tities of the target drug candidates 1 and 2 were prepared, in 12 linear steps with 25% isolated yiel

7 (+)-Zincophorin methyl ester is prepared in 13 steps (longest linear sequence).

8 de ionophore bearing 14 stereogenic centers, is prepared in 14 steps (LLS).

9 14-membered macrolide 6-deoxyerythronolide B is prepared in 14 steps (longest linear sequence) and 20

10 Bromonaphthyridines are prepared in 15-65% yield via treatment of amidonapht

11 us, the all-cis 1,5,9-triene natural product was prepared in 15 steps from commercially available sta

12 co-polyethylene glycol diacrylate) monoliths were prepared in 150 microm i.d. capillaries using novel

13 C17-benzene ansamycins trienomycins A and F were prepared in 16 steps (longest linear sequence, LLS)

14 ring bryostatin analogue, macrodiolide WN-1, was prepared in 17 steps (longest linear sequence) and 3

15 d biocathode using graphene oxide (GO) could be prepared in 2 steps.

16 as in 2008, when 1,4-dimethoxypillar[5]arene was prepared in 22% yield, and subsequent improvements i

17 ld over 11 synthetic steps and hapalindole U was prepared in 25% overall yield over 13 synthetic step

18 The target compounds were prepared in 3-6 steps from commercially available s

19 Triethoxysilyl-substituted 1,3-butadiene has been prepared in 30-g quantities from chloroprene via a

20 The target compound 4-(11)C-MBZA was prepared in 46% +/- 7% radiochemical yields by react

21 Results: The target compound 4-(11)C-MBZA was prepared in 46% +/- 7% radiochemical yields by react

22 Thirty-six CH(4) in dry air PSMs were prepared in 5.9 L high-pressure aluminum cylinders

23 Tryptic digests were prepared in 50 mM formic acid and loaded onto the s

24 sphino)phenyl)morpholine (p-Mor-DalPhos, L2) was prepared in 63% yield and was crystallographically c

25 chiometric amount of template, ExBox(4+) can be prepared in 66% yield (following crystallization) usi

26 (III) siloxide [K(18c6)][U(OSi(O(t)Bu)3)4] 2 was prepared in 69% yield by reduction of [U(OSi(O(t)Bu)

27 he polyketide natural product cryptocaryol A is prepared in 8 steps via iridium catalyzed enantiosele

28 d tertiary alcohol benzoates and naphthoates were prepared in 81-99% yield.

29 The oxidant was prepared in 87% overall yield by combining a fluorou

30 carbons and one oxygen of the final product was prepared in 98.6% ee and 39% yield from cyclohexan-1

31 Spheres-on-sphere (SOS) silica particles are prepared in a one-pot scalable synthesis from mercap

32 The iodonium salts are prepared in a single pot from either commercially av

33 Complex structures are prepared in a single step using simple building bloc

34 The reported catalysts are prepared in a straightforward manner in two steps fr

35 , and the iridium-based photocatalyst 1a can be prepared in a 56% overall yield ( approximately 4.4 g

36 The Me(3)(OMe)tBuXPhos could be prepared in a chromatography-free manner from inexpen

37 etermining the number of dosage units (k) to be prepared in a composite sample of which there may be

38 Mixed-monolayer ERLs can be prepared in a few relatively simple steps using readi

39 P*, linear aldehydes with beta-chirality can be prepared in a highly enantioselective fashion with go

40 pCB can also be prepared in a hydrolyzable form as cationic pCB ester

41 They can be prepared in a large variety of shapes, with a host of

42 ass of neutral, monofluoroboronates that can be prepared in a one step, gram-scale fashion from readi

43 nge of highly functionalized enones can thus be prepared in a single operation in good yields.

44 finity purified IgG glycoprotein samples can be prepared in a single run with a liquid handling platf

45 and a variety of substituted aryl groups can be prepared in a single step from a simple mixture of am

46 Cyclopropyl malonoyl peroxide (1), which can be prepared in a single step from the commercially avail

47 elevant to neuroscience drug development can be prepared in a stereochemically comprehensive manner.

