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1 of 3,5-bis(het)arylisoxazoles, involving the reaction of 1,3-bis(het)arylmonothio-1,3-diketones with
3 etraphosphacyclooctadecanes via condensation reaction of 1,4-bis(organylphosphino)butane, formaldehyd
10 , we report a highly C3-selective allylation reaction of 1H-N-(benzoyloxy)indazoles using CuH catalys
12 aromatization/nucleophilic acyl substitution reaction of 2-(4-oxo-2-thioxothiazolidin-5-ylidene)aceta
13 H-pyrroles, prepared by the Ni(II)-catalyzed reaction of 2-(azidocarbonyl)-2H-azirines with 1,3-diket
14 precedented synthesis of quinazolines by the reaction of 2-aminobenzyl alcohol with primary amides.
16 hrough the dearomative (4 + 3) cycloaddition reaction of 2-vinylindoles or 4H-furo[3,2-b]indoles with
20 The observed behavior strongly contrasts the reaction of 9-EP on the chiral Pd(1) -terminated PdGa{11
22 al coordination solid 1(c) is synthesized by reaction of a bispyridyl dithienylethene (DTE) photochro
25 e the C6-N bond, a transannular Mannich-type reaction of a cyclic nitrone to stitch the C4 and C13 to
28 nvestigated the photochemical activation and reaction of a hydroxyquinone-derived phenyliodonium ylid
32 ort a new ligand to promote the transannular reaction of a range of fused- and bridged-bicyclic secon
34 he results indicate that a folding-unfolding reaction of a specialized temperature-sensitive structur
36 ate a spatially selective photocycloaddition reaction of a two-dimensional molecular network with def
37 the activation free energy for the unfolding reaction of ACBP without affecting the position of the t
40 zed, template-directed remote C-H activation reactions of alcohols, carboxylic acids, sulfonates, pho
41 SNs, catalyze the ring-opening hydroboration reaction of aliphatic and styrenic epoxides with pinacol
43 triplet excited-state [2 + 2] cycloaddition reactions of alkenes photocatalyzed by the QD through se
46 catalyzed oxidative C-C bond forming cascade reaction of allenes involving a coupling between an enal
47 ficient palladium-free Stille cross-coupling reaction of allylic bromides and functionalized organost
53 2)H(3))(2)] (3e) have been isolated from the reaction of Ar(F)-Bpin with Pd(OAc)(2) in acetonitrile s
54 sequencing and quantitative polymerase chain reaction of archaeal and bacterial nitrogen cycling gene
55 ate (TMSOTf)-promoted intermolecular cascade reaction of aromatic diazo ketones with olefins has been
56 two bioorthogonal reactions-the condensation reaction of aromatic nitriles and aminothiols and the in
59 simple and efficient sulfa-Michael addition reaction of aryl thiols to trisubstituted alpha-fluoro-a
61 the limitations of sigmatropic rearrangement reactions of aryl allyl anilines, which deliver exclusiv
62 s (TRAMs) in moderate to good yields via the reactions of aryl boronic acids and ortho-hydroxyarylald
63 We demonstrate the metal-free alkenylation reactions of aryl esters with alpha-diazoesters to give
64 re achieved for 31 examples in S-H insertion reactions of aryl thiols and alpha-carbonyl sulfoxonium
67 hium cation Li(+)-catalyzed Diels-Alder (DA) reactions of benzene toward a series of acetylenes of im
68 ent study, we investigated the aqueous phase reactions of benzoic acid with sulfite in the presence o
69 o-2H-naphtho[1,2-b][1,4]oxazin-2-ones by the reaction of benzoxepine-4-carboxylates with chiral amino
74 with molar yields of 0.01-0.03% from aqueous reactions of biogenic SOA generated by (*)OH photooxidat
75 curbit[7]uril (CB7) catalyzes the hydrolysis reaction of bis(4-nitrophenyl)carbonate (1) but inhibits
78 PPQV2, via the Horner-Wadsworth-Emmons (HWE) reaction of C(2) -symmetric 1,4-bis(diethylphosphonometh
80 (MoBA) ligands have been synthesized by the reaction of C(alpha),C(ortho)-dilithiated phosphazenes w
83 identifies a crystalline phase of CaO(3) by reaction of CaO and O(2) at high pressure and high tempe
84 f acyl fluorides using the deoxofluorination reaction of carboxylic acids using XtalFluor-E is descri
85 ask activity, catalyzing the transvinylation reaction of carboxylic acids without losing their origin
87 orine isotope fractionation was detected for reaction of CH(3)Cl with (.)OH and (.)Cl radicals, where
91 bond coupling in Y-DeAlBEA proceeds via the reaction of coadsorbed acetaldehyde and ethanol to form
94 boronate complexes are readily generated by reaction of commercial bis(pinacolato)diboron with alkyl
98 CuSeO to Cu(2) Se, obstructing the reduction reaction of Cu(+) into Cu metal at the interface and hen
100 esized with a broad substrate scope from the reaction of cyclic 1,3-dienyl boronic esters with arylni
103 Sn atoms catalyze the transfer hydrogenation reaction of cyclohexanone in a 2-butanol solvent 10x fas
104 ,2-trifluoroacetophenone and the Diels-Alder reaction of cyclopentadiene with methyl vinyl ketone.
