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1 carbon crystal, different from graphene, has been prepared from 1,3,5-trihydroxybenzene, consisting o
2 hene) functionalized with four heptyl groups is prepared from 1,8-dibromo-4,5-diheptylbenzo[1,2-b:4,3
6 ood and a fifth card from finger-prick blood were prepared from 103 HIV patients with a median viral
8 tituted 3-azabicyclo[3.1.0]hexan-2-ones have been prepared from 2-iodocyclopropanecarboxamides by a t
11 urea and thiourea derivatives of vinblastine were prepared from 20'-aminovinblastine that was made ac
13 yrrol-3-yl)-1H-1,2,4-triazol-4-ium bromides, were prepared from 2H-azirines and triazolium phenacyl b
14 yes as probes, a turn-off fluoride ion probe was prepared from 3C, which consisted of a silyl ester r
15 Polymeric nanoparticles having Pt(IV) ion were prepared from (4-Formyl-3-methoxyphenoxymethyl) pol
21 ion of the corresponding benzyl alcohol) but are prepared from a common key intermediate, the C(3)-tr
22 in that they adopt S = 3/2 ground states and are prepared from a four-coordinate, S = 3/2 trigonal py
23 well as their corresponding monoalkyl esters are prepared from a pivotal intermediate epoxide 12.
29 nse number of multivariate MOF materials can be prepared from a small collection of molecular buildin
30 oxoiron(IV) complex is now reported that can be prepared from a well-characterized oxoiron(III) speci
31 ally occurring hyacinthacines B1 and B2 have been prepared from a common, easily available, advanced
32 n of a dihydrodipyrrin-acetal, which in turn is prepared from a 2-(2-nitroethyl)pyrrole species and a
36 g a simple and robust catalyst system, which is prepared from a salen complex and an onium salt, this
39 sponge-derived alkaloid dibromoagelaspongin was prepared from a dihydrooroidin derivative by exploit
40 10,14-tetramethylhenicosan-1-ol TBDPS ether, was prepared from a late stage synthetic intermediate.
44 om 6,9-dichloro-5,10-diaza[5]helicene, which was prepared from a readily available quinoline building
45 alenes (IF-TTFs) with thioacetate end groups was prepared from a readily obtainable dibromo-functiona
48 (dried cubic pieces, dried powder) products were prepared from a homogenous mango fruit batch to obt
49 ries of fluorescent teraryls and quateraryls were prepared from a ketene-S,S-acetal under mild condit
50 ntain any organic structure-directing agents were prepared from a multilamellar MFI (ML-MFI) zeolite.
54 al 3,6-disubstituted 4-alkylaminopyridazines were prepared from a sequence of three chemo- and regios
56 hree-center, two-electron Au-H-Cu bonds have been prepared from addition of a parent gold hydride to
57 ue, slices containing the lateral OFC (lOFC) were prepared from adult C57BL/6J mice and whole-cell pa
60 is possible because beta-aminoaldehydes can be prepared from alpha,beta-unsaturated aldehydes by an
62 celles (SCMs) containing Co(III)-salen cores were prepared from amphiphilic poly(2-oxazoline) tribloc
65 , in which a homogeneous, flowing suspension is prepared from an inhomogeneous mixture of particulate
67 s including cone-, pencil-like, and stepwise are prepared from anodized aluminum oxide templates.
