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1 d with the synthesis of a family of bicyclic fluorinated 1,3-amino alcohols.
2 omimetic building blocks containing backbone-fluorinated 1,4-disubstituted 1,2,3-triazole moieties.
3 parallel strand orientation incorporating 2'-fluorinated 2'-deoxyribonucleosides with canonical nucle
4 diated Yamamoto-type diaryl homocoupling of (fluorinated) 2,3-bis(4'-bromophenyl)quinoxaline precurso
5 y the addition of traces of partly insoluble fluorinated acrylate.
6 polymerization protocol is reported for semi-fluorinated acrylates and methacrylates.
7                                          Ten fluorinated AFFF concentrates, 9 of which were obtained
8                                      Whereas fluorinated alcohols are relatively abundant and tractab
9 oselectivity in glycosylations with a set of fluorinated alcohols as well as carbohydrate acceptors.
10 CC coupling of 1,1-disubstituted allenes and fluorinated alcohols to form homoallylic alcohols bearin
11 od represents a direct route to prepare beta-fluorinated aldehydes.
12 s (SiPcs, 1-7) with non-, partially- and per-fluorinated aliphatic (linear or branched at the alpha-c
13 ence of fluorination on the lipophilicity of fluorinated aliphatic alcohols was determined, and the l
14 h this reaction provides efficient access to fluorinated alkanes from a pool of starting materials th
15                                    Partially fluorinated alkanes, arenes, and alkenes can be transfor
16 and achieves the coupling of a wide range of fluorinated alkyl halides with alkylzinc reagents at roo
17                                Per- and poly fluorinated alkyl substances (PFASs), notably perfluoroo
18             A range of unnatural enantiopure fluorinated alpha-amino acids were obtained through sequ
19 5.1.0]octanes) based on a domino reaction of fluorinated alpha-bromoenones with beta-amino alcohols w
20 d to generate a versatile synthon for highly fluorinated alpha-phenyl acetic acid derivatives, which
21  with sterically unhindered monomers using a fluorinated aluminum salph complex with a substoichiomet
22 nt synthesis methods for the construction of fluorinated amines rely on air and moisture sensitive re
23                                      Flowing fluorinated amines through sequential reactor coils medi
24    With advances in cryoprobe production and fluorinated amino acid incorporation strategies, protein
25 g reaction at the C-terminal position of the fluorinated amino acid was conveniently performed under
26                                              Fluorinated amino acids serve as valuable biological pro
27 veloped that provides direct access to (18)F-fluorinated amino acids.
28                           The aforementioned fluorinated ammonium cations were isolated as room tempe
29 eatment of [LFe3(PhPz)3OFe][OTf]2 (1) or its fluorinated analog [LFe3(F2ArPz)3OFe][OTf]2 (5) with iod
30                            Inhibition by the fluorinated analog also suggests that the PMD utilizes a
31 of PIDA is comparable if not superior to its fluorinated analog phenyliodine(III) bis(trifluoroacetat
32  (1-F) were studied in comparison to its non-fluorinated analogue (1-H).
33 lso report the synthesis and reactivity of a fluorinated analogue and the structure of its covalently
34 od was applied for gram-scale synthesis of a fluorinated analogue of G protein-coupled receptor antag
35 ns (methyl to n-butyl) as well as some omega-fluorinated analogues (3-fluoropropyl and 4-fluorobutyl)
36 lysaccharide, LPS), we designed a library of fluorinated analogues aiming for an [(18)F]-labeled radi
37                              Four side chain fluorinated analogues of 1alpha,25-dihydroxy-19-norvitam
38            These compounds are precursors of fluorinated analogues of l-carbidopa, which is known to
39 application, the synthesis of a new class of fluorinated analogues of the neuroprotective tripeptide
40 reactions carried out in the presence of non-fluorinated analogues.