105 ed-shell singlet species from the reversible reactions of cyclotrisilene c-Si(3) Tip(4) (Tip=2,4,6-tr
106 hensive treatise on the catalytic asymmetric reactions of deconjugated butenolides reported so far.
109 tly, visible light-promoted carbene transfer reactions of diazo compounds via free carbene intermedia
111 tic isotope effect (k(H) /k(D) =5.7) for the reactions of diphenyl ether under H(2) and D(2) atmosphe
112 mentation using hypervalent iodine reagents, reactions of donor-acceptor cyclopropanols, and pericyli
113 mol blue, methyl red, and resazurin, and the reactions of each system with H(2) in the presence of Au
116 thways from C1 -> H1 involve the bimolecular reaction of EHP with different atmospheric species.
118 est that connexins are involved in the early reaction of ependymal cells to injury, representing a po
119 While writing a comprehensive review on the reactions of epoxides with titanium(III) reagents, we en
121 me luminescence are generated in situ by the reactions of Eu(TTA)(3)(H(2)O)(2) with LFM components.
124 r reveal the potential for complexity in the reaction of formaldehyde with biomedicinally relevant mo
125 nd gamma-, delta-, and epsilon-lactonization reactions of free carboxylic acids enabled by a novel cy
126 here the intermolecular metal-free addition reaction of functionalized benzyl halides to aldehydes u
127 and in situ formed 1-aza-1,3-dienes from the reaction of furan/pyrrole/thiophene and PhINTs for the r
128 This study investigated the lipid oxidation reactions of furan fatty acids, long-chain omega-3 polyu
129 of heterogeneous chemical kinetics with the reaction of gas phase O(3) and aqueous maleic acid dropl
130 ch contrasts most transition-metal-catalyzed reactions of gem-difluoroalkenes that typically involve
135 er-irradiated region, leads to the selective reaction of graphene, thereby completing direct laser wr
136 cycloisomerization to a cyclohexadiene, is a reaction of great historical and practical significance.
