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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  a minor impact on the atmospheric burden of fluorinated acids.
4 polymerization protocol is reported for semi-fluorinated acrylates and methacrylates.
5 ta(5) -C5 Me5 )(dppe)] with an electrophilic fluorinating agent (NFSI) results in the formation of th
6 artin periodinane oxidation reagent, and the fluorinating agent AlkylFluor.
7 te, which in the presence of Fe(3+) ions and fluorinated alcohol decomposes into ketone.
8                         Reactions proceed in fluorinated alcohol solvents at elevated temperatures an
9                                              Fluorinated alcohols as solvents strongly influence and
10 oselectivity in glycosylations with a set of fluorinated alcohols as well as carbohydrate acceptors.
11 s (SiPcs, 1-7) with non-, partially- and per-fluorinated aliphatic (linear or branched at the alpha-c
12 ence of fluorination on the lipophilicity of fluorinated aliphatic alcohols was determined, and the l
13                                    Partially fluorinated alkanes, arenes, and alkenes can be transfor
14 r for catalysts bearing one triflate and one fluorinated alkoxide than for catalysts bearing two trif
15 ide, with special properties imparted by the fluorinated alkyl chain.
16                                              Fluorinated alkyl groups are important motifs in bioacti
17 reaction is successful with a range of alpha-fluorinated alkyl sodium sulfinate salts and diarylphosp
18                                Per- and poly fluorinated alkyl substances (PFASs), notably perfluoroo
19 5.1.0]octanes) based on a domino reaction of fluorinated alpha-bromoenones with beta-amino alcohols w
20                            New, still highly fluorinated alternatives are produced in hopes of reduci
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                  LAT1 uptake was tolerant of fluorinated amino acid stereochemistry and chain length.
25 y non-natural derivatives, as shown here for fluorinated amino acid variants.
26 g reaction at the C-terminal position of the fluorinated amino acid was conveniently performed under
27                                              Fluorinated amino acids serve as valuable biological pro
28 arting materials in the preparation of novel fluorinated amino acids, anilines, and aliphatic amines
29 AT-mediated cancer cell uptake in a panel of fluorinated amino acids.
30 veloped that provides direct access to (18)F-fluorinated amino acids.
31 eatment of [LFe3(PhPz)3OFe][OTf]2 (1) or its fluorinated analog [LFe3(F2ArPz)3OFe][OTf]2 (5) with iod
32 ilable by this method serve as precursors to fluorinated analogs of sugars, amino acids, and other va
33  active compounds, and their enantioenriched fluorinated analogs should be of great interest in the s
34 2) /H(2) mixture, in comparison with the non-fluorinated analogue (43 h(-1) ) and a Au/TiO(2) heterog
35 lso report the synthesis and reactivity of a fluorinated analogue and the structure of its covalently
36 od was applied for gram-scale synthesis of a fluorinated analogue of G protein-coupled receptor antag
37 tituted azobenzene core and its tetra- ortho-fluorinated analogue, we have developed a set of uni- an
38 lysaccharide, LPS), we designed a library of fluorinated analogues aiming for an [(18)F]-labeled radi
39  and trifluoromethylisoxazoles, for example, fluorinated analogues of ABT-418 and ESI-09.
40 eaction has been applied to the synthesis of fluorinated analogues of diltiazem and tiazesim, both th
41            These compounds are precursors of fluorinated analogues of l-carbidopa, which is known to
42 application, the synthesis of a new class of fluorinated analogues of the neuroprotective tripeptide
43 port a new elemental ionization method where fluorinated analytes are introduced into an ICP to produ
44 ms are explored by ab initio calculations of fluorinated and hydrogenated diamond (111) surfaces inte
45 ted backbones, which incorporate hydrophobic fluorinated and hydrophilic sulfonic acid functional gro
46            This study aimed to determine the fluorinated and nonfluorinated chemical composition of a
47           The contrasting preferences of the fluorinated and nonfluorinated ligands to generate prism
48 rination approach enables the development of fluorinated and radiofluorinated compounds that can be d
49 is, heteroaryl-substituted acetaldehydes are fluorinated and then directly engaged in enantioselectiv
50  synthesis of chiral beta-hydroxylated, beta-fluorinated, and beta-arylated carboxylic acids.
