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1 cid adenine dinucleotide at the adenosine 3'-hydroxyl group.
2 e ring to substitute the amino group with an hydroxyl group.
3 ies on the carbon position of the acyl chain hydroxyl group.
4 at funnels to its narrowest region at the C3-hydroxyl group.
5 tated by the electron-donating nature of the hydroxyl group.
6 res that are highly stable because of the 2'-hydroxyl group.
7 ylation at a secondary C-H bond gamma to the hydroxyl group.
8 r connecting the metal chelating unit to the hydroxyl group.
9 on despite containing the equivalent of a 3'-hydroxyl group.
10 rogen bonded to this residue via its 17alpha-hydroxyl group.
11 ion of proteins at the Ser or Thr side chain hydroxyl group.
12 te)s with a functionalizable pendant primary hydroxyl group.
13 ng a side-arm and a potentially nucleophilic hydroxyl group.
14 phile by a hydrogen bond from the catalyst's hydroxyl group.
15 vel polar interaction mediated by the RJW100 hydroxyl group.
16 s achieved with the substrate bearing a free hydroxyl group.
17 ase yielding an intermediate with a tertiary hydroxyl-group.
18 s acidic surface domains depleted in surface hydroxyl groups.
19 ,3-dioxane structures with lignin side-chain hydroxyl groups.
20  hydration or the number of crystallographic hydroxyl groups.
21 f kanamycin B analogues alkylated at various hydroxyl groups.
22  undergo acid-base chemistry with the silica hydroxyl groups.
23 ive exchange of C-H protons adjacent to free hydroxyl groups.
24 ions because of the presence of aldehyde and hydroxyl groups.
25 avenging activity, due to the high number of hydroxyl groups.
26  hydrogen originates exclusively from glycol hydroxyl groups.
27 oxide thin film with a controlled density of hydroxyl groups.
28 esistance to fouling after the activation of hydroxyl groups.
29  fragmentation occurs even in the absence of hydroxyl groups.
30 ction processing of substrates with inverted hydroxyl groups.
31 thiiranium ions in competition with phenolic hydroxyl groups.
32 especially those that lack adjacent aromatic hydroxyl groups.
33 saccharides, and saccharides containing free hydroxyl groups.
34 f detected metabolites were those containing hydroxyl groups.
35 hanism with participation of the most acidic hydroxyl groups: 7-OH in SIL and 7-OH and 3-OH in DHS.
36  trisubstituted alkenes was achieved through hydroxyl group activation, an approach that also enables
37                    Activation of the epsilon-hydroxyl group allowed cyclization to either the corresp
38 s hexaketide with an epimerized nucleophilic hydroxyl group allowed for direct evaluation of the subs
39 cacy for the selective oxidation of a single hydroxyl group among many in unprotected polyol natural
40 work are proposed for arsenic species, i.e., hydroxyl group and benzenedicarboxylate ligand.
41 concurrent with G40(N1) moving closer to the hydroxyl group and directing the in-line attack.
42 se only compounds that contain a carboxyl or hydroxyl group and have moderate steric hindrance were e
43 tabilized by hydrogen bonds between the 5-HT hydroxyl group and lipid headgroups and allows 5-HT to i
44 ly suggest that hydrogen bonding templates a hydroxyl group and Pd addition across the alkene and pro
45 xtensive interactions between each trehalose hydroxyl group and residues of the cap and core domains
46  of the propeptide by deprotonating the Thr1 hydroxyl group and that both residues together with Asp1
47  pocket and interactions between the allylic hydroxyl group and the BTN3A1 backbone.
48 the noncovalent interaction of the substrate hydroxyl group and the chiral cationic palladium catalys
49 duct selectivity originating from a resident hydroxyl group and the critical choice of the reaction s
50 duces ligand formation between oxygen on the hydroxyl group and the zinc ions, which expands the stab
51 ning initiated by the attack of one phenolic hydroxyl group and, then, by addition of one aromatic ph
52  anthocyanidins is greatly affected by the 3-hydroxyl group and/or a catecholic moiety.