137 It was found by us that the P-C coupling reaction of >P(O)H reagents with PhX (X = I and Br) in t
142 otoredox-catalyzed alpha-amino C-H arylation reaction of highly substituted piperidine derivatives wi
144 an alternative mechanism, in which the major reaction of HO(.) with dG was proposed to involve hydrog
147 More complex kinetics were observed for the reactions of imidazolidinones and several pyrrolidines c
148 hannel diffusion) in the enzymatic multistep reactions of individual PCE-RdhAs rather than different
149 m-catalyzed, three-component carbosilylation reaction of internal symmetrical alkynes, silicon electr
150 display superior catalytic reactivity in the reaction of isocyanates with alcohols and the aza-Morita
153 nalysis of redox equilibria arising from the reaction of (L)Pd(OAc)(2) and hydroquinones (L = bathocu
158 gamolecules are assembled through sequential reactions of linkers that present irreversible inhibitor
161 cle composition for various electrooxidation reactions of liquid fuels (formic acid, methanol, and et
163 C(6) H(3) )NC(Me)}(2) CH), was isolated via reaction of [(Me) LZnSCPh(3) ] (1) with 2.3 equivalents
166 forming regions via the elementary gas-phase reaction of methylidyne radicals with hydrogen sulfide,
167 tallic titanium frameworks by metal-exchange reactions of MOF crystals at temperatures below those co
168 rous media drives the transport, mixing, and reaction of molecules, particles, and microorganisms acr
171 use, we applied this approach to a cellular reaction of multidrug resistance (MDR) transport, which
173 readily prepared by the iodocyclocarbamation reaction of N-allylated N-aryl or N-heteroaryl carbamate
174 ted tetrahydropyrroloisoindolone via Mannich reaction of N-propargyl amido alcohols with 1,3-dicarbon
175 a radical-mediated reductive epoxide opening reaction of N-tethered epoxy-indoles that trigger facile
176 are the Rh(III)-catalyzed cascade annulation reactions of N-(pivaloyloxy)benzamides with 1,5-enynes t
177 phide, that may be prepared either by direct reaction of NaPH(2) with carbon dioxide or by hydrolysis
179 the cap loop which modulates the association reactions of nDsbD with its partners resulting in optimi
180 PMe(3), are unique in promoting preferential reaction of Ni(0) with aryl tosylates and other C-O bond
181 introduction of ammonia (NH(3)), during the reaction of NO indicating a divergence from current lite
187 s are implicated in a multitude of oxidative reactions of organic substrates, as well as in catalytic
188 tigate single-electron transfer (SET) in the reactions of organomagnesium reagents with carbonyl comp
193 general assignment of reactive positions for reactions of ozone with aromatic carbons in ortho-, meta
194 a comparative study of the electron-induced reaction of pentyl bromide (PeBr) and phenyl bromide (Ph
195 X/6-31G(d,p)//PCM(MeCN) calculations for the reaction of Ph(2)P(O)H and PhX revealed a favorable ener
198 n phosphorus and gallium were synthesized by reaction of (phosphanyl)phosphaketenes with the gallium
199 ess is demonstrated via the charge inversion reaction of phosphatidylcholine (PC) lipid cations gener
200 major approaches were selected: (1) the Stec reaction of phosphorus amides with carbon disulfide; and
201 mation of an intermediate radical anion upon reaction of photogenerated holes with an electron donor,
202 s of the kinetics of the forward and reverse reactions of photooligomerization of Arabidopsis CRY1 an
205 an increase in pH, which was related to the reaction of protonated Fe(VI) species (HFeO(4)(-)) with
206 experiments based on gas-phase ion-molecule reactions of protonated model compounds were successfull
209 styrene derivatives, synthesized through the reactions of readily accessible feedstock olefins with b
210 ctivating enzyme (E1)-catalyzed condensation reaction of recombinant Ub precursors to give various ho
211 in rhodium diethylene complexes, made by the reaction of Rh(eta(2)-C(2)H(4))(2)(acetylacetonate) with
213 ide, for asymmetric tandem oxa-Michael-Henry reaction of salicylaldehyde with conjugated nitroalkene
215 the addition of one nucleotide in a one-pot reaction of sequential coupling, oxidation, and deprotec
220 locks, were synthesized in high yield by the reaction of sodium azide with 2H-azirine-2-carbonyl chlo
221 This review describes the gold-catalyzed reactions of specially activated alkynes, allenes, and a
222 catalyst for enantioselective hydroboration reaction of substituted ketones, and the corresponding s
223 ol for the Pd(II)-catalyzed C-H alkenylation reaction of substituted N-allylanilines via an unusual 6
226 of a fluoride leaving group (LG) in covalent reactions of sulfonyl fluorides and arylfluorosulfates.