48 lactones obtained from marine sources, have been prepared in a concise and stereocontrolled manner f

49 es of anilines of industrial importance have been prepared in a continuous regime using this protocol

50 le alkaloids, 1, 2, and 3 respectively, have been prepared in a convergent manner by two related rout

51 enclosed by 24 high-index {720} facets, have been prepared in a monodisperse fashion by a modified se

52 y substituted pyrazolo[3,4-b]pyridines 4 has been prepared in a regioselective manner by the microwav

53 ne-substituted gamma- and delta-lactams have been prepared in a single step with high diastereoselect

54 bond and distinct heteroaromatic units have been prepared in a single step.

55 es [Ln(BH(4))(2)(THF)(2)] (Ln = Eu, Yb) have been prepared in a straightforward approach.

56 ane, in which all of the fluorines are 'up', is prepared in a 12-step protocol.

57 re, we describe a method in which the sample is prepared in a buffer at a lower concentration than th

58 compound is soluble in nonaqueous solvents, is prepared in a single synthetic step, has a low equiva

59 light absorber for solar fuel applications, is prepared in a wide compositional range.

60 [(76)Br]5 was prepared in a 51% +/- 19% radiochemical yield with h

61 The HSV-1 proteome was prepared in a flexible format for analyzing both CD8

62 plex containing pendant bithiophene moieties was prepared in a high-yield multistep procedure.

63 ',4'-difluoroarabinouridine (2,'4'-diF-araU) was prepared in a stereoselective way in six steps from

64 three building blocks, crude drug substance was prepared in a two-step sequence in high yield.

65 Samples were prepared in a 1-butyl-3-methylimidazolium bromide (

66 ric 2,5-diazabicyclo[2.2.2]octanes 14 and 15 were prepared in a chiral-pool synthesis starting from (

67 nm hollow gold nanoparticle superstructures were prepared in a direct one-pot reaction.

68 -Azabicyclo[3.1.0]hex-2-en-1-yl phosphonates were prepared in a five-step reaction route from beta-ke

69 ith a fragment of the bacterial 30S ribosome were prepared in a fully automated fashion and binding r

70 All meals were prepared in a metabolic kitchen.

71 All meals were prepared in a metabolic kitchen; breakfast and dinn

72 n-Alkyl arenes were prepared in a one-pot tandem dehydrogenation/olefin

73 methylsilyl)dicyclopenta[de,mn]tetracene (4) were prepared in a one-pot, palladium-catalyzed cross-co

74 MD fractions were prepared in a series of low-pressure stages where r

75 When these fermionic molecules were prepared in a single quantum state at a temperature

76 O-(alpha-Bromoacyl) cyanohydrins were prepared in a single step from a range of different

77 nds with a quaternary center (at C-2 or C-5) were prepared in a stereoselective fashion by engineered

78 Chiral spirocylic oxaphospholenes were prepared in a three-step sequence from chiral pool

79 The title compounds were prepared in a two-step sequence from 4,4-dimethoxyb

80 cid (3-MPA) capped lead sulfide quantum dots were prepared in a variety of organic solvents stabilize

81 This review is prepared in accordance with the PRISMA (Preferred Rep

82 The meta-analysis was prepared in accordance with Preferred Reporting of S

83 ade in this study would help the researchers be prepared in advance to deal with the challenges.

84 lternative for cellular therapy, as they can be prepared in advance, screened for pathogens and activ

85 are stable during long-term storage and can be prepared in advance.

86 sk performance often improves when tasks can be prepared in advance.

87 Solid supported fullerene materials are prepared in aims of creating a fullerene-based photo

88 c disordering and a high reversible capacity is prepared in air.