41 er, contains a combination of chiral-racemic fluorinated and achiral hydrogenated dendrons (RHF) in i
42 ms are explored by ab initio calculations of fluorinated and hydrogenated diamond (111) surfaces inte
43 cular balances were synthesized that contain fluorinated and nonfluorinated alkyl groups.
44           The contrasting preferences of the fluorinated and nonfluorinated ligands to generate prism
45  and diffusion of water vapor and CO2 in the fluorinated and nonfluorinated structures.
46  synthesis of chiral beta-hydroxylated, beta-fluorinated, and beta-arylated carboxylic acids.
47                   We report the synthesis of fluorinated anilines by palladium-catalyzed coupling of
48 tadentate ligand with strategically designed fluorinated arene groups in the second coordination sphe
49 en dictated by the innate electronics of the fluorinated arene, limiting the synthetic utility of the
50 otocatalytic C-F functionalization of highly fluorinated arenes is a powerful method for accessing fu
51 eviously, such as monofluorobenzenes and non-fluorinated arenes.
52 ity observed in the C(sp(2))-H borylation of fluorinated arenes.
53 enerated from nitroalkanes with a variety of fluorinated arenes.
54 inding protein) using commercially available fluorinated aromatic amino acids and fluorinated precurs
55 n/Prophenol-catalyzed Mannich reaction using fluorinated aromatic ketones as nucleophilic partners fo
56 C-H bond silylation is facile with partially fluorinated aromatic substrates containing two ortho flu
57 tution is predicted to be preferred for most fluorinated aromatics.
58 rans-metal-trapping (TMT) to a series of key fluorinated aromatics.
59 ur strategy resulted in materials containing fluorinated azobenzenes that retain their photochemical
60                 The PNA oligomers containing fluorinated bases form hybrids with cDNA/RNA with slight
61                                  A series of fluorinated benzenesulfonamides with substituents on the
62                    Enantiomerically enriched fluorinated benzo-fused bicyclic homoallylic amines have
63 non-covalent interactions between side-chain fluorinated benzyl esters and main-chain terminal arenes
64 fficient method for the preparation of ortho-fluorinated benzylamines.
65                A method for the synthesis of fluorinated beta'-amino beta-dicarbonyl compounds using
66                                              Fluorinated beta-diketonates NaRE(hfac)4 (RE = Y (1), Er
67  for the synthesis of a wide range of highly fluorinated biphenyls.
68 g that the same family of fully or partially fluorinated boron Lewis acids allows for the related H-H
69                                              Fluorinated boronic acid-appended benzyl bipyridinium sa
70  alternative strategy, we present the use of fluorinated boronic acid-appended pyridinium salts in co
71 fluorinated monosaccharides is achieved by a fluorinated building block approach.
72     Thus, the interaction of gold salts with fluorinated building blocks has been revised.
73 oute to the stereoselective synthesis of key fluorinated building blocks of high value for medicinal
74 ted by gold species meet species with either fluorinated building blocks or fluorinating reagents, ne
75 , thus enabling access to a diverse array of fluorinated building blocks.
76 ves, which provide straightforward access to fluorinated building blocks.
77 g 2'-fluoro substituents ((F)iCd, (F)iGd and fluorinated canonical 2'-deoxyribonucleosides) stabilize
78                                              Fluorinated carbohydrates are invaluable tools to study
79 hols was determined, and the log P values of fluorinated carbohydrates were measured.
80 e the pronounced polarity of C-F bonds, many fluorinated carbon compounds are hydrophobic: a controve
81                                              Fluorinated carboplatin ((19)F-FCP) was synthesized usin
82 e calculated transition states show that the fluorinated catalysts have stronger N-H...O and C-H...F
83                                The signal of fluorinated cells detected by a clinically applicable (1
84 e fluorine effect on the reactivity of alpha-fluorinated CH acids has remained largely unexplored.
85 decarboxylate the uPFCAs then focused on the fluorinated chains in the first MS quadrupole.
86    This strategy provided access to both new fluorinated chemical entities and nonfluorinated derivat
87 allowing for the generation of unprecedented fluorinated chemical entities.