53 sence of other functionalities, such as free hydroxyl groups and amines widely present in biological
54                       However, the number of hydroxyl groups and in particular the presence of the ca
55  followed by peracetylation of the remaining hydroxyl groups and separation of isomers resulted in th
56  trimetaphosphate to triphosphorylate RNA 5'-hydroxyl groups and suggested that RNA world organisms c
57 ces, but it is not well-understood how these hydroxyl groups and their distribution on a surface affe
58 ugh the chemical exchange of protons between hydroxyl groups and water.
59 eroid "reduced pregnenolone" (containing two hydroxyl groups) and its d4-analogue provide evidence of
60                               Its equatorial hydroxyl groups are hydrogen-bonded directly to the enzy
61 orm of carboxyfluorescein in which 3' and 6' hydroxyl groups are masked as acetate esters (CFDA).
62                                        Ortho-hydroxyl groups are necessary to promote the nucleophili
63                                              Hydroxyl groups are widely found in bioactive molecules
64 thesized was related to the structure of the hydroxyl group array in sucrose.
65 in situ intramolecular oxacyclization by the hydroxyl group as a pre-existing nucleophile of the alco
66  of a fluorine atom adjacent to the phenolic hydroxyl group as in 3w, 3z, 3aa, and 3bb to strengthen
67 we identify the coverage of reactive surface hydroxyl groups as a suitable descriptor for the OER act
68 0, IC50 = 11 muM) revealed the importance of hydroxyl groups as hydrogen-bond donors for PXR antagoni
69 pH of the media maintains the ammonium and p-hydroxyl groups as their conjugate acids.
70  titania likely donates protons from surface hydroxyl groups as well as supplying electrons and holes
71 ium group is lower than that of the phenolic hydroxyl group, as is the case for the alpha-amino-prote
72 ective reductive intramolecular cyclization, hydroxyl group-assisted in situ N-Boc-deprotection, sele
73 ing, or minimally the stereochemistry of the hydroxyl group at C-16, is crucial for the activity of P
74 lyzed oxidation can single out the secondary hydroxyl group at C3 in glucose, circumventing the more
75                          It was found a free hydroxyl group at C3 of the 2-deoxy-sugar-derived lactol
76 aCaT keratinocytes, suggesting the lack of a hydroxyl group at C44 as a critical feature for PLTXs cy
77 onium moiety appeared more proficient than a hydroxyl group at directing the stereochemical course of
78 4 belongs to the SDR family and oxidizes the hydroxyl group at position 17 of estradiol and 5-androst
79                     These data show that the hydroxyl group at position 3 contributed significantly t
80                      This indicates that the hydroxyl group at position 3 in PQS is essential and tha
81  efficiently coupled at -40 degrees C to the hydroxyl group at position 3 of glucopyranosyl acceptors
82 e inhibitory activity of arginase, while the hydroxyl group at position 5 did not.
83  analogues of corticosteroid drugs bearing a hydroxyl group at the C19 position.
84       Correlation analysis revealed that the hydroxyl group at the R'4 position of the flavonoids con
85                   Thus, introducing a single hydroxyl group at the Valpha/Vbeta interface, at a signi
86 itable for the introduction of the requisite hydroxyl groups at carbons 4a and 12a.
87  stability to post-translationally installed hydroxyl groups at position 4 of prolyl residues.
88 nts, a 2-fluoro substitution, and additional hydroxyl groups at positions 3' and 4'.
89 the inter- or intramolecular reaction with a hydroxyl group belonging to an alcohol, a phenol or an a
90 modulators BPAM97 (2) and BPAM344 (3) into a hydroxyl group (BPAM557 (4) and BPAM521 (5), respectivel
91 ylation of acceptors with more than one free hydroxyl group by 2,3,5,6-tetrabenzoyl galactofuranosyl
92 ilitated by the coordination of the reactive hydroxyl group by Ca(2+) in the active site, lowering th
93 ate that results from deprotonation of the 5-hydroxyl group by histidine-267.