89 All solutions are prepared in an aqueous buffer without the addition o

90 ly tunable chiral Clickphine P,N-ligands has been prepared in an enantioselective fashion by Cu(I)-ca

91 (11)C-LY2795050 was prepared in an average yield of 12% and greater than

92 mples of various natural colouring solutions were prepared in aqueous model matrices at a range of pH

93 The honey slurries were prepared in aqueous solution containing hydrogen pe

94 organic nanoparticles (NPs) of the Spiro-BTA were prepared in aqueous solution.

95 Silver nanoparticles were prepared in aqueous solutions of chiral supramolecu

96 Abeta standards were prepared in artificial CSF containing 5% rat plasma

97 The polymer mounts were prepared in batches of 49 in 1 h 15 min, which allo

98 cobinamide solution for filter impregnation is prepared in borate-buffer rather than in water.

99 4-benzenedicarboxylic acid (bdc) linkers can be prepared in both interpenetrated and noninterpenetrat

100 ndrical cavities (4-mm diameter, 2-mm depth) were prepared in bovine incisors and restored using Bond

101 Cavities (4 x 2 mm) were prepared in bovine incisors and restored using Clea

102 Graphene nanoribbons (GNR), can be prepared in bulk quantities for large-area applicatio

103 It has now been prepared in bulk for the first time in THF solution

104 tetrasubstituted N-confused porphyrins (1-3) were prepared in ca. 3-5% yields using a [2 + 2] synthes

105 icative components from four unique species, were prepared in ca. 70% isolated yields and fully chara

106 ate-co-ethylene dimethacrylate) columns have been prepared in capillaries ranging in inner diameter f

107 ese interactions, a set of model DNA hybrids was prepared in conformations that ranged from end-tethe

108 of 1alpha,25-dihydroxy-19-norvitamin D have been prepared in convergent syntheses using the Wittig-H

109 eactions involving multiple reactants cannot be prepared in current microfluidic mixer designs, nor i

110 , unlike past methods, allows the protein to be prepared in defined conditions, free of excess deterg

111 (4-dihydroxymethylsilyl)butyl side chain has been prepared in enantiomerically pure form as a potenti

112 and oligoethylene glycol-derived spacers has been prepared in enantiomerically pure form.

113 zabicyclo[2.2.1]heptane-2-carboxylic acid 11 was prepared in enantiopure form, and its catalytic pote

114 s dramatically expand the materials that can be prepared in epitaxial heterostructures with precise i

115 f zeolite nanosheets (3 nm thick MFI layers) were prepared in ethanol following acid treatment, which

116 Primary alcohols were prepared in excellent yield from a variety of aliph

117 Dimethoxybenzitripyrranes were prepared in excellent yields by reacting benzene di

118 ated ynamides, a new type of building block, were prepared in excellent yields for the first time.

119 1,2-Disubstituted indolines have been prepared in fair to good yields by a Zn-mediated or

120 the gamma-secretase inhibitor LY411575, can be prepared in five steps from 2-bromophenylboronic acid

121 e, pentafluoroferrocene [Fe(C5F5)(C5H5)] can be prepared in five steps via a one-pot lithiation-elect

122 Each bacteriochlorin was prepared in five steps from an alpha-halopyrrole and

123 unds 12a-g and the (S)-prolinate analogue 13 were prepared in five steps from 2-nitrobenzoic acid (7)

124 H-imidazo[4,5-b]quinoline-9-carbonitriles 15 are prepared in four steps from N'-arylbenzamidines 11 a

125 luding indolizidines and quinolizidines, can be prepared in four steps from N-Boc beta-lactams.