88  for identification of previously unreported fluorinated chemicals in a timely and cost-efficient way
89                                        Chain-fluorinated cholesterol was used to measure cholesterol
90 xamples of asymmetric reactions that involve fluorinated components either as reactants, catalysts, s
91 es and polymerization thermodynamics of this fluorinated compound (1-F) were studied in comparison to
92         These compounds, as well as 25 other fluorinated compounds and metabolites, were analyzed in
93 d FTPs to allow degradation testing, and for fluorinated compounds at least as long as C12.
94 mulate TCE dechlorination, while some of the fluorinated compounds in certain AFFF formulations can i
95 trometry detector (LC-ESI-TOFMS) to identify fluorinated compounds in natural waters collected from l
96 e the occurrence and identity of replacement fluorinated compounds in surface water and sediment of t
97                      In contrast, only a few fluorinated compounds made by living organisms have been
98 ectfluor in acetone/water provides access to fluorinated compounds under mild and straightforward rea
99 inities, allowing for rapid screening of non-fluorinated compounds when a single fluorinated ligand f
100 ented, enabling the measurement of log P for fluorinated compounds with or without UV activity regard
101                   In asymmetric synthesis of fluorinated compounds, significant achievements are the
102  allow more facile access to a wide range of fluorinated compounds.
103      "Fluoro" refers to both fluorescent and fluorinated compounds.
104  of determining the sorption kinetics of any fluorinated contaminant, this work also highlights the s
105 yields (19)F T2 NMR relaxation values of any fluorinated contaminant, which are among the most danger
106 2,1,3-benzothiadiazole (DTBT) moiety and its fluorinated counterpart are important pi-conjugated buil
107 nus dendrimers contain either chiral-racemic fluorinated dendrons and a green fluorescent dye conjuga
108 tain environmentally friendly chiral-racemic fluorinated dendrons in their hydrophobic part (RF), one
109                                    While the fluorinated derivative, in the solid state, packs with a
110  a C-F bond driven Diels-Alder reaction of a fluorinated dienophile and a borole that shows remarkabl
111  isocyanate with fluorinated imines 1, while fluorinated dihydropyridin-2(1H)-ones 7 are prepared whe
112 ow that we can achieve the production of the fluorinated diketide 2-fluoro-3-hydroxybutyrate at appro
113                                         This fluorinated diketide can be used as a monomer in vivo to
114 ition of silylated nucleobases onto model C2-fluorinated dithioacetal substrates resulted in 1,2-syn
115                                   Two hybrid fluorinated double-chain surfactants with a diglucosylat
116  pharmaceuticals, and the number of approved fluorinated drugs is increasing each decade.
117 toolset for these materials utilizing highly fluorinated electrolytes based on a HFE solvent.
118 work we explore how an electrolyte additive (fluorinated ethylene carbonate - FEC) mediates the thick
119  in solid medium within glass capillaries or fluorinated ethylene propylene tubes.
120 e with fluoromalonyl-CoA allows insertion of fluorinated extender units at 43% of the yield of the wi
121 sease (COPD) by using free-breathing dynamic fluorinated (fluorine 19 [(19)F]) gas magnetic resonance
122 lic alphagammaalpha-tripeptides derived from fluorinated-furanoid sugar amino acid frameworks act as
123 onic structure calculations, we predict half-fluorinated GaBi honeycomb under tensile strain to harbo
124 e computed the electronic spectrum of a half-fluorinated GaBi nanoribbon with zigzag edges, which sho
125                       Cellular uptake of the fluorinated gamma-CF2-apg PNAs in NIH 3T3 and HeLa cells
126 n MR imaging during inhalation of a normoxic fluorinated gas mixture (perfluoropropane) and by using
127 sions of high-global-warming potential (GWP) fluorinated gases, the fastest growing sector of greenho
128                               Here we report fluorinated gold nanoparticles (f-AuNPs) designed to fac
129 nes, esters, nitriles, primary amides, alpha-fluorinated halo-acetates and perfluoroalkyl iodides.
