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1 intensification levels (average-yielding and high-yielding).
2 ating precursor under mild conditions and in high yield.
3 bstituted alpha-iodo-enamides in moderate to high yield.
4 Both steps proceed in very high yield.
5 atives and related polycycles in moderate to high yield.
6 idazoles or 1,4,6,9-tetramethoxyphenazine in high yield.
7 teral semiconductor-metal homojunctions with high yield.
8 talyzed Suzuki coupling with boronic acid in high yield.
9 ation of pure CD8(+) T cells at low cost and high yield.
10 hen couple to N-terminal proline residues in high yield.
11 synthesized by this single-step approach in high yield.
12 rmacologically interesting ring systems with high yield.
13 ynthesis of alkyl-substituted acylsilanes in high yield.
14 to give Boc-protected alpha-aminopyrroles in high yield.
15 and heterojunctions were also prepared with high-yield.
16 site-specific incorporation into proteins in high yields.
17 ees alcohols with a wide substrate scope and high yields.
18 cellular phospholipids have been obtained in high yields.
19 s a catalyst led to quinoline derivatives in high yields.
20 ides Se-arylated imidazolines in moderate to high yields.
21 litate carboxylation to give the products in high yields.
22 nder catalyst-free conditions in moderate to high yields.
23 can be synthesized using this method in very high yields.
24 mperature with a series of aryl chlorides in high yields.
25 (4-nitrophenyl)thio]-1-pyrrolines in good to high yields.
26 s, to form aryl alkyl and dialkyl ketones in high yields.
27 anhydrides to provide alpha-cyanoacetates in high yields.
28 provides highly substituted 2-oxazolines in high yields.
29 es and machines with nanometre precision and high yields.
30 c alcohols to aldehyde or ketone products in high yields.
31 is of dibenzo[a,c]acridines with moderate to high yields.
32 ibits a broad functional group tolerance and high yields.
33 he regioselective synthesis of oxazolines in high yields.
34 s, to provide access to cyclic aminodiols in high yields.
35 atures, in an open flask, and generally with high yields.
36 ion, the synthesis of biaryls in moderate-to-high yields.
37 es allows for chain-end functionalization in high yields.
38 quinazolin-11-one derivatives in moderate to high yields.
39 ,2-diketones to deliver amides and imides in high yields.
40 landscapes with high edge densities achieved high yields.
41 the ortho-substituted products in modest to high yields.
42 tmosphere to deliver the target molecules in high yields.
43 yclic molecules were prepared in moderate to high yields.
44 arious alkylated arene products with good to high yields.
45 ich the bridgehead nitrones were isolated in high yields.
46 ffords enantioenriched gamma-fluoroamines in high yields.
47 formed to carboxylates or ketones in good to high yields.
48 structure in generating singlet oxygen with high yields.
49 The reaction has shown to be general and high yielding.
50 Vacuum assisted infusion of GSP results in a high yield (~1 mg/g) of trans-Res and improved photostab
51 digital and analog CNT TFT circuits based on high-yield (19.9%) and ultrahigh purity (99.997%) polyme
52 iding the C2-allylated products in typically high yields (40-99 %) and enantioselectivities (83-99 %
56 r under short reaction times (<2 h), provide high yields (77-99%), and do not require column chromato
58 isolated in gram amounts (up to 5 g) and in high yields (80-96%) and characterized by NMR, ESI-HRMS,
59 ives have been synthesized from single step, high yielding (82-92%) chemistry involving a 4-hydroxyco
60 The peptide conjugations were carried out in high yield (90%) with their functional groups intact.
63 wave treatment paves the way to sustainable, high yield and cost-effective synthesis of GQDs for prac
66 boryl) substituent each were hydrogenated in high yield and enantioselectivity using C(1)-symmetric p
67 le alkyl-substituted alkynes and Bu(3)SnH in high yield and good regioselectivity; these products are
71 nched few-layered nanosheets are produced in high yield and in a reproducible and controlled manner.