94                            That is, a remote hydroxyl group can play a larger role in binding than tw
95 thered primary, secondary, and tertiary free hydroxyl groups can all react to give the corresponding
96  show that molecules containing at least two hydroxyl groups can be converted into methanol, which de
97 xygenated hydrocarbons that bear one or more hydroxyl groups comprise a large set of natural and synt
98  for example, CH(2)-units, aromatic rings or hydroxyl groups, contribute differently to the sorption
99 dation reactions and the presence of vicinal hydroxyl groups correlated with flavonoid reactivity in
100                          The total number of hydroxyl groups correlated with the ability of flavonoid
101 6 dyad, proposed to be involved in substrate hydroxyl group deprotonation, a critical requirement for
102                          Reactions involving hydroxyl group derivatization with a variety of electrop
103 ic acid feet, and "steps" along an isotactic hydroxyl-group-derivatized polyether track by the format
104 y the axial or equatorial orientation of two hydroxyl groups differentiating among these isomers in t
105                In contrast, methylation of a hydroxyl group enhanced the binding at acidic pH, whilst
106 proton of the phosphinic acid protonates the hydroxyl group, enhancing the leaving group ability.
107 llowed by epoxidation on the face syn to the hydroxyl group exclusively; reduction then provided eith
108           Successful differentiation between hydroxyl groups features the selective acylation of prim
109 ments revealed a crucial role of the pendent hydroxyl groups for catalytic activity.
110                                              Hydroxyl groups form strong hydrogen bonds to water mole
111 acent Au sites was apt to react with surface hydroxyl groups formed from water splitting, leading to
112 -ray quality crystals of five compounds with hydroxyl groups forming five- and six-membered chelation
113  coordinate bonds with the zinc ion, and the hydroxyl group from CQ formed an effective hydrogen bond
114                       O-Alkylation of the C3 hydroxyl group generated novel 3-O-functionalized Neu5Ac
115 ated by the stereoselective incorporation of hydroxyl groups, generating cis-4- and cis-5-aminocyclop
116 uch bicyclic compound carrying an equatorial hydroxyl group has activity equal to that of the parent
117 drophobic substituents are attached to the 6-hydroxyl groups, has been the subject of speculation.
118 h cleave a methylenedioxy bridge leaving two hydroxyl groups, have previously not been reported in pl
119 lics was evaluated in model solutions, where hydroxyl groups, hydrophobic bonding and steric hindranc
120 sing because of the directing influence of a hydroxyl group in C horizontal lineC bond hydrogenation.
121 refore, the selective conversion of a single hydroxyl group in natural products into a ketone would e
122 s efficiently prevented by deprotonating the hydroxyl group in position 2 of the glyconitriles during
123 tes are open enough to accommodate the extra hydroxyl group in RNA, further supporting our conclusion
124                  Of particular interest is a hydroxyl group in the 4' position 2a which induced a pre
125 d by the enzyme or the replacement of the C3 hydroxyl group in the natural substrate by an amino grou
126 distance from the aromatic ring, whereas the hydroxyl group in the para-position is not essential, bu
127                                        The 3-hydroxyl group in the sphingoid base of sulfatides offer
128 rogen (D/H) ratio in strongly bound water or hydroxyl groups in ancient martian clays retains the imp
129  was associated with carboxylic and phenolic hydroxyl groups in biochars BP300-450, whereas 91% of so
130          Site-selective functionalization of hydroxyl groups in carbohydrates is one of the long-stan
131 trolled subtle reactivity differences of the hydroxyl groups in carbohydrates were utilized to quickl
132 logs revealed the co-operative nature of the hydroxyl groups in mediating both this aqueous glycosyl
133 s, indicating a high impact of the number of hydroxyl groups in the anthocyanin B-ring.
134 of compound 3, focusing on the carbamoyl and hydroxyl groups in the distal and proximal phenyl rings.
135                             The free primary hydroxyl groups in the metal-organic framework of CDMOF-
136  proceeds in sequential steps related to the hydroxyl groups in the three aromatic rings.
137 mpared with the aim of investigating how the hydroxyl groups in their structures govern the biologica
138 ioxidant capacity because of the presence of hydroxyl groups in various configurations and numbers wi
139 le of the serine 364, and more precisely its hydroxyl group, in coupling sodium and substrate fluxes.