51 m ions, 2) hexafluorophosphate salts, and 3) fluorinated antimony- and arsenic- compounds.
52 blished C(sp(2))-H oxidative addition of the fluorinated arene as the selectivity-determining step of
53 en dictated by the innate electronics of the fluorinated arene, limiting the synthetic utility of the
54 otocatalytic C-F functionalization of highly fluorinated arenes is a powerful method for accessing fu
55    The mechanism of C(sp(2))-H borylation of fluorinated arenes with B(2)Pin(2) (Pin = pinacolato) ca
56 )benzene, as well as a C-F bond in partially fluorinated arenes, to furnish borylation products under
57 ity observed in the C(sp(2))-H borylation of fluorinated arenes.
58 enerated from nitroalkanes with a variety of fluorinated arenes.
59 eviously, such as monofluorobenzenes and non-fluorinated arenes.
60 inding protein) using commercially available fluorinated aromatic amino acids and fluorinated precurs
61 n/Prophenol-catalyzed Mannich reaction using fluorinated aromatic ketones as nucleophilic partners fo
62 C-H bond silylation is facile with partially fluorinated aromatic substrates containing two ortho flu
63 rans-metal-trapping (TMT) to a series of key fluorinated aromatics.
64 rst racemization-stable helicene derivatives fluorinated at terminal rings, 1,2,3,4-tetrafluoro[6]hel
65 ion is realized in an LCE composed with an o-fluorinated azobenzene (oF-azo) monomer.
66 LCE to analogs prepared from classical and m-fluorinated azobenzene derivatives, the origin of the pe
67 e findings demonstrate that incorporation of fluorinated azobenzenes not just may alter photophysical
68                    Enantiomerically enriched fluorinated benzo-fused bicyclic homoallylic amines have
69 non-covalent interactions between side-chain fluorinated benzyl esters and main-chain terminal arenes
70                                              Fluorinated beta-diketonates NaRE(hfac)4 (RE = Y (1), Er
71  for the synthesis of a wide range of highly fluorinated biphenyls.
72  alternative strategy, we present the use of fluorinated boronic acid-appended pyridinium salts in co
73 cal fluorination, we prepared a series of 11 fluorinated branched-chain amino acids and evaluated the
74 fluorinated monosaccharides is achieved by a fluorinated building block approach.
75 oute to the stereoselective synthesis of key fluorinated building blocks of high value for medicinal
76 ted by gold species meet species with either fluorinated building blocks or fluorinating reagents, ne
77  alternative biosynthetic strategies towards fluorinated building-blocks.
78                                              Fluorinated carbohydrates are invaluable tools to study
79 hols was determined, and the log P values of fluorinated carbohydrates were measured.
80                                              Fluorinated carboplatin ((19)F-FCP) was synthesized usin
81 e calculated transition states show that the fluorinated catalysts have stronger N-H...O and C-H...F
82                                The signal of fluorinated cells detected by a clinically applicable (1
83 e fluorine effect on the reactivity of alpha-fluorinated CH acids has remained largely unexplored.
84 th a C(12)-hydrogenated chain and a C(4)F(9)-fluorinated chain emerged as the most potent additive ex
85 sts of a hydrogenated chain, and a partially fluorinated chain made of a propyl hydrogenated spacer t
86 allowing for the generation of unprecedented fluorinated chemical entities.
87 ous and crystalline forms of DFDT and a mono-fluorinated chiral congener, MFDT.