130                                The uptake of fluorinated homooligomeric PNAs by HeLa cells was as fac
131         Here, we report the preparation of a fluorinated hydrocarbon two-dimensional polymer that can
132  molecules to this organelle, we synthesized fluorinated hydrophobic analogues of the fluorophore rho
133 al pathway controlled by the ER, we linked a fluorinated hydrophobic rhodol to 5-nitrofuran-2-acrylal
134                                              Fluorinated hydrophobic rhodols are outstanding fluoroph
135 ed by the reaction of phenyl isocyanate with fluorinated imines 1, while fluorinated dihydropyridin-2
136    A gold-catalyzed Povarov-type reaction of fluorinated imino esters and furans is described.
137 n conjunction with our previous work on PNAs fluorinated in backbone and at N-terminus, it is evident
138                                          The fluorinated indazole group offers a handle for further f
139 al-free method for accessing a wide range of fluorinated indoles is described.
140 oil at AFFF-impacted sites and suggests that fluorinated intermediates that are not routinely measure
141                                  A series of fluorinated Ir(III)-terpyridine-phenylpyridine-X (X = an
142                       As proof of concept, a fluorinated isoquinoline alkaloid, (18) F-aspergillitine
143                                        Eight fluorinated isosteric alpha-d-glucopyranosyl 1-phosphate
144  phosphorylated, hydroxylated), and labeled (fluorinated, isotopically labeled) side chains to be add
145 ullerene organic solar cells (OSCs) based on fluorinated ITIC-Th1 electron acceptor and a wide-bandga
146                Indeed, the results show that fluorinated ITIC-Th1 exhibits redshifted absorption, sma
147                               A new class of fluorinated lactones was prepared by the intramolecular
148 g of non-fluorinated compounds when a single fluorinated ligand for the binding pocket of interest is
149  perfluoropolyether (PFPE), formulated these fluorinated ligands as aqueous nanoemulsions, and then m
150     This work demonstrates the usefulness of fluorinated ligands in designing molecule-selective and
151                                          The fluorinated ligands that are formed are retained at the
152   Therefore, (18)F-GE-180 is a promising new fluorinated longer-half-life tracer that reveals the pre
153                          After infusing with fluorinated lubricants, the fluorogels showed excellent
154  copolymers, providing facile access to semi-fluorinated macromolecules using a single methodology wi
155 ssing, fabrication, and functionalization of fluorinated materials with easy removal of the volatile
156 y for the fabrication of a chemically stable fluorinated metal-organic framework (MOF) material (NbOF
157 rate construction of a hydrolytically stable fluorinated metal-organic framework (MOF), NbOFFIVE-1-Ni
158                               Two mesoporous fluorinated metal-organic frameworks (MOFs) were synthes
159                       The incorporation of a fluorinated Mo(II)2 paddlewheel, B, into analogous Zn(II
160 e area of 2445 m(2) g(-1), the highest among fluorinated MOFs.
161 cations of these model systems to form small fluorinated molecules as well as fluoropolymers.
162 ein, we report the synthesis of a library of fluorinated molecules that contain nonafluoro-tert-butyl
163  Various applications could benefit from new fluorinated molecules that offer chemical handles for qu
164  We have been investigating the mechanism of fluorinated monomer insertion by three of the six differ
165 icient chain elongation after insertion of a fluorinated monomer.
166  control of the polymerization of main chain fluorinated monomers as exemplified by vinylidene fluori
167 TREN (TREN = tris(2-aminoethyl amine)), semi-fluorinated monomers with side chains containing between
168 lymerization of hydrophobic, hydrophilic and fluorinated monomers.
