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 lopentane-1-carboxylic acid ([(18)F]28) have been prepared in 10 and 1.7% decay corrected radiochemic

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

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

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

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

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

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

9 and the majority of the stereogenic centers, was prepared in 13 linear steps (longest sequence) in 8%

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

11 14-membered macrolide 6-deoxyerythronolide B is prepared in 14 steps (longest linear sequence) and 20

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

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 (-)-Himeradine A was prepared in 17 steps in the longest linear sequence.

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

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

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

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

20 Standards were prepared in 4% albumin solutions and compared again

21 ctly from commercial materials, 10 analogues were prepared in 41-96% yields in one step.

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

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

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

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

26 The dioxinone keto ester 12 was prepared in 6 steps from geraniol using allylic func

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

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

29 (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)

30 0-membered marine macrodiolide clavosolide A is prepared in 7 steps (LLS) in the absence of protectin

31 e first amino acid-Fmoc-O-TIPS-beta-tyrosine-was prepared in 78% yield (two steps in one pot).

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

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

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

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

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

37 The monomers are prepared in a short and divergent synthetic sequence

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

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

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

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

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

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

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

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

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

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

48 eight star and dendritic block copolymers to be prepared in a single step under ambient conditions.

49 ing up to three contiguous stereocenters can be prepared in a single step.

50 nic, non-toxic analogue of ibogaine that can be prepared in a single step.

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

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

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

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

55 n, a series of donor-sigma-acceptor dyes has been prepared in a modular approach.

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

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

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

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

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

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

62 Biotin-l-sulfoxide[6]uril is prepared in a highly diastereoselective one-pot synth

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

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

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

66 A neutral tetralactam macrocycle was prepared in a few minutes in one pot and at high con

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

68 ',4'-difluoroarabinouridine (2,'4'-diF-araU) was prepared in a stereoselective way in six steps from

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

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

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

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

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

77 iaza[5]helicenes with different substituents were prepared in a straightforward manner through indole

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 ium content levels (ca. 6.5-30 mg Ca/100 kJ) were prepared in accordance with the guidelines of Commi

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

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

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

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

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

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

90 Moreover, it can be prepared in an extremely high humidity atmosphere and

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

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

93 te-specifically derivatized with sialic acid were prepared in an overall yield of 50-60%.

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

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

96 Silver nanoparticles were prepared in aqueous solutions of chiral supramolecu

97 WPI solutions were prepared in aqueous solutions with different concen

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

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

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

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

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

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

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

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

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

107 A total of 80 osteotomies were prepared in dense bone samples (quality Type II) by

108 nt beds (i.e., narrow and standard diameter) were prepared in each of 36 porcine bone blocks.

109 (4-dihydroxymethylsilyl)butyl side chain has been prepared in enantiomerically pure form as a potenti

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

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

112 lfanylindolizines and 2 1-selanylindolizines were prepared in excellent yields by an intramolecular a

113 Dimethoxybenzitripyrranes were prepared in excellent yields by reacting benzene di

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

115 1,2-Disubstituted indolines have been prepared in fair to good yields by a Zn-mediated or

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

117 ral acylpyruvate derivative, which, in turn, is prepared in five steps from commercially available ma

118 ne lignans from a common intermediate, which is prepared in five steps from known materials.

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

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

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

122 hus, tetrahydro-5 H-benzo[ c]fluorenes could be prepared in four steps from appropriately substituted

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

124 2,2-Bis(azidomethyl)propionic acid was prepared in four steps and 85% yield from the commer

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

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

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

128 Six-membered cyclic carbamates are prepared in good yield with high levels of enantiose

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

130 2-Substituted azetidin-3-ones can be prepared in good yields and enantioselectivities (up

131 2-Substituted oxetan-3-ones can be prepared in good yields and enantioselectivities (up

132 2-Vinylchromanes can also be prepared in good yields and high enantiomeric puritie

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

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

135 ral, and a variety of aryl O-glycosides have been prepared in good to excellent yields.

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

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

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

139 (11)C-EKAP was prepared in good radiochemical purity.

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

141 of N-substituted 7-amino coumarin analogues was prepared in good to excellent yields.

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

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

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

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

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

147 ng bulky o-biphenyl or m-terphenyl fragments were prepared in good to excellent yields.