88 atalytic enantioselective synthesis of alpha-fluorinated chiral tertiary alcohols from (hetero)aryl m
89                                        Chain-fluorinated cholesterol was used to measure cholesterol
90 oring Na(2)F(+), resulting in detection of a fluorinated compound on a clothing item.
91 when lactate was the electron donor, and the fluorinated compound was the sole electron acceptor.
92         These compounds, as well as 25 other fluorinated compounds and metabolites, were analyzed in
93 he need for nontargeted detection of unknown fluorinated compounds and transformation products.
94 mulate TCE dechlorination, while some of the fluorinated compounds in certain AFFF formulations can i
95 measurements due to the rising importance of fluorinated compounds in pharmaceutical, environmental,
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 c-pressure elemental ionization method where fluorinated compounds separated by gas chromatography (G
99 ented, enabling the measurement of log P for fluorinated compounds with or without UV activity regard
100 n provide refinement of such models with the fluorinated compounds, which allows the explanation of t
101  as altered, shorter-chain PFAS and volatile fluorinated compounds, which were scrubbed effectively w
102                                        Fifty fluorinated compounds, with 28 novel experimental alipha
103 ors and has influenced the metabolic fate of fluorinated compounds.
104 well as the one-pot diversified synthesis of fluorinated compounds.
105  of determining the sorption kinetics of any fluorinated contaminant, this work also highlights the s
106 yields (19)F T2 NMR relaxation values of any fluorinated contaminant, which are among the most danger
107                                   Four novel fluorinated cyclic analogues of biphalin with excellent
108 arboxylate substrates, highly functionalized fluorinated cyclobutenes were obtained in excellent yiel
109 les, zinc phthalocyanine and its eight-times fluorinated derivative, with tunable energy levels based
110 ography (PET) radioligand [(11)C]RSR-056, 38 fluorinated derivatives were synthesized and tested by i
111 eparable mixture (1:1) of the PODs and their fluorinated derivatives.
112  a C-F bond driven Diels-Alder reaction of a fluorinated dienophile and a borole that shows remarkabl
113 ow that we can achieve the production of the fluorinated diketide 2-fluoro-3-hydroxybutyrate at appro
114                                         This fluorinated diketide can be used as a monomer in vivo to
115 ition of silylated nucleobases onto model C2-fluorinated dithioacetal substrates resulted in 1,2-syn
116                                   Two hybrid fluorinated double-chain surfactants with a diglucosylat
117  successfully applied them to characterize a fluorinated drug molecule, aprepitant, and its commercia
118 sitive spin for probing molecular details of fluorinated drug substances in solid formulations, due t
119 toolset for these materials utilizing highly fluorinated electrolytes based on a HFE solvent.
120 ither artificially preformed or derived from fluorinated electrolytes, and thus, the effect of the Li
121  high-concentration electrolytes, and highly fluorinated electrolytes, surface coatings that can form
122 oping, core-shell hollow host structure, and fluorinated ether electrolytes enables ultrastable Li st
123   In this work, we synthesize a new class of fluorinated ether electrolytes that combine the oxidativ
124 work we explore how an electrolyte additive (fluorinated ethylene carbonate - FEC) mediates the thick
125 e with fluoromalonyl-CoA allows insertion of fluorinated extender units at 43% of the yield of the wi
126 sease (COPD) by using free-breathing dynamic fluorinated (fluorine 19 [(19)F]) gas magnetic resonance
127 lic alphagammaalpha-tripeptides derived from fluorinated-furanoid sugar amino acid frameworks act as
128 onic structure calculations, we predict half-fluorinated GaBi honeycomb under tensile strain to harbo
129 e computed the electronic spectrum of a half-fluorinated GaBi nanoribbon with zigzag edges, which sho
130 n MR imaging during inhalation of a normoxic fluorinated gas mixture (perfluoropropane) and by using
131                  The environmental impact of fluorinated gases (F-gases) necessitates the development
132 rs took potentially confounding medications (fluorinated glucocorticoids and/or intravenous immunoglo
133                           Using a library of fluorinated glucose (Glc), mannose (Man), and galactose
134                                              Fluorinated glycosides are known to resist the glycosida
135 mes of either hydrogenated graphene (HG) and fluorinated graphene (FG).