140 er, RdmB, it catalyzes the introduction of a hydroxyl group, in the case of NDUFAF5, into Arg-73 in t
141  RNase H2 to selectively create ligatable 3'-hydroxyl groups, in contrast to alternative methods that
142 ) decreases their vapor pressure as a second hydroxyl group is incorporated to accelerate their oxida
143 icting common sites of UGT conjugation, like hydroxyl groups, it can also accurately predict the gluc
144 thyris ADH1 catalyzes dehydrogenation of the hydroxyl groups, leading to the subsequent rearrangement
145 ded to the calcite surface through its polar hydroxyl group, leaving the hydrophobic ends of the etha
146                              Conversion of a hydroxyl group located close to the nitroxyl moiety succ
147 atalytic function is to lower the pKa of the hydroxyl group, making it a highly effective nucleophile
148                                 Conventional hydroxyl group manipulation in the latter and products o
149 ts suggested that the number and position of hydroxyl groups may increase or decrease the protective
150 bicyclic ring I carrying equatorial amino or hydroxyl groups mimicking the bound side chains of neomy
151 Dandante or amine NDamine, carboxyl NDvox or hydroxyl groups NDH and drop-casted or spray-coated onto
152                      Additives with multiple hydroxyl groups, nonlinear molecule, and electric charge
153 (L)], in which deprotonation of the bridging hydroxyl groups occurs.
154 und useful in the in situ blocking of the C3-hydroxyl group of 2,4-di-O-TBDPS protected 1,6-anhydrogl
155  side-chain hydroxyl group of Ser-497 to the hydroxyl group of 5, whereas the unfavorable entropy mig
156 e orientation of Ser-497 pointing toward the hydroxyl group of 5.
157                                 However, the hydroxyl group of 5hmC and carbonyl group of 5fC face to
158 -triphosphate (2'-Az-dATP) onto the tyrosine hydroxyl group of a peptide, which is either tethered to
159 ron ion (Fea), which is proposed to bind the hydroxyl group of a postulated intermediate in the last
160  calculations reveal that protonation of the hydroxyl group of aliphatic alcohols transforms the C-O
161 catalytic base and deprotonates the reactive hydroxyl group of caffeoyl-CoA.
162 rase responsible for methylation of the meta-hydroxyl group of caffeoyl-coenzyme A (CoA) on the pathw
163                                Replacing the hydroxyl group of choline with different substituents, s
164                                          The hydroxyl group of enantioenriched benzyl, propargyl, all
165            Furthermore, either the 2'- or 3'-hydroxyl group of GDP was found to be required for effic
166 ons suggest that a hydrogen bond between the hydroxyl group of Hzp and a backbone amide carbonyl posi
167 m (Sorghum bicolor; SbCOMT) methylates the 5-hydroxyl group of its preferred substrate, 5-hydroxyconi
168 tiated through the deprotonation of the para-hydroxyl group of monolignols.
169 olecular dynamic analysis indicated that the hydroxyl group of monophenolic substrates can bind to Cu
170 owth, characterized by acetylation of the C6 hydroxyl group of N-acetylmuramic acid in the PG glycan
171 ation of a hydrogen bond from the side-chain hydroxyl group of Ser-497 to the hydroxyl group of 5, wh
172 thiol of cysteine and O-glycosylation of the hydroxyl group of serine in peptide substrates.
173 covalent attachment of sugar moieties to the hydroxyl group of serine or threonine on proteins/peptid
174 tomyces venezuelae is able to oxidize the C3 hydroxyl group of TDP-D-quinovose to the corresponding k
175 tributed to a much stronger H-bond between a hydroxyl group of TETROL and the carbonyl group of the (
176 300(Sc), I2(I), is located near the bridging hydroxyl group of the [ScO4(OH)2] moiety [I2(I)...H-O =
177 vity for the glycosylation on the equatorial hydroxyl group of the acceptor was obtained thanks to th
178  Asp(A117) determines the orientation of the hydroxyl group of the acyl-CoA esters by H-bond formatio
179 onyl group and decreased the basicity of the hydroxyl group of the CF3 amino alcohol formed.
180  of cyclodextrin of CD-MOFs and the phenolic hydroxyl group of the curcumin.
181 ation can be prevented by methylation of the hydroxyl group of the flavonoids.
182 -terminal phosphates is selective for the 2'-hydroxyl group of the latter.
183  core, stereocenters at C14 and C15, and the hydroxyl group of the m-tyrosine (m-Tyr) residue as key
184 transfer of the methyl group from SAM to one hydroxyl group of the myricetin in a cation-dependent ma
185         This binding mode would place the C5 hydroxyl group of the postulated final intermediate dist
186 acidic residues, water molecules, and the 3'-hydroxyl group of the primer so that the A metal is in a
187 imary amine accepts a hydrogen bond from the hydroxyl group of the reactant have been modeled.