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

149 for a wide array of target hydrazones, which were prepared in good to high yields under smooth reacti

150 Multisubstituted tetrahydrofurans were prepared in good yield with good enantioselectivity

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

152 timized reaction conditions, chiral benzoins were prepared in good yields (up to 83%) and excellent e

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

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

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

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

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

158 vailable substrates, 39 examples of products were prepared in good yields with outstanding functional

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

160 ,5]imidazo[1,2-c]quinazoline-6-carbonitriles are prepared in high yields via three new routes: (1) a

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

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

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

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

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

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

167 tives that possess three chiral centers have been prepared in high yield and stereocontrol from silyl

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

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

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

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

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

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

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

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

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

177 [(99m)Tc(PS)2(Ln)] complexes were prepared in high yield in nearly physiologic condit

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

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

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

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

182 new system, and the pharmaceutical ibutilide was prepared in higher yield and under milder conditions

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

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

185 veral stable dibenzonorbornadienones 41 have been prepared in just two steps starting from anthracene

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

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

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

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

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

191 ionally, 4-bromo- and 4-iodoisocoumarins can be prepared in moderate to good yields by replacing NCS

192 ,2,3-dithiazol-5-ylidene}methanes, these can be prepared in moderate yields via classical cycloadditi

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

194 isting of new polyaminoisoprenyl derivatives were prepared in moderate to good chemical yields varyin

195 3-spiro[3-azabicyclo[3.1.0]hexane]oxindoles were prepared in moderate to high yields via one-pot thr

196 er pyrazole-based bis-heterocyclic molecules were prepared in moderate to high yields.

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

198 the base 1,2-benzothiazine 1,1-dioxides can be prepared in most cases as the main product, in a diaz

199 is needed for the second catalytic step can be prepared in multigram quantities from inexpensive sta

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

201 Diamine (-)-1 has been prepared in multigram quantities from the known bic

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

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

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

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

206 ite (topology type MER) with Si/Al = 3.8 has been prepared in Na, K, and Cs forms and its structural

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 new zeolite structures, the OSDAs for EMM-17 are prepared in one simple alkylation step, making EMM-1

210 5,5'-Disubstituted-3,3'-bisisoxazoles are prepared in one step by the dropwise addition of aqu

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

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

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

214 llows functionalized gamma-butyrolactones to be prepared in one step from simple tertiary alcohol-der

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

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

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

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

219 Finally, highly substituted gamma-lactams were prepared in one pot from adducts obtained using ace

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

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

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

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

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

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

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

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

228 The fungal metabolite illudinine is prepared in seven steps and ca. 55% overall yield fro

229 ally pure natural product and its enantiomer were prepared in seven steps and 22% overall yield by em

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 H(2)CO(3)* eluent is prepared in situ by high pressure permeative introduc

236 The catalyst is prepared in situ from commercially available reagents

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

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

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 nt matrix-effect was verified, and standards were prepared in solvents.

243 A wide variety of graphs can be prepared in TBtools using a new plotting engine ("JIG

244 3,4,9,10-bis(dicarboximide) conjugate (GPDI) was prepared in tetrahydrofuran.

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

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

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

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

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

250 The samples can be prepared in the form of pellets of 13 mm in diameter

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

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

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

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

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

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

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

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

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

260 limiting the scope of nanomaterials that can be prepared in these ways.

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

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

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

264 ns, twenty-eight (28) heteroarylated ketones were prepared in this study to demonstrate the substrate

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

266 The present article has been prepared in three main categories.

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

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

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

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

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

272 ctional diaryl- and diheteroarylzinc species were prepared in toluene within 10 min to 5 h through an

273 ural and starter culture fermented cucumbers were prepared in triplicate in sodium chloride brines an

274 Samples and calibration standards were prepared in Tris buffer (pH:7.2) for selective hydr

275 uced the latency at which habitual responses were prepared, in turn increasing the likelihood of thei

276 The new CSAs are prepared in two steps from Lambda-(S,S)-1(3+) 3Cl(-)

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

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

279 = 2,2'-dihydroxy-1,1'-binaphthyl) groups has been prepared in two enantiomerically pure forms.

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

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

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

283 NMR samples were prepared in two types of commercially available sam

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

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

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

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

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

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

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

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

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

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

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

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

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