136 on to more economically friendly small-chain fluorinated groups is leading to a resurgence in the syn
137 nes, esters, nitriles, primary amides, alpha-fluorinated halo-acetates and perfluoroalkyl iodides.
138          The changed electronic structure in fluorinated helicenes was reflected in a slight shift of
139 lar chains in the crystal structures of both fluorinated helicenes.
140                                       Select fluorinated heterocycles can be functionalized using thi
141                                The uptake of fluorinated homooligomeric PNAs by HeLa cells was as fac
142                                              Fluorinated hydrocarbon (FHC) contamination has attracte
143 bust bonds; consequently, the degradation of fluorinated hydrocarbons is exceptionally difficult.
144 ncapsulates (89)Zr in the fluorous oil via a fluorinated hydroxamic acid chelate.
145 n conjunction with our previous work on PNAs fluorinated in backbone and at N-terminus, it is evident
146                                          The fluorinated indazole group offers a handle for further f
147                                              Fluorinated ionic liquids (FIL/ILs) emerged as an altern
148                                  A series of fluorinated Ir(III)-terpyridine-phenylpyridine-X (X = an
149 e and pyrazole was shown by the synthesis of fluorinated Isocarboxazid and Mepiprazole analogues.
150                       As proof of concept, a fluorinated isoquinoline alkaloid, (18) F-aspergillitine
151                                        Eight fluorinated isosteric alpha-d-glucopyranosyl 1-phosphate
152  phosphorylated, hydroxylated), and labeled (fluorinated, isotopically labeled) side chains to be add
153 ullerene organic solar cells (OSCs) based on fluorinated ITIC-Th1 electron acceptor and a wide-bandga
154                Indeed, the results show that fluorinated ITIC-Th1 exhibits redshifted absorption, sma
155  perfluoropolyether (PFPE), formulated these fluorinated ligands as aqueous nanoemulsions, and then m
156     This work demonstrates the usefulness of fluorinated ligands in designing molecule-selective and
157 ce four fluorine atoms from OFCP to generate fluorinated macrobicyclic compounds that display dual-tu
158  copolymers, providing facile access to semi-fluorinated macromolecules using a single methodology wi
159 ssing, fabrication, and functionalization of fluorinated materials with easy removal of the volatile
160 hase (SEI) through the lithiation of surface-fluorinated mesocarbon microbeads (MCMB-F) anodes.
161 y for the fabrication of a chemically stable fluorinated metal-organic framework (MOF) material (NbOF
162 rate construction of a hydrolytically stable fluorinated metal-organic framework (MOF), NbOFFIVE-1-Ni
163       Thus, the hydration shell structure of fluorinated methyl groups results from a delicate balanc
164 current work ortho-fluorinated (OF) and meta-fluorinated (MF) analogs of (18)F-para-fluorinated (PF)-
165 ayer and intralayer space of two-dimensional fluorinated MOFs for capturing acetylene from ethylene.
166                          In turn, studies of fluorinated molecules are providing deeper insights into
167    Comparison of different monolayer-forming fluorinated molecules reveals important differences in r
168  Various applications could benefit from new fluorinated molecules that offer chemical handles for qu
169 literature associated with the metabolism of fluorinated molecules, focusing on examples where the pr
170  We have been investigating the mechanism of fluorinated monomer insertion by three of the six differ
171 icient chain elongation after insertion of a fluorinated monomer.
172  control of the polymerization of main chain fluorinated monomers as exemplified by vinylidene fluori
173 TREN (TREN = tris(2-aminoethyl amine)), semi-fluorinated monomers with side chains containing between
174 lymerization of hydrophobic, hydrophilic and fluorinated monomers.