73 ltetrazinyl functionality was synthesized in high yield and labeled endogenous MAGL in live cells.
74 rdiomyocytes can be generated routinely with high yield and purity for disease research and drug deve
78 ified SDS-LiCl method successfully extracted high yield and quality RNA from mature, developing, and
85 s three chiral centers have been prepared in high yield and stereocontrol from silyl-protected Z-gamm
86 teroaryl, vinyl, or cyclopropyl aldimines in high yield and with excellent diastereo- (up to >20:1) a
87 s containing indole-bearing stereocenters in high yield and with excellent levels of enantioinduction
89 e range of functional groups are obtained in high yield and with good regio-, diastereo-, and enantio
91 enophile reactive pairs proceeds rapidly, in high yield and with tunable stereochemical preferences o
94 ZEI 443 x ENT 13 and TZEI 462 x TZEI 10 were high yielding and stable; they out-performed the three e
96 ne substrates to their respective alkanes in high yields and diastereoselectivities and introduces a
98 mino acid derivatives were hydrogenated with high yields and enantioselectivities, affording chiral c
100 ged dinitrogen heterocycles were obtained in high yields and excellent diastereo- and enantioselectiv
101 iding attractive pyrrolo-azepine products in high yields and excellent enantioselectivities (99% ee).
103 rboxylation and loss of acetone, proceeds in high yields and excellent enantioselectivity (up to 99 %
106 The reaction proceeds at room temperature in high yields and is applicable to a broad range of substr
107 substrates leading to the final products in high yields and providing excellent stereocontrol in the
111 additive enables the preparation of KATs in high yields and with good functional group tolerance.
112 ohols, and homoallylic alcohols in modest to high yields and with moderate to excellent diastereosele
113 um of homoallylic diazoacetate substrates in high yields and with up to 99 % enantiomeric excess.
114 tic Grignard reagents at room temperature in high yields and within a few minutes' residence time, co
115 rovide the guidelines for the consistent and high-yield and high-quality hiPSC-CMs production in card
117 engineered EMs were nanosized, produced at a high yield, and displayed the anti-PSMA peptide, exosoma
118 he parent bridging amide produced ammonia in high yield, and treatment of the nitride with PhSH was f
120 ns in high enantiopurity (>99.9% de and ee), high yields, and on a preparative scale via benzofuran c
121 Industrial hemp (Cannabis sativa L.) is a high-yielding annual crop primarily grown for fiber, see
123 scribed acylimidazole reagents that react in high yields at 2'-OH groups stochastically at nonbase-pa
124 Hirao coupling occurred straightforwardly in high yields at positions 3, 5, and 6 of imidazopyridine
125 st positions around the two rings in good to high yields at synthetically relevant scales (1.5 g L(-1
126 study, we reciprocally crossed Horkuch with high yielding but salt sensitive IR29 to detect the comp
127 e (TPMA(3Cl) ) were replaced in one step and high yield by electron-donating cyclic amines (pyrrolidi
128 ocyclic building blocks, were synthesized in high yield by the reaction of sodium azide with 2H-aziri
129 mbal melanocytes, which could be expanded at high yield by using recombinant laminin (LN)-511-E8 as c
130 conjugated dyes were synthesized in good to high yields by a cascade of Pd-catalyzed Suzuki-Miyaura
131 tic potassium acyltrifluoroborates (KATs) in high yields by treating the in situ formed tetracoordina
133 ducts that can be obtained through one-step, high-yielding, catalytic transformations of the mono-, d
138 ficial selection on allocation has generated high-yielding crops that often invest the bare minimum i
140 y Arunachal rice landraces are comparable to high yielding cultivars with added advantage of signific
142 atalytic system that leads to unprecedented, high-yielding dearomative C-4 functionalization of quino
144 es of azaaryl ketones, esters, and amides in high yield, diastereoselectivity, and enantioselectivity
147 ification of biocatalysis as demonstrated in high yield esterifications and in the sesquiterpene cycl
149 tion proceeds at room temperature to provide high yields-even on multigram scales-of nitrogen heteroc
150 lex chiral secondary homoallylic alcohols in high yield, excellent diastereoselectivity, and usually
152 ent practices increased yield beyond that of high-yielding farmers by up to 7% in small plots (8 site
155 scale-up to deliver 2-alkyl-N-arylindoles in high yields followed with only a single purification ste
156 n derived from a benzylic nitrile proceed in high yields for a variety of peroxides, including those
157 a short time in inert solvents leads to the high-yield formation of benzo- and hetero-fused 1H-pyrro