126 The chiral auxiliary is prepared in four steps from N-Boc-L-tyrosine on a mul

127 2,2-Bis(azidomethyl)propionic acid was prepared in four steps and 85% yield from the commer

128 this case, an electron-rich aryl bromide 18 was prepared in four steps and subjected to palladium-ca

129 on of enantiopure 4-piperidone (-)-11, which was prepared in four steps from alpha-amino nitrile 6 th

130 Carrot and parsnips were prepared in four different forms (disc cutting, bat

131 Two iodoxanthones were prepared in four or five steps (33-50% overall yiel

132 These seven-membered-ring aza ketones are prepared in good yield with high enantiomeric excess

133 The synthetically versatile Michael adducts are prepared in good yields, with high levels of diaster

134 structurally diverse N-aryl heterocycles can be prepared in good to excellent yields under conditions

135 2-Substituted oxetan-3-ones can be prepared in good yields and enantioselectivities (up

136 2-Substituted azetidin-3-ones can be prepared in good yields and enantioselectivities (up

137 2-Vinylchromanes can also be prepared in good yields and high enantiomeric puritie

138 eries of 2-iminoimidazolin-4-ones could also be prepared in good yields from the reaction of aryl iso

139 Dicarbamates can also be prepared in good yields via the mild dehydration of t

140 ylic, aryl, and heteroaryl substituents have been prepared in good to excellent yields (up to 99%).

141 of new (E) and (Z)-benzoyl-homoquinones have been prepared in good yield by the parent quinone-electr

142 ings threaded by a two-binding-site axis has been prepared in good yield from relatively simple organ

143 Several sulfinyl ketimines have also been prepared in good yields by extension of the reactio

144 ad spectrum of trifluoromethylated compounds was prepared in good to excellent yields using CF3 CO2 K

145 aborated tetracyclic core of rhodexin A, 23, was prepared in good yield and excellent selectivity usi

146 It was prepared in good yield, isolated by fractional conde

147 opure C,N-palladacycles (PIN-acac complexes) were prepared in good overall yield in three steps from

148 The desired 3-amino-1,2,4-triazoles (1) were prepared in good overall yield via two convergent r

149 deficient chiral hypervalent iodine reagents were prepared in good overall yields.

150 amino acids bearing hydrophobic side chains were prepared in good to excellent yield by treating N-a

151 henoxazin-3-one substrates 23c, 23d, and 23e were prepared in good to high overall yield and were sel

152 Multisubstituted tetrahydrofurans were prepared in good yield with good enantioselectivity

153 These porphyrinoids were prepared in good yields (35-50%) and display unusua

154 An array of C-aryl and C-vinyl furanosides were prepared in good yields and diastereoselectivities

155 alyst epoxypyrrolo[1,2-a]azepine derivatives were prepared in good yields and excellent diastereosele

156 N-alkyl sulfinamides with diverse structure were prepared in good yields and excellent enantioselect

157 variety of aryl-substituted pyrroloindolines were prepared in good yields and with high levels of ena

158 ))(n)CH(2)(R)OH, n = 1, 2, 3, R = H, Me, Ph) were prepared in good yields by selenative demetalation

159 Potassium trifluoroboratoketohomoenolates were prepared in good yields from either the correspondi

160 Mg nanocrystals of controllable sizes were prepared in gram quantities by chemical reduction o

161 r ethyl trideca-2,4,6-trienoate (23-30) have been prepared in >/= 98% overall selectivity.

162 ,4E,6E)- and (2Z,4E,6Z)-trienoic esters have been prepared in >/= 98% selectivity by a newly devised

163 oisomers (7-10) of ethyl undeca-2,4-dienoate were prepared in >/= 98% isomeric purity by Pd-catalyzed

164 ,5]imidazo[1,2-c]quinazoline-6-carbonitriles are prepared in high yields via three new routes: (1) a

165 tituted vinylaluminum reagents, which cannot be prepared in high efficiency through direct reaction w

166 The two key building blocks can be prepared in high yield from commercially available st

167 -dihydro-2-vinyl-2H-1,4-benzoxazines (3) can be prepared in high yields (90-98%) and excellent enanti

168 A broad scope of aryl iodides can be prepared in high yields at room temperature under exc

169 s, highly substituted 1-naphthalenones could be prepared in high yields of up to 91%.