68 , but were inactive in such cells when these were prepared from Anx-A1 null mice or when the neutrali
73 Vinyl silyl ethers and disiloxanes can now be prepared from aryl-substituted alkenes and related su
79 of the 1,3,5-triol stereoisomers can easily be prepared from beta-siloxy methyl ketones in no more t
80 uisite peptides with heterogeneous backbones were prepared from beta-, gamma-, and delta-amino acids
81 ly characterised for their phenolic content, were prepared from bilberries (Vaccinium myrtillusL.) an
82 le nanotubes with a hydrophobic interior can be prepared from bottlebrush copolymers with triblock co
85 te that a range of difluorobenzodioxoles can be prepared from catechols in two steps through conversi
88 Herein, hexagonal boron nitride (h-BN) films are prepared from chemical vapor deposition (CVD) and re
92 ts was unknown, external calibration samples were prepared from chlorpheniramine maleate and microcry
93 yrmecin, teucriumlactone, and dolicholactone were prepared from citronellol using a divergent diaster
94 g an array of substituents at C2 that cannot be prepared from commercial beta-amino acids or by one-c
95 osphate and peracetylated GalNAc-1-phosphate are prepared from commercially available undecaprenol an
96 lly flexible furan-derived allocolchicinoids was prepared from commercially available colchicine in g
97 ous benzaldehyde tethers with a cyclic enone were prepared from commercially available 2-hydroxybenza
98 ch isotopically substituted bacteriochlorins were prepared from commercially available reactants (bac
100 milk only (Controls), and hippocampal slices were prepared from Control- and CNN-treated young adults
101 odels of diamond with surface sp(2)-defects, were prepared from corresponding ketones via a McMurry c
103 c nonclassical [Cp2ZrN(SiHMe2)2](+) ([2](+)) is prepared from Cp2Zr{N(SiHMe2)2}H (1) and B(C6F5)3 or
104 crystals (NCs) with tunable Cu stoichiometry were prepared from Cu-rich covellite (Cu1.1S) nanoplates
107 -ORM-13070 with (11)C-methyl triflate, which was prepared from cyclotron-produced (11)C-methane via (
108 ydrate side chain with D-ribo configuration, was prepared from D-glucose by inverting the C-3 stereoc
109 ,4-dideoxy-(1S)-pent-3-enopyranosid-2-ulose) was prepared from D-xylose, while the R analogue was obt
112 e-cell disaggregates from adult C57BL/6 mice were prepared from different tissues and tested for thei
115 al trial (combined model), and the other two were prepared from each location LCB and Efaw model.
117 ed a structurally diverse substrate scope to be prepared from either an isolated palladium-CF(3) comp
119 eres with unique structures and morphologies are prepared from energetic carbon precursors, alkali pr
124 ll library of 57 low molecular weight oximes was prepared from fragrant aldehydes and ketones, and th
129 is quite rare in natural plants, and it must be prepared from glycyrrhizin (GL) by hydrolysing one te
130 and high (0.092) degree of substitution (DS) were prepared from granular native waxy maize starch in
131 NC5H3](2-) (Ar = 2,6-diisopropylphenyl), can be prepared from H2[Ar2N3], butyllithium, and (t-BuO)3Mo
132 e construction of the reporter ion group can be prepared from halogenated alkyl groups which are also
133 Purified HBV particles on the whole, which were prepared from HBV DNA-positive and protein-rich fra
134 ,9S)- and (3S,5S,6S,9S)-I(2)aa diastereomers were prepared from hexahydro-1H-azonines by using iodine
136 sions of lead halide perovskite nanocrystals are prepared from high-quality lead halide nanocrystal s
138 re bench-stable, crystalline solids that can be prepared from inexpensive, commercially available alc
139 CBD), a fully synthetic analogue of CBD that is prepared from inexpensive, non-cannabis derived precu
140 this system, albumin nanoparticles (Alb NPs) were prepared from inherent biocompatible bovine serum a
145 in MICs, regardless of whether the inoculum was prepared from isolates grown in Middlebrook 7H9 medi
149 - or gamma-iodo amino acid derivatives which are prepared from L-serine or L-aspartic acid, respectiv
151 arbamate 9 and fused beta-lactam scaffold 11 were prepared from L-pyroglutamic acid via substrate-con
152 s of large, optically active Fe(4)L(6) cages was prepared from linear 5,5'-bis(2-formylpyridines) inc
153 arly clickable polymer-caged nanobins (PCNs) were prepared from liposome templates using a drop-in ch
157 mulsions with good oxidative stability could be prepared from marine PL of high purity and high conte
158 Various achiral and chiral Cu(I) salts have been prepared from mesitylcopper(I) and investigated for
164 ning short uranium-group 10 metal bonds have been prepared from monometallic IU(IV)(OAr(P)-kappa(2)O,
165 blished that oligosaccharide stannanes could be prepared from monosaccharide stannanes via O-glycosyl
167 ride and lithium diisopropylaminoborohydride are prepared from n-butyllithium and the corresponding a
168 -substituted 1,2,3,4-tetrahydroisoquinolines was prepared from N-(o-nitrophenylsulfenyl)phenylethylam
175 rystalline particles (Re NPs), of 2 nm size, were prepared from NH4ReO4 under mild conditions in neat
178 phenylsilyl (TBDPS) protecting groups at O-3 were prepared from p-methoxyphenyl d-galactopyranoside.