228 ve sites in UiO-66 become accessible for the reaction of TBA, with the activity depending on the dens
231 14) ) is unraveled by probing the elementary reaction of the 2-tetracenyl radical (C(18) H(11) (.) )
232 )]-C=CAr (Ar = 2,6-Cl(2)C(6)H(3)) forms upon reaction of the alkyne H-C=CAr with the copper(II) tert-
234 to the established hydrolysis products, the reaction of the class D nucleophilic serine beta-lactama
236 e HE anion can be easily prepared in situ by reaction of the corresponding HE with KO(t)Bu in DMSO at
237 Bu)(2)], has been synthesized from the redox reaction of the dipotassium bis(silylenyl)-nido-carboran
238 ation size mismatch, which also promotes the reaction of the dopant with O(2) from the gas phase.
239 omplex with nitroaromatic explosives through reaction of the enolate ion of 3-mercapto-2-butanone.
240 ents taking place in the early stages of the reaction of the ependyma to injury remain little underst
241 measured the light signal resulting from the reaction of the HRP-labelled anti-human IgA with a H(2)O
242 rface and the Li(2)O formation caused by the reaction of the intercalated lithium with the residual o
244 nt N-substituents was prepared by the direct reaction of the lithium salt of N-heterocyclic imine (NH
245 hat the vinyl azide formed by competitive E2 reaction of the mentioned triflate was an interesting pr
246 een synthesized via the elementary gas-phase reaction of the methylidyne radical (CH) with the benzen
249 eavage, but it also induces a face-selective reaction of the olefin of the allylic group, leading to
251 s a rich reactivity towards small molecules; reaction of the P(2) species with CO(2), water or a bora
252 esults: (+/-)-(11)C-YJH08 was synthesized by reaction of the phenolic precursor with (11)C-methyl iod
255 ailed computational study of the atmospheric reaction of the simplest Criegee intermediate CH(2)OO wi
256 HHM hydrolysis is caused by a heterogeneous reaction of the solid Hf(18) cluster, and not from small
257 at an in situ-induced direct desulfurization reaction of the thiophene moiety strongly improves the m
260 nce of a W=O moiety arising from the in situ reaction of the W=C(t)Bu functionality with the coordina
262 induces changes to the photosynthetic light reactions of the chloroplasts it steals from the alga Ac
263 C1q globular heads initiates the downstream reactions of the complement cascade ultimately resulting
264 (thf)(n) (M=Ca, n=2; M=Sr, n=3), through the reactions of the corresponding bis(amides), M{N(SiMe(3)
265 at higher states-of-charge, indicating that reactions of the electrolyte at the positive electrode a
268 been studied in-depth through stoichiometric reactions of the key diazatitanacyclohexadiene intermedi
273 e could be identified separately and further reactions of these species at the opposite electrode pre
274 we show that the conformationally orthogonal reactions of these two carbasugars reveal mechanistic de
277 for organofluorine chemistry; however, most reactions of this substructure proceed through reactive
278 ifferent products could be isolated from the reaction of three CO(2) molecules with both Si=C bonds.
279 Enabled by the highly stereocontrolled aldol reactions of three chiral ketone building blocks, an eff
282 interactions to enforce stereoselectivity in reactions of transient and highly reactive open-shell in
283 ition and reductive elimination are defining reactions of transition-metal organometallic chemistry.
284 signals were exploited to monitor the rapid reaction of tris(tert-butoxy)silanol with triflic anhydr
285 steps: (a) a regioselective Pictet-Spengler reaction of tryptamine with 2,3-pentanedione; (b) a chem
287 Pd(0) -catalyzed asymmetric [4+3] annulation reaction of two readily accessible starting materials ha
289 ical method for the synthesis of amines, but reactions of unactivated alkenes remain inefficient.
290 r N-heterocyclic carbenes (NHCs) has enabled reactions of unactivated alkyl electrophiles not only li
292 stituted type I porphyrins that utilizes the reaction of unsymmetrical 3,4-difunctionalized pyrroles
294 In contrast to the reaction in THF, the reaction of [UO(2)(N(SiMe(3))(2))(2)(THF)(2)] with Cy(7)
297 l-Crafts-type coupling and dedinitrogenation reactions of vinyldiazo compounds with aromatic compound
298 ction (OER) is the performance-limiting half reaction of water splitting, which can be used to produc
299 n with first-principles calculations we find reactions of xenon with recently discovered iron peroxid