188 r attachment of fluoride anion to a specific hydroxyl group of the steroid.
189 lving a proton shuttle mechanism through the hydroxyl group of the sugar and a water molecule.
190 elA binds the CCA tail to orient the free 3' hydroxyl group of the terminal adenosine towards a beta-
191                                        The N-hydroxyl group of this motif is highly subject to sulfat
192 esis and by seeing close contact between the hydroxyl group of this residue and the azaribose moiety
193                          The position of the hydroxyl group of Tyr-166 and an observed shift in the p
194                                          The hydroxyl group of Tyr67 sits 3.6-4.0 A from the nearest
195                    The results show that the hydroxyl groups of (2S)-hesperetin are important for inh
196 tive site has an open structure and that the hydroxyl groups of all xylose residues in the active sit
197 ak reversible covalent bonds between vicinal hydroxyl groups of arabitol and boronic acid substituent
198 as been synthesized by connecting the tailed hydroxyl groups of C-propan-3-ol pyrogallol[4]arene with
199 erial cellulose nanopaper are reduced by the hydroxyl groups of cellulose nanofibers, acting as the r
200 audanosoline, and O-methylated the 3' and 4' hydroxyl groups of certain alkaloids.
201 ta, a benzyl etherification of nonesterified hydroxyl groups of glycerol and hydroxy fatty acids was
202 (2) bonds and removes some of the oxygen and hydroxyl groups of GO, which initiates the evolution of
203 (2+) ions are bridged by the carboxylate and hydroxyl groups of lactate and the carboxylate group of
204                                          The hydroxyl groups of naphthol and tautomerizable phenol de
205  intermolecular hydrogen bonding between the hydroxyl groups of QC and PG.
206 bohydrate post-translational modification on hydroxyl groups of serine and/or threonine residues of c
207  which involves the attachment of glycans to hydroxyl groups of serine or threonine residues.
208 acetylglucosamine (O-GlcNAc) sugar moiety to hydroxyl groups of serine/threonine residues of cytosoli
209                        During oxidation, the hydroxyl groups of starch molecules are first oxidized t
210 olecular hydrogen bonding occurs between the hydroxyl groups of the binaphthols.
211 y synthesizing phosphoramidites in which the hydroxyl groups of the cross-linked product were orthogo
212 that tetrahedral [Zn(NH3)4](2+) ions bind to hydroxyl groups of the film at a stoichiometric ratio of
213 c apolar pocket that surrounds the C4 and C5 hydroxyl groups of the natural substrate, cause the open
214 rst time, and surprisingly only two of three hydroxyl groups of the neutral aliphatic triols are foun
215                                          The hydroxyl groups of the phosphonates and pyrrole -NH prot
216 ydrogen bonding that involves the side-chain hydroxyl groups of the serine.
217            Finally, increasing the number of hydroxyl groups of the steroid was sterically unfavorabl
218 on product depend on the substituents on the hydroxyl groups of the tartaric acid scaffold.
219 ds Asp(228), Asp(229), and Arg(226), and the hydroxyl groups of xylose.
220 ed the differentiation between the secondary hydroxyl groups OH-3 and OH-5 of 1,2-cis or 1,2-trans d-
221 oordination of calcium by the two equatorial hydroxyl groups, OH3 and OH4, at the non-reducing end.
222                In addition, we show that the hydroxyl group on MftA Tyr-30 is required for MftC catal
223                The analogues with a terminal hydroxyl group on the alkyl chain were efficiently fluor
224  determine the effect of the position of the hydroxyl group on the antioxidant properties of flavonoi
225  were identified as hydroxylated TBPH with a hydroxyl group on the aromatic ring.
226      As a result, the introduction of a meta hydroxyl group on the C4 anilino ring was computed to be
227 s reveal mechanisms by which the sacrificial hydroxyl group on the chromanol group can trap lipid per
228 ading structural model predicts that the C2' hydroxyl group on the mycosamine appendage is critical f
229 of ATP demonstrated the importance of the 2' hydroxyl group on the ribose ring in determining agonist
230                                        The 4-hydroxyl group on the thiazine ring partners with Ser-53
231 w)/M(n) < 1.2), bearing precisely one or two hydroxyl groups on one chain end and optionally a dye-la
232 le protection against stimulating effects of hydroxyl groups on P-gp-mediated transport.