175 roof-of-principle level with a library of 13 fluorinated monosaccharides to a set of three carbohydra
176 d potentially problematic outcomes with some fluorinated motifs and are enhancing our understanding o
177 thodologies that are providing access to new fluorinated motifs.
178 de novo designed peptide at the interface of fluorinated nanodroplets.
179 NT mimic structures via the self-assembly of fluorinated nanohoops, which can be synthesized in a sca
180                                        A new fluorinated nonfullerene acceptor, ITIC-Th1, has been de
181  report the identification of two subsets of fluorinated nonxanthine A(2B) adenosine receptor antagon
182 minium ions were successfully generated from fluorinated O-acetyl-N,O-acetal l-tartaric acid derivati
183 ), we investigated in the current work ortho-fluorinated (OF) and meta-fluorinated (MF) analogs of (1
184 nents that uses a mobile liquid interface (a fluorinated oil) to reduce the adhesive forces between t
185 The development of new fluids has focused on fluorinated olefins, known as hydrofluoroolefins (HFOs),
186  glycosyl donors is critical for assembly of fluorinated oligosaccharides.
187 afer and shows higher thromboresistance than fluorinated, omniphobic catheter surfaces, produced by p
188  and highly efficient OPV devices using both-fluorinated or both-nonfluorinated donor/acceptor blends
189 ite the growing interest in the synthesis of fluorinated organic compounds, few reactions are able to
190                                    In an all-fluorinated organic lean electrolyte, the C/S cathode ex
191                                              Fluorinated organic molecules are pervasive within the p
192                                              Fluorinated organic molecules are playing an increased r
193  Given the wide use and emerging concerns of fluorinated organics (e.g., per- and polyfluoroalkyl sub
194                                              Fluorinated organophosphorus(V) compounds are a very ver
195          The activation of second-generation fluorinated oxazaborolidines by the strong acid triflimi
196     The utility of Tf2NH-TiCl4 activation of fluorinated oxazaborolidines is documented by examples i
197 ional functionalities and the formation of 3-fluorinated oxindoles exhibiting an array of four adjace
198         In addition, the photolysis of a non fluorinated pentanone (2-methyl-3-pentanone, 2M3P) was s
199  meta-fluorinated (MF) analogs of (18)F-para-fluorinated (PF)-NB1, a 3-benzazepine-based radiofluorin
200  AFFF primarily containing electrochemically fluorinated PFASs for 10 days, followed by a 6 day depur
201 rhelical separation of the BM2 channel using fluorinated Phe-5.
202 oxy groups as bioisosteric replacements of a fluorinated phenyl ring and properties such as lipophili
203                     As an example, partially fluorinated Phos-POPs (F-Phos-POPs) were obtained with a
204  soft hydrogel as a conductor and an elastic fluorinated photoresist as the passivation insulation la
205 d was demonstrated on both unfluorinated and fluorinated plastics, demonstrating high tracer recoveri
206 rse phase HPLC show higher hydrophobicity of fluorinated PNA oligomers, dependent on the number and s
207 ne and at N-terminus, it is evident that the fluorinated PNAs have potential to emerge as a new class
208          The preparation of high-performance fluorinated poly(aryl thioethers) has received little at
209 the authors show a highly efficient route to fluorinated poly(aryl thioethers) via an organocatalyzed
210 erein, we report a highly efficient route to fluorinated poly(aryl thioethers) via an organocatalyzed
211 remarkable reactivity enable rapid access to fluorinated poly(aryl thioethers), but also opens new av
212 of the volatile catalyst and TMSF byproducts.Fluorinated poly(aryl thioethers), unlike their poly(ary
213  can be used as a monomer in vivo to produce fluorinated poly(hydroxyalkanoate) (PHA) bioplastics wit
214 ize polymer mechanochemistry to synthesize a fluorinated polyacetylene, a long-sought-after air-stabl
215 ion to give richly functionalized and highly fluorinated polyarenes.