169 ionine S-adenosyl transferase-2 (MAT2A) with fluorinated N,N-dialkylaminostilbenes (FIDAS agents) off
170 d indole derivatives incorporating partially fluorinated n-propyl and n-butyl groups is described alo
171                                              Fluorinated n-type conjugated polymers are used as effic
172 s of blend films are improved by using these fluorinated n-type polymers to result in enhanced photoc
173 de novo designed peptide at the interface of fluorinated nanodroplets.
174  but our ability to produce site-selectively fluorinated natural products remains limited by challeng
175      Therefore, new approaches for accessing fluorinated nitrogen heterocycles are of great significa
176                 Maximal IH through beryllium-fluorinated NKA indicates that this complex mimics ATP-b
177                                        A new fluorinated nonfullerene acceptor, ITIC-Th1, has been de
178 pare the duplex stabilizing properties of 2'-fluorinated nucleic acid analogues with furanose and non
179    Our studies support further evaluation of fluorinated nucleic acid analogues with non-furanose sug
180  organoruthenium(II) chlorido complexes with fluorinated O,O-ligands [(eta(6)-p-cymene)Ru(F3C-acac-Ar
181 minium ions were successfully generated from fluorinated O-acetyl-N,O-acetal l-tartaric acid derivati
182 aqueous droplets surrounded by an immiscible fluorinated oil phase.
183                                        While fluorinated oligonucleotides form moderately stable para
184 orption properties often exhibited by highly fluorinated organic compounds, that is molecules rich in
185 ic asymmetric synthesis of other families of fluorinated organic compounds.
186                                              Fluorinated organic molecules are of interest in fields
187                                              Fluorinated organic molecules are playing an increased r
188          The activation of second-generation fluorinated oxazaborolidines by the strong acid triflimi
189     The utility of Tf2NH-TiCl4 activation of fluorinated oxazaborolidines is documented by examples i
190 ale starting from a readily available chiral fluorinated oxazolidine (Fox).
191 ional functionalities and the formation of 3-fluorinated oxindoles exhibiting an array of four adjace
192 lls from 2.93% (nonfluorinated P1) to 7.13% (fluorinated P2).
193 sing Selectfluor to afford the corresponding fluorinated paraconic esters in good yields as a single
194          In this context, we have designed a fluorinated PET radiotracer, [(18)F]2FNQ1P, that possess
195                                              Fluorinated pH indicators were produced with radiochemic
196 rhelical separation of the BM2 channel using fluorinated Phe-5.
197                           The combination of fluorinated phenylpyridine ligands with an electron-rich
198  route into valuable, densely functionalized fluorinated phosphonates that takes advantage of (i) a C
199               This work describes the use of fluorinated Pickering emulsions with nonadsorbing interf
200 d was demonstrated on both unfluorinated and fluorinated plastics, demonstrating high tracer recoveri
201 , we herein report the chemical synthesis of fluorinated PNA monomers and biophysical studies of deri
202 rse phase HPLC show higher hydrophobicity of fluorinated PNA oligomers, dependent on the number and s
203 ne and at N-terminus, it is evident that the fluorinated PNAs have potential to emerge as a new class
204                                 The backbone fluorinated PNAs, which are first in this class, when co
205          The preparation of high-performance fluorinated poly(aryl thioethers) has received little at
206 the authors show a highly efficient route to fluorinated poly(aryl thioethers) via an organocatalyzed
207 erein, we report a highly efficient route to fluorinated poly(aryl thioethers) via an organocatalyzed
208 remarkable reactivity enable rapid access to fluorinated poly(aryl thioethers), but also opens new av
209 of the volatile catalyst and TMSF byproducts.Fluorinated poly(aryl thioethers), unlike their poly(ary
210  can be used as a monomer in vivo to produce fluorinated poly(hydroxyalkanoate) (PHA) bioplastics wit
211 ated by laser-desorption of the near-planar, fluorinated polycyclic aromatic hydrocarbon (PAH), C60H2
212     A modular synthesis of regiospecifically fluorinated polycyclic aromatic hydrocarbons (PAHs) is d
213 assembling giant surfactants consisting of a fluorinated polyhedral oligomeric silsesquioxane (FPOSS)
214 -b-PEO) diblock copolymer tail tethered to a fluorinated polyhedral oligomeric silsesquioxane (FPOSS)
215                             By utilizing the fluorinated polymer (PBDB-TF) as the electron donor, the
216 hat, among others, degradation of side-chain fluorinated polymers in the environment and landfills ca
217 eir properties to those of the analogous non-fluorinated polymers shows that backbone fluorination le
218  polymers (FTACPs) are a class of side-chain fluorinated polymers used for a variety of commercial ap
219 d to increase by up to a factor of 5 for the fluorinated polymers.