170 H14 )SnBr4 and 0D (C4 N2 H14 Br)4 SnBr6 can be prepared in high yields.

171 dazo[1,2-a]pyridine (alpidem derivative) has been prepared in high chemical yield through a unique pr

172 Diporphyrinbenzyloxy-BODIPY derivatives have been prepared in high yields, and the photophysical prop

173 romolecular chain transfer agent (macro-CTA) is prepared in high yield (>95%) with 97% dithiobenzoate

174 B, and C as well as its synthetic analogues was prepared in high chemical yield, from 27 to 91%, usi

175 The allylic silanolate salt was prepared in high geometrical (Z/E, 94:6) and high en

176 lkylated metallic nitride cluster fullerenes was prepared in high-temperature reactions and character

177 A series of alpha-quaternary arylglycines were prepared in high optical purity (up to 98% ee) by a

178 [(64)Cu]3-7 were prepared in high radiochemical yield (60-90%) and p

179 tricyclic and tetracyclic tetralin analogues were prepared in high yield and up to 20/1 diasteroselec

180 These new monomers were prepared in high yield by coupling of alkene-termin

181 Copolymers with benzothiadiazole were prepared in high yield by Suzuki polymerization to

182 [(99m)Tc(PS)2(Ln)] complexes were prepared in high yield in nearly physiologic condit

183 oles with desired N and O coordination atoms were prepared in high yield via click chemistry for pote

184 trans-2,8-Dioxabicyclodecanes were prepared in high yield with the creation of up to t

185 G) and cholesteryl alpha-d-galactopyranoside were prepared in high yield.

186 ne, and [(18)F]fluoroethyl-phenethyl-orvinol were prepared in high yields and quality from their 6-O-

187 es containing elevated levels of radiocarbon were prepared in-house and experimented with.

188 oil droplets after intravitreal bevacizumab was prepared in insulin syringes by a compounding pharma

189 The ligand was prepared in its protonated form by a three-step proc

190 er designs, but is far more accessible as it is prepared in just five steps and 23% overall yield.

191 ived from the abundant amino acid valine and are prepared in large quantities in four steps with inex

192 the known allylic alcohol (+)-14, which can be prepared in large quantities.

193 The new magnetic nanowire swimmers can be prepared in large scale using a simple template elect

194 Previously, compound 1 was prepared in low overall yield from piperidinone 2 vi

195 A variety of trisubstituted isoxazoles are prepared in moderate to excellent yields.

196 A variety of imidazolinone derivatives are prepared in moderate yields under mild conditions.

197 ,2,3-dithiazol-5-ylidene}methanes, these can be prepared in moderate yields via classical cycloadditi

198 Mannich artemisinin derivatives (7a-p) have been prepared in moderate to excellent yield.

199 inolines, furopyridines, and thienopyridines is prepared in moderate to excellent yields (up to 86%).

200 3-spiro[3-azabicyclo[3.1.0]hexane]oxindoles were prepared in moderate to high yields via one-pot thr

201 sly unknown, enantiopure, beta-amino ketones were prepared in modest yield by addition of lithium rea

202 ved from a robust heterocyclic salt that can be prepared in multigram quantities from inexpensive sta

203 and three [2,2']-paracyclophanes (pCps) has been prepared in multistep synthetic procedures involvin

204 nd 2-bromo-4-silacyclohexan-1-ones 5a and 5b were prepared in multistep syntheses, starting from trim

205 I) bromide in methanol, while 4-bromoketones are prepared in n-propyl acetate.

206 controlled length with low polydispersities were prepared in N,N-dimethylformamide using small seed

207 ew binary compound, Zn(8)Sb(7), has recently been prepared in nanoparticulate form via solution synth

208 s, a variety of functionalized anilines have been prepared in nearly quantitative yields within 2-8 m

209 5,5'-Disubstituted-3,3'-bisisoxazoles are prepared in one step by the dropwise addition of aqu

210 Versatile trichloromethyl carbinols can be prepared in one pot from primary alcohols by treatmen

211 pports with a hierarchical cross section can be prepared in one step by hollow fiber spinning, double

212 Our new ligand can be prepared in one step from commercially available star

213 y valuable substrate for drug discovery, can be prepared in one step from propargyl alcohol in a fair