179 the DA levels of exogeneous DA samples that were prepared from PC12 cells by a DA release assay were
183 benzo[3,4]phenanthro[2,1-d]thiophene (BPBPT) was prepared from polyaryl thiophenes via regioselective
185 tificial two-dimensional biological habitats were prepared from porous polymer layers and inoculated
187 ons, Pt@Pb(1)(0)(-)(1) and Pt@Pb(1)(2)(1)(-) were prepared from "preassembled" clusters generated fro
193 n of pseudoephenamine glycinamide, which can be prepared from pseudoephenamine in a one-flask protoco
194 potential for nonspecific interactions that was prepared from purified bromelain glycopeptides and h
195 present study, GLT-1 immunoaffinity isolates were prepared from rat cortex using three strategies and
197 -4-MeC6H2)](H)( horizontal lineGeH(t)Bu) (8) was prepared from reaction of (t)BuGeH3 with the benzyl
198 inked carboxymethyl rice starches (CL-CMRSs) were prepared from reactions between native rice starch
200 e required enantiopure phenyl propanoid unit was prepared from readily available ( R)-methyl lactate.
201 A variety of aryl-alkyl and diaryl sulfides were prepared from readily available arylamines and aryl
202 s: Enantioenriched bicyclo[5.3.0]decatrienes were prepared from readily available chiral 3-acyloxy-1,
207 d their corresponding tetrahydrochlorides 11 were prepared from (S)- and (R)-2-methylpiperidine.
213 curacy whether a grasping or pointing action was prepared from signals in visual cortex as early as V
214 e of 9 min, the sodium salt of ciprofloxacin was prepared from simple building blocks via a linear se
217 ngle crystals of (3-pyrrolinium)(CdCl3 ) can be prepared, from solution, on top of aligned semiconduc
218 istry expands the scope of products that can be prepared from terminal alkynes by practical and high-
219 d hexaaryl-1,4-dihydropyrrolo[3,2-b]pyrroles were prepared from tetraaryl-1,4-dihydropyrrolo[3,2-b]py
220 anospheres with uniform size and composition are prepared from the co-reduction of palladium and silv
221 )2Rf8; b, (CH2)3Rf8; c, H (Rf8 = (CF2)7CF3)) are prepared from the corresponding phosphines 3a-c and
224 Both enantiomers of Garner's aldehyde (3) are prepared from the same alkene 4 by catalytic asymmet
226 in-2-ones and 6-(3-oxobutyl)piperidin-2-ones are prepared from the Wacker oxidation of internal alken
228 hesis of a C-linked mimic, C-GlcNAc Ser, has been prepared from the C-Glc Ser by a double inversion s
229 (F)] (2; t-BuPy = 4-tert-butylpyridine) have been prepared from the corresponding iodides and AgF.