220 n of these molecules, leading to a series of fluorinated polysubstituted imidazoles in gram scale.
221 ailable fluorinated aromatic amino acids and fluorinated precursors as example applications of the me
222      Intramolecular response was measured in fluorinated probes and intermolecular quenching by mixin
223 E)-1,1,3,4-tetrafluorobutadiene as the major fluorinated product.
224 nces in the isomeric ratio and the yields of fluorinated products obtained from N,N-disubstituted-phe
225                            The silylated and fluorinated products were obtained as single isomers in
226 building blocks for the synthesis of various fluorinated products.
227 g multiple chain extensions to form multiply fluorinated products.
228                                      Over 73 fluorinated proteins have been studied by (19)F NMR sinc
229 portant substituted spirooxindole as well as fluorinated pyran scaffolds.
230 uous flow synthesis of highly functionalized fluorinated pyrazoles and pyrazolines has been developed
231                          Chemotherapy with a fluorinated pyrimidine and a platinum agent, followed by
232                    The crystal structures of fluorinated racemic PNA monomers reveal interesting base
233 H, CH2F, and CH2CF3, are used as a source of fluorinated radicals to add fluoroalkyl groups to electr
234                     This work has focused on fluorinated radiotracers, which would enable wider use a
235 ylacetates, the synthetic equivalence of the fluorinated reagent with alpha-nitro-alpha-diazo carbony
236                          We report a pair of fluorinated, redox-active copper complexes for potential
237 er a competitive equilibrium with a selected fluorinated reporter ligand, the dissociation constant (
238 brid DSs mediated by the hybrid hydrogenated-fluorinated RHF Janus dendrimer.
239 e a strong focus on the development of novel fluorinated RNA derivatives that are powerful in NMR spe
240                  The kidney retention of the fluorinated sdAb was 20-fold lower than a (99m)Tc-labele
241 in, a series of 6-halopurines decorated with fluorinated side chains have been synthesized and evalua
242 his, two cholesterol analogs with truncated, fluorinated side chains have been synthesized and shown
243                                        A new fluorinated silicon reagent bearing a functionalized tet
244 ne illustrates the potential ease with which fluorinated small molecules relevant to neuroscience dru
245 g the potential to generate a broad range of fluorinated small-molecule targets in living cells.
246 of the HFC solvent in tandem with the highly fluorinated, solubilizing, weakly coordinating [Al(OR(f)
247 y simply modulating the starting peptide and fluorinated solvent concentrations during synthesis.
248                            The presence of a fluorinated solvent is essential for the success of thes
249 e to its greater oxidizing abilities in this fluorinated solvent such that in HFIP the reactivity of
250 o repel extremely-low-energy liquids such as fluorinated solvents, which completely wet even the most
251 omniphobic surface that can super-repel even fluorinated solvents, which highly wet all materials.
252 (19)F long-lived states in suitably designed fluorinated spy molecules allows one to perform competit
253                                        Using fluorinated starting materials, after mesylation, allowe
254        In this work, we made use of a highly fluorinated stationary phase and a series of benzene der
255 s is observed and calculated for planar ring-fluorinated stilbenes, trans-2,3,5,6,2',3',5',6'-octoflu
256 ishing between graphene, C2F chair and fully fluorinated stoichiometric CF 2D phases.