216 ated by laser-desorption of the near-planar, fluorinated polycyclic aromatic hydrocarbon (PAH), C60H2
217 assembling giant surfactants consisting of a fluorinated polyhedral oligomeric silsesquioxane (FPOSS)
218                             By utilizing the fluorinated polymer (PBDB-TF) as the electron donor, the
219 luorocarbon emulsion polyplexes containing a fluorinated polymeric CXCR4 antagonist (F-PAMD) as an si
220  cleaved from the backbone of the side-chain fluorinated polymers coated on the fibers and then trans
221 hat, among others, degradation of side-chain fluorinated polymers in the environment and landfills ca
222 coated with perfluorohexane-based side-chain fluorinated polymers.
223  treated with fluorotelomer-based side-chain fluorinated polymers.
224 n of these molecules, leading to a series of fluorinated polysubstituted imidazoles in gram scale.
225 ailable fluorinated aromatic amino acids and fluorinated precursors as example applications of the me
226                                        These fluorinated probes each use two distinct visible wavelen
227 egarding the toxicity and adverse effects of fluorinated processing aids on humans and the environmen
228 E)-1,1,3,4-tetrafluorobutadiene as the major fluorinated product.
229 building blocks for the synthesis of various fluorinated products.
230 g multiple chain extensions to form multiply fluorinated products.
231 analogues thus expand the scope of available fluorinated proline analogues as tools to tailor proline
232                                              Fluorinated proline derivatives have found diverse appli
233 uous flow synthesis of highly functionalized fluorinated pyrazoles and pyrazolines has been developed
234 nteresting but yet mostly unknown classes of fluorinated pyrazoles are outlined.
235 ave led to the ever-increasing popularity of fluorinated pyrazoles in various areas of science are di
236                                              Fluorinated pyrazoles play an important role in medicina
237 w, analysis of novel synthetic approaches to fluorinated pyrazoles that appeared in recent years is p
238              In this work, we synthesized 15 fluorinated pyridine derivatives and tested their bindin
239 F(5)N, which results in the migration of the fluorinated pyridine moiety to the carbene ligand.
240                          Chemotherapy with a fluorinated pyrimidine and a platinum agent, followed by
241 observed in the presence of an electrophilic fluorinating reagent containing a weak N-F bond despite
242 e report the first practical use of SF6 as a fluorinating reagent in organic synthesis.
243 onyl oxygen atoms are proposed to direct the fluorinating reagent through C-H hydrogen bonds.
244 ing materials and effectively replaces harsh fluorinating reagents by a combination of oxalyl chlorid
245 g materials and 2) a dependence on hazardous fluorinating reagents such as XeF(2) .
246 s with either fluorinated building blocks or fluorinating reagents, new opportunities arise for the d
247                          We report a pair of fluorinated, redox-active copper complexes for potential
248 brid DSs mediated by the hybrid hydrogenated-fluorinated RHF Janus dendrimer.
249 lohexyl and linear aliphatic amines could be fluorinated selectively at the gamma-methyl and methylen
250 alic acid-dependent and was blocked with the fluorinated sialic acid mimetic Ac(5)3F(ax)Neu5Ac.
251 his, two cholesterol analogs with truncated, fluorinated side chains have been synthesized and shown
252                      In the environment, the fluorinated side chains will be slowly cleaved from the
253 ch possesses a flexible backbone with rigid, fluorinated side chains.
254                                        A new fluorinated silicon reagent bearing a functionalized tet
255 ce for forming cobalt-aryl bonds adjacent to fluorinated sites are the origin of the high regioselect
256 ne illustrates the potential ease with which fluorinated small molecules relevant to neuroscience dru
257 g the potential to generate a broad range of fluorinated small-molecule targets in living cells.