158 P, FXR1P, and FXR2P from Escherichia coli in high yields, free of protein and nucleic acid contaminat
159 enzylidene/aminoalkylidene)indolin-2-ones in high yield from 2-oxindole and aryl/alkyl nitrile in the
160 loids, methylisatoid and cephalanthrin B, in high yields from simple precursors under mild and metal-
161 of an Ir(III) complex leads to efficient and high yielding fused gamma-lactam formation across a rang
162 tan-2-one-based tetracycles were obtained in high yield (generally >99%) and with excellent diastereo
163 assemble colloidal molecules (CMs); however, high-yield generation of patchy nanoparticles remains a
166 ose substituents have been introduced in one high-yielding glycosylation with an N-phenyl trifluoroac
167 recent technical renaissance has facilitated high-yielding (grams of protein per litre), cell-free ge
168 is observed that transition metal nucleated, high yield growth of carbon nanotubes (CNTs) is inhibite
169 standard fabrication tools and supports the high-yield growth of thousands of bicrystals per wafer,
170 prene polymerization, leading to polymers in high yields (>95%) and with high (>90%) cis-1,4-polyisop
174 ass-derived sugars into biofuel will require high yields, high volumetric productivities and high tit
176 At conditions relevant to mixing regions in high-yield implosions, we observe persistent chunks of c
177 cannabinoid CB(2) receptor was expressed at high yield in Expi293F mammalian cell cultures, solubili
178 ic, and cysteine-free and can be produced in high yields in a prokaryotic host, such as Escherichia c
182 li However, obtaining pure selenoproteins at high yields is limited by the accumulation of free Sec i
183 logy, the present study is a rare example of high-yield isolation and spectroscopic characterization
184 ation of NDI in these DNA hairpins generates high-yield, long-lived, entangled spin qubit pairs at 85
185 f the most important courgette diseases with high yield losses and is currently controlled by fungici
188 oxidation strategy to efficiently refold two high-yielding monomeric E2 species, D123 and a disulfide
192 m highly viscous CEW in a single step with a high yield of 94.3% and a purification factor of 15.7.
196 ty of an immortalized cell line to produce a high yield of exosomes with cross-species efficacy.
197 The GQDs are successfully synthesised with a high yield of over 84%, the highest value reported to da
198 ir low oxidation potentials, which lead to a high yield of photoluminescence-quenching hole trapping
199 n extended to benzylic substrates, providing high yield of the mono- and geminal bis-borylation produ
200 azole reagent is then carried out, providing high yields of 2'-OH conjugation at predetermined sites.
201 kinetic resolution by crystallization gives high yields of a N-(phenylsulfonyl)alkyloxazolidinone th
202 nduced pluripotent stem cells that generates high yields of an osteogenic cell-matrix (ihOCM) in vitr
206 ematopoietic stem cells (HSCs) can result in high yields of hematopoietic progenitor cells, this gene
207 ation reactions with these catalysts produce high yields of heteroarylsilanes from functionalization
210 reproducible synthesis, good solubility, and high yields of these clusters render them perfect starti
211 d catalytic activity for the degradation (in high yields) of New Fuchsine (NF), Methylene Blue (MB),
212 ow to select crop cultivars that can produce high yields on N-deficient soils has become crucially im
214 uropixels recordings can be carried out with high yields over multiple months in rats or other simila
215 cal studies, clinical trials have focused on high-yield pathophysiologic mechanisms, including protei
216 Saccharomyces cerevisiae and found that the high-yield pathway shows lower protein efficiency than t
217 -Aryloxy-naphthalimide 3 is an efficient and high-yielding photochemical precursor of dG(N(1)-H)(*) t
220 phipathic polymers offer a valuable tool for high-yield production of intact, detergent-free prions t
222 anti-EGFR fibronectin (FN3)-based PARs with high yield, rapid protein production, predicted low immu
231 tone isomers along stepwise, controlled, and high-yielding routes via porphyrin -> tetrahydroxyisobac
232 ters; and capacity building through low-tech high-yield screening are promising strategies for scale-
235 nal modification is particularly useful as a high-yielding, site-selective modification strategy that
236 Here we report the solution-phase and the high-yielding solid-phase syntheses of discrete oligoure
241 lay promising mechanical properties, such as high yield strength and uniform elongation, compared to
243 newable biomass resource is utilised for the high yield synthesis of GQDs via microwave treatment.