233  WASP, where the number and configuration of hydroxyl groups on the acyl side chain impacted the degr
234 idues as well as changes in the positions of hydroxyl groups on the beta-side of the steroid core of
235 photoelectron spectroscopy revealed that the hydroxyl groups on the GONR were removed by the reductiv
236 d (FTIR) spectroscopy suggested more surface hydroxyl groups on the NCC than the MCC particles and co
237  in the gas phase, which also coadsorbs with hydroxyl groups on the Pt(557) surface.
238    The effects of the third "noninteracting" hydroxyl groups on the structures and binding constants
239 tify the favoured path, either through the 3-hydroxyl group or through the catecholic moiety in a ser
240 presence of specific chemical groups such as hydroxyl groups or hydrogens.The synthesis of two-dimens
241   Structural characteristics (positioning of hydroxyl group) or partitioning behaviour between the em
242  Bronsted acid catalysis, and the catalyst's hydroxyl group orients the thiolate nucleophile.
243  utilizes molecular oxygen as source for the hydroxyl group oxygen of 2-Hyp.
244 c site and further demonstrates that the A76 hydroxyl groups participate in post-transfer editing onl
245                 To set the desired amino and hydroxyl group pattern of the target, we designed a conc
246                                 Thus, the C3-hydroxyl group plays an important role in AmB ion channe
247 y the trans-azobenzene molecule with the two hydroxyl groups pointing into opposite directions is ads
248              Selective unmasking of a single hydroxyl group precedes solid-phase synthesis of one arm
249        Our technique is compatible with free hydroxyl groups present in the substrate.
250   Additionally, other extra-lattice aluminum hydroxyl groups previously discussed in the literature b
251 charides, deoxysugars, saccharides with free hydroxyl groups, pyranose, and furanose substrates.
252 of the diaxial conformation of the C4 and C5 hydroxyl groups recognized by the enzyme or the replacem
253                                Specifically, hydroxyl groups reduce the hydrophobicity of methyl-term
254 ylate group and a singly coordinated surface hydroxyl group, releasing an H2O molecule.
255 he formation of oligomers with the secondary hydroxyl group remaining nonesterified.
256  glycerol cluster indicate that the glycerol hydroxyl groups reorient around the Na atom as it makes
257          JDTic analogues 4-15 which have the hydroxyl groups replaced with other groups were synthesi
258 this phenomenon, a lead compound FG03 with a hydroxyl group replacing the 3''-NH2 group of kanamycin
259 nformations in which hydrogen-bonding to the hydroxyl group results in direction of the epoxidation t
260 The data suggested that compounds having a p-hydroxyl group showed moderate 2,2-diphenyl-1-picrylhydr
261 we have designed a new crown ether with four hydroxyl groups strategically positioned.
262 tent of halogenation and the position of the hydroxyl group strongly affected binding.
263  the derivatives of flavonoids, which have a hydroxyl group substituted at the R-3 position on the C
264 ts metabolites were compared on the basis of hydroxyl group substitution and amine ionization to eluc
265 I, and H2BDI possessing both para- and ortho-hydroxyl groups such that the inherent rotational motion
266 ross-linked polymer multilayers that present hydroxyl groups suitable for conventional phosphoramidit
267 -diene-3,20-dion e), do not have the 17alpha-hydroxyl group that characterizes dexamethasone (Dex; 9a
268 he oxidation of molecules and formation of a hydroxyl group that serves as a proton donator.
269 on that provides an array of surface-exposed hydroxyl groups that bind to polyQ peptides and may disr
270 , consists of negatively charged carboxyl or hydroxyl groups that limit attractive forces with the ce
271 ctron-deficient alkynes or alkynes with free hydroxyl groups, the coordination of alkynes is stronger
272 n a manner that buries the cholesterol 3beta-hydroxyl group; they also bind tightly to NPC1 and NPC2
273 ll electrophilic reagents that react with 2'-hydroxyl groups to interrogate RNA structure at single-n
274 cess involving nucleophilic addition of free hydroxyl groups to the carbamate linkages and exhibits a
275 ation reactions mainly involved oxidation of hydroxyl groups