258 of the HFC solvent in tandem with the highly fluorinated, solubilizing, weakly coordinating [Al(OR(f)
259 y simply modulating the starting peptide and fluorinated solvent concentrations during synthesis.
260                            The presence of a fluorinated solvent is essential for the success of thes
261 omniphobic surface that can super-repel even fluorinated solvents, which highly wet all materials.
262 (19)F long-lived states in suitably designed fluorinated spy molecules allows one to perform competit
263                                        Using fluorinated starting materials, after mesylation, allowe
264 s is observed and calculated for planar ring-fluorinated stilbenes, trans-2,3,5,6,2',3',5',6'-octoflu
265  ) and difluoromethoxy (OCF(2) H) groups are fluorinated structural motifs that exhibit unique physic
266 tely new reactivities and thus also to novel fluorinated structural scaffolds.
267 luoroalkyl substances (PFASs) are a group of fluorinated substances of interest to researchers, regul
268                                         Five fluorinated substances were tentatively identified, and
269 yl)pyrrolidin-2-one derivatives, bearing the fluorinated substituent on a tetrasubstituted carbon.
270  presence of the highly electron-withdrawing fluorinated substituent, cyclic alpha-trifluoromethylate
271 e chemo- and stereoselective construction of fluorinated substituents, such as the trifluoromethyl (C
272 n, we employed (19)F NMR in conjunction with fluorinated substrate analogs to directly measure pK(a)
273 d herein, several alternative substrates and fluorinated substrate analogs were prepared to investiga
274                                         Less fluorinated substrates react slower.
275 describe the field of reactions of partially fluorinated substrates with transition metal atoms, ions
276 C-F bond cleavage has been shown to occur on fluorinated substrates.
277 e of substrates to give medicinally relevant fluorinated substructures with complete regiocontrol.
278  can be employed to synthesize unprecedented fluorinated sugars and steroids, and it can also be appl
279 lity, reactivity and interaction features of fluorinated sugars are described, as well as their appli
280 the oxygen-containing leaving group is not a fluorinated sulfonate such as triflate.
281 nly describes a new synthetic application of fluorinated sulfones, but also provides a new route to f
282    This work demonstrated the utilization of fluorinated sulfur ylides as versatile reagents for Core
283 ane at room temperature, gives rise to novel fluorinated tetrahydrofuran-fused tetrahydroquinolines i
284                                The resulting fluorinated tetrahydrofurans and pyrrolidines contain a
285 ction of beta-fluoroamine motifs featuring a fluorinated tetrasubstituted carbon.
286  for medicinal chemists to access a range of fluorinated therapeutic candidates with distinct physico
287  a wide bandgap polymer donor PM6 containing fluorinated thienyl benzodithiophene (BDT-2F) unit and a
288  The antiparallel self-assembled pore of the fluorinated tripeptides illustrates the selective ion-tr
289                                              Fluorinated tripodal compounds were recently reported to
290 metric properties of urea and thiourea-based fluorinated tripodal receptors are explored here for the
291 observed in the X-ray crystal structure of a fluorinated triterpenoid.
292 The aims of this study were to screen novel, fluorinated, TSPO radiotracers for susceptibility to the
293 n and metabolism of [(18)F]F-HPA-12, a radio-fluorinated version of the ceramide analog N-(3-hydroxy-
294              The four main sections describe fluorinated versions of alkyl, cyclic, aromatic amino ac
295 this protocol, we quantified the amount of a fluorinated xenobiotic (heptafluorobutyric acid, HFBA) i
296                                            A fluorinated xerogel composed of trimethoxymethylsilane a
297                                         This fluorinated xerogel screening layer can therefore be app
298 rodes covered with nickel porphyrin and this fluorinated xerogel.
299 onance imaging (iCEST MRI) and TF-BAPTA as a fluorinated Zn-binding probe with micromolar sensitivity
300 stances were tentatively identified, and non-fluorinated zwitterionic betaine compounds, which are co

 
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