214 zyl-2,4-dinitrobenzenesulfonamide (6), which is prepared in one step from commercial sources, had a p

215 weakly coordinating borate moiety (WCA-NHC) was prepared in one step from free N-heterocyclic carben

216 ide sheet with carboxyl-long-chains (GO-CLC) was prepared in one step from primitive graphite via Fri

217 n new 7'-homo-anhydrovinblastine derivatives were prepared in one or two steps from vinorelbine by me

218 A series of 2-acyl-5-aminooxazoles were prepared in one step.

219 cyclic fused and spiro-4-aminopyridines that are prepared in only three steps from commercially avail

220 These compounds are nonlabile, they are prepared in only two and three synthetic steps, resp

221 The natural alkaloid was prepared in only 13 steps, in an enantioenriched for

222 s (1,2-dienes) are inherently chiral and can be prepared in optically pure form.

223 planar chiral paracyclophane scaffolds have been prepared in optically pure form starting from 1,8-d

224 diluted" system with a 9:1 Co/Os metal ratio were prepared in order to further probe the nature of th

225 gs were radiolabeled and potent radioligands were prepared in order to image the beta-adrenergic and

226 structurally equivalent positions in FIV PR were prepared in order to study the molecular basis of P

227 Transcriptome libraries were prepared in parallel from the HPV18-positive HeLa c

228 the D-ring is annulated to the ABC-core, has been prepared in racemic form.

229 ic acid, an analogue of diaminopimelic acid, was prepared in racemic form and the structure establish

230 hexahydropyrazolo[1,5-a]pyridin-8-ium-1-ide, were prepared in seven steps from the respective commerc

231 The diarylamines were prepared in short, modular sequences from 2-aminopy

232 In each case, the target compounds were prepared in significantly fewer steps than previous

233 The methanesulfonate donors are prepared in situ from glycosyl hemiacetals, and are

234 he reactivity of these silyltriflates, which are prepared in situ, is exemplified by dipolar cycloadd

235 The catalyst is prepared in situ from commercially available reagents

236 These complexes were prepared in situ by reacting the compound [(dippe)N

237 il that yielded poly(HEMA-co-AEMA) foam that was prepared in-situ by UV crosslinking and by sequentia

238 P) natural product (+)-gliocladine C (6) has been prepared in six steps and 29% yield from the di-(te

239 analogue containing a diazirine moiety that was prepared in six steps and incorporated into an a-fac

240 e synthesis, the key building block 2, which was prepared in six steps from thiophene, was arylated r

241 102 adulterated samples were prepared in six batches with 17 replications for ea

242 3,4,9,10-bis(dicarboximide) conjugate (GPDI) was prepared in tetrahydrofuran.

243 When aggregates are prepared in the copresence of Cu(II) and Zn(II) ions

244 le and easy to use, provided the input files are prepared in the GraphML format, typically using the

245 Pure or doped graphene are prepared in the time of minutes and a thermal deoxyg

246 All movements are thought to be "prepared" in the brain before initiation, and prepar

247 methacrylate) diblock copolymer vesicles can be prepared in the form of concentrated aqueous dispersi

248 5-epi-7-epi-crassalactone D (15), also have been prepared in the course of the synthesis of (+)-cras

249 The hapten is prepared in the form of a stable prehapten through a

250 ReS2 is prepared in the form of flakes having thicknesses of

251 While PSA was prepared in the buffers to maintain an appropriate p

252 r sulfamethizole (SMZ) selective recognition was prepared in the form of a homogeneous thin film on t

253 The first synthetic molecular trefoil knot was prepared in the late 1980s.

254 size of the biocompatible PPy coating, which was prepared in the presence of cetyltrimethylammonium b

255 f FAs in the activity, a mixture of four FAs was prepared in the ratios measured in the dust samples

256 be feasible for creating a paste, and these were prepared in the laboratory.