246 a semi-solid process featuring ultrafast and high-yield synthesis, and outstanding scalability for re
248 rotocol has been developed for the selective high-yielding synthesis of nearly fifty examples of prop
249 Interestingly, a practical, scalable, and high-yielding synthesis of pyridylphenol derivatives was
254 This animal work implicates potentially high-yield targets that may be leveraged in the future f
257 ide with PhSH was found to liberate NH(3) in high yield through a reaction that engages the redox-act
258 ved substitution of fluorine, which leads to high yields through rapid reactions under soft condition
259 ied to be the critical factor in maintaining high yield to the C(5+) ketones and the stability of the
260 e C(sp(2))-H activation in aqueous medium in high yields to demonstrate the practicability of this pr
261 from 2H-azirin-2-carbonyl chlorides, led in high yields to the formation of 2-(diazoacetyl)pyrroles,
264 esence of this competing capture DNA during 'high yield' transcription, leads to an increase in the y
265 ocompatibility, selectivity, and a rapid and high-yielding turnover for a wide variety of application
266 efficient release of homopiperonylic acid in high yield under simulated physiological conditions.
268 t hydrazones, which were prepared in good to high yields under smooth reaction conditions with very g
272 e alkynylation of trifluoromethyl ketones in high yield (up to 99 %) and high enantioselectivity (up
273 oxylic acids are isolated as sodium salts in high yields (up to 77%) by direct precipitation from the
274 an all-carbon quaternary, were prepared with high yields (up to 78%) and excellent stereoselectivity
275 mina converts various polyethylene grades in high yields (up to 80 weight percent) to low-molecular-w
277 groups and furnishes the desired products in high yields (up to 92%) with excellent stereoselectiviti
278 o furnish a wide range of propargylamines in high yields (up to 94%) and excellent enantioselectiviti
279 which yielded gamma-nitro aldehydes in very high yields (up to 95%), with high diastereoselectivity
280 lized indolines (18 examples) is obtained in high yields (up to 96%) under mild reaction conditions (
282 r downstream derivatisation were obtained in high yields (up to 99 %) and consistently high enantiose
284 d inclusion compound has been synthesized in high yields using an innovative and proficient acoustic
285 rmits the preparation of target compounds in high yields using readily available arylhydrazines and o
287 nediimide (AzaBPDI) dyes were synthesized in high yields via a new reaction sequence involving an imi
289 In addition to isolating butenolides in a high yield, we have also determined precisely when dimer
290 ded vinylidene boronic esters in moderate to high yields, while electron-deficient aromatic and vinyl
291 on functionality and proceeds in moderate-to-high yield with secondary amines, and moderate-to-low yi
293 d to achieve these bond forming processes in high yields with excellent stereocontrol, but few offer
294 stituted and functionalizable piperazines in high yields with excellent stereoselectivity (de, ee >99
295 protected alkyl, alkenyl and aryl amines in high yields with gaseous N(2) and CO(2) as the only bypr
298 stereogenic centers are obtained in good to high yield, with high enantioselectivity and diastereose
299 l disubstituted cyclobutyl boronic esters in high yields, with full stereospecificity and high levels