230 :4,5]pyrrolo[1,2-c][1,2,3]benzotriazine have been prepared from the key intermediates 2-(1H-pyrrolo[2
231 ew series of 6 dimeric trioxane sulfones has been prepared from the natural trioxane artemisinin in f
232 lm device for second harmonic generation has been prepared from the nitro-substituted liquid crystall
234 pp-Imd-BH(2)X, X = halide or sulfonate) have been prepared from the parent borane dipp-Imd-BH(3) by (
235 antalum pentaazide with N-donor ligands have been prepared from the pentafluorides by fluoride-azide
236 ketone, nitrile oxide, or azide residues has been prepared from the precursor iodide 7 using Negishi
237 rium-labeled Ta(CD(2)Bu(t))(5) (1-d(10)) has been prepared from the reactions of (Bu(t)CD(2))(3)TaCl(
239 vine immunoglobulin G, herein termed EBOTAb, was prepared from the antisera and used for an in vivo g
242 piperazinyl)methyl H8BINOL compound, (S)-11, was prepared from the Mannich-type reaction of (S)-H8BIN
243 yl prodrug of the antitumor agent triptolide was prepared from the natural product in three steps (39
244 complex [Ru(II)(bpy)(2)(1)(2)](PF(6))(2) (2) was prepared from the nitrile-based peptidomimetic inhib
245 n addition, fully saturated poly-fused rings were prepared from the carboacylation products through a
246 nuronides singly labeled with (13)C at C1-C6 were prepared from the corresponding (13)C-labeled methy
248 Pseudococcus longispinus and its enantiomer were prepared from the corresponding bornyl acetates.
250 ents in meso-phenyls and anthracene residues were prepared from the corresponding pyrrolic precursors
254 = SiMe3), analogues of the Grubbs catalyst, were prepared from the dimer [Ru(mu-Cl){kappaP,P,Si-Si(M
256 rotein hydrolysates of profitable properties were prepared from the fodder potato protein concentrate
257 ap)4] (compounds 4k+2b with k = 2, 3, and 4) were prepared from the Glaser coupling reaction between
260 6 as well as (15S)-ethyl-nor-brefeldin A (2) were prepared from the key building blocks 12 or 24 by J
261 ee separate nitrogen-containing heterocycles were prepared from the N-acylguanidines synthesized usin
265 idges the quadruply bonded molybdenum atoms, were prepared from the reaction of the appropriate [Mo2{
267 mperate population, metagenomes of each type were prepared from the same seawater sample from Tampa B
268 nanoparticle superstructures with P-helicity were prepared from the sol form of the template through
270 ostructural, nonclassical Co(H(2)) complexes are prepared from their Co(N(2)) precursors using tris(p
272 ridgehead CF(3)-substituted isoquinuclidines was prepared from these decomplexed dihydropyridines.
273 cally transparent and stable organic glasses were prepared from these materials using a bulk melt-cas
275 ico and the United States in 2009, a vaccine was prepared from this virus to immunize the entire US p
276 d on a molecular water oxidation precatalyst was prepared from TiO2-protected n- or p(+)-Si coated wi
278 ibers with diameter of approximately 100 mum were prepared from triethylamine-quaternized-poly(vinylb
279 nates of human biofilm-positive colon mucosa were prepared from tumor patients (tumor and paired norm
280 functionalized tetrafluoroethylene fragment was prepared from two CF2 building blocks: ethyl bromodi
281 Marine phospholipids liposomal dispersions were prepared from two authentic standards (phosphatidyl
288 tin, nucleoplasmic and cytoplasmic fractions are prepared from UV-crosslinked cells and then subjecte
289 rous networks with tuneable pore sizes could be prepared from various materials, for example, NaBr, c
290 ealing that a dry and compactible powder can be prepared from various omega-3 oils and beta-cyclodext
291 this work, 1,2-disubstituted benzimidazoles were prepared from various mono- and disubstituted ortho
293 Co) and iron-nitrogen-doped carbon (C-N-Fe), was prepared from vitamin B12 (VB12) and the polyaniline
296 analysis of simulated clinical samples that were prepared from whole blood using a magnetic bead cap
299 cloaddition between both reactants which can be prepared from wood-based starting materials according
300 nd potential and allows better reductants to be prepared from Zn(1-x)Mg(x)O nanocrystals than can be