257 Dynamic oligomers were prepared in the presence of CB[8], which acts as a

258 (La2O3), and Platinum (Pt) for Li-O2 battery are prepared in this study.

259 y immobilized (i.e., "locked") AVB analogues are prepared in this work.

260 couplings; a penta(piperidinone-piperidine) was prepared in this way.

261 elves have been recovered, each of which has been prepared in three dimensions.

262 The dialyzer is prepared in three stages: (i) disassembling the dialy

263 The compound is prepared in three steps from a simple carbenium precu

264 The key dehydrositagliptin intermediate 9 is prepared in three steps in one pot and directly isola

265 Dinemasone C was prepared in three steps (8% overall yield) from cis-

266 A key hydrindanone was prepared in three steps and 48% overall yield from c

267 g the 1, 2, and 3 positions methyl-protected was prepared in three steps from a commercially availabl

268 g 5% rat plasma, and quality control samples were prepared in three pooled CSF sources.

269 A series of 180 vinblastine 20' amides were prepared in three steps from commercially available

270 The complexes are prepared in two steps: (1) a one-pot reaction of pho

271 be commercially available from Aldrich, can be prepared in two steps using an abundant plant feedsto

272 = 2,2'-dihydroxy-1,1'-binaphthyl) groups has been prepared in two enantiomerically pure forms.

273 of perchlorate in water with dihydrogen have been prepared in two ways: (1) by impregnating 5 wt % Pd

274 Since 4-nitro-1-butanol in turn is prepared in two steps via Michael addition of nitrome

275 culate formulations of clopidogrel bisulfate were prepared in two crystal forms (Form I and Form II).

276 When these molecules were prepared in two different internal states or when m

277 Six rice bran oil (RBO) blends were prepared in two ratios i.e., 80:20 and 70:30 and an

278 of known heteroleptic iridium(III) complexes are prepared in up to 96% yield.

279 These pools are prepared in up to ~16% yield and 90-99% purity.

280 Neutral W-oxo-alkylidene-NHC catalysts can be prepared in up to 90% isolated yield.

281 nted by the spins of trapped ions, which can be prepared in various initial pure states.

282 uoromethylated oxygenated heterocycles could be prepared in very good yields through a single synthet

283 nthetase), and many disubstituted tRNAs have been prepared in vitro.

284 The shuttle plasmid carrying CCH1-GFP, which was prepared in vitro and propagated in yeast, was succe

285 ree conformationally distinct amyloid states were prepared in vitro using Syrian hamster recombinant

286 ore recently, a small range of complexes has been prepared in which alternative NHC isomers, namely i

287 rming photoinitiated substrate turnover have been prepared in which four different fluorotyrosines (F

288 A substituted TREN has been prepared in which the aryl groups in (ArylNHCH2CH2)

289 , a copper-based metal-organic framework has been prepared in which the starting linker (benzene-1,3,

290 Combinatorial scanning mutagenesis libraries were prepared in which CDR residues on the D5 light chai

291 R[N(SiMe3)2]3 R = -CH3, -C identical withCPh were prepared in which coordination of the hydrocarbyl g

292 tRNA synthetase pair, two PPARalpha variants were prepared in which Leu-258 or Phe-273 were site-spec

293 Perylene dyes with N-tert-alkyl substituents were prepared in which noncovalent interactions of the c

294 triphenylphosphine-gold(I) allenyl complexes were prepared in which the alpha carbon coordinates to t

295 To explore this possibility, BLM analogues were prepared in which the disaccharide moiety was attac

296 nucleophile assisting leaving groups (NALGs) were prepared in which the metal chelating unit is attac

297 importance of the thiophenyl moiety, analogs were prepared in which this moiety was replaced by an an

298 ns of geminal methyl and phenyl substituents were prepared in yields of 24-49% via dipyrromethane + d

299 ctionalized with the 5'-siloxyl ether linker were prepared in yields of 75-83% and incorporated last

300 oids pseudopalmatine and pseudoepiberberine, were prepared in yields up to 86% according to this stra