257  This work presents the synthesis of various fluorinated structural analogues of FTY720, their in vit
258 tely new reactivities and thus also to novel fluorinated structural scaffolds.
259 yl)pyrrolidin-2-one derivatives, bearing the fluorinated substituent on a tetrasubstituted carbon.
260  presence of the highly electron-withdrawing fluorinated substituent, cyclic alpha-trifluoromethylate
261 d herein, several alternative substrates and fluorinated substrate analogs were prepared to investiga
262                                         Less fluorinated substrates react slower.
263 describe the field of reactions of partially fluorinated substrates with transition metal atoms, ions
264 ity of the Povarov reaction to unprecedented fluorinated substrates, generating scaffolds that contai
265 e of substrates to give medicinally relevant fluorinated substructures with complete regiocontrol.
266 al analysis suggested a strong preference of fluorinated sugar rings for either a 2'-endo, 3'-exo (So
267 radical fluoroalkylation of isocyanides with fluorinated sulfones is enabled by visible-light photore
268 nly describes a new synthetic application of fluorinated sulfones, but also provides a new route to f
269 eview, we present the specific properties of fluorinated sulfoximines (including important bioactivit
270    This work demonstrated the utilization of fluorinated sulfur ylides as versatile reagents for Core
271                                 The obtained fluorinated sultones are attractive as potential electro
272 eal that "polar hydrophobicity" of the fully fluorinated surfaces is caused by a negligible surface/w
273 sites in Ontario, Canada, and two commercial fluorinated surfactant concentrates were characterized i
274  spectrometry assigned molecular formulas to fluorinated surfactant ions, while collision induced dis
275                                              Fluorinated surfactant-based aqueous film-forming foams
276 ge solid phase extraction (SPE) fractionated fluorinated surfactants based on ionic character.
277 ge number of novel and infrequently reported fluorinated surfactants in different AFFF formulations.
278 e interfacial tensions using hydrocarbon and fluorinated surfactants including stimuli-responsive and
279  investigated whether commercially available fluorinated surfactants, such as Scotchgard fabric prote
280 ere characterized in order to identify novel fluorinated surfactants.
281  we show that lower charge separation in the fluorinated system is associated with the formation of b
282 weakened solid-fluid binding energies in the fluorinated systems.
283                                      The two fluorinated tc-nucleosides were also incorporated into a
284 ane at room temperature, gives rise to novel fluorinated tetrahydrofuran-fused tetrahydroquinolines i
285                                   Several 2'-fluorinated tetrahydrouridine derivatives were synthesiz
286 ction of beta-fluoroamine motifs featuring a fluorinated tetrasubstituted carbon.
287 erminal end of the alkyl group is completely fluorinated, the balance tips toward fluorophobicity and
288 inding opens perspectives in the delivery of fluorinated therapeutic molecules and biomarkers.
289  a wide bandgap polymer donor PM6 containing fluorinated thienyl benzodithiophene (BDT-2F) unit and a
290                     The synthesis of the two fluorinated tricyclic nucleosides 6'-F-tc-T and 6'-F-tc-
291  The antiparallel self-assembled pore of the fluorinated tripeptides illustrates the selective ion-tr
292                                              Fluorinated tripodal compounds were recently reported to
293 metric properties of urea and thiourea-based fluorinated tripodal receptors are explored here for the
294 observed in the X-ray crystal structure of a fluorinated triterpenoid.
295 rks (MOFs) were synthesized from extensively fluorinated tritopic carboxylate- and tetrazolate-based
296     Supporting this model, substitution with fluorinated Trp analogues, with increased H-bonding prop
297  properties of tungsten adsorbed tri-vacancy fluorinated (TVF) graphene.
298                                              Fluorinated tyrosines (FnY's, n = 2 and 3) have been sit
299 this protocol, we quantified the amount of a fluorinated xenobiotic (heptafluorobutyric acid, HFBA) i
300                                 Furthermore, fluorinated ynamides, a new type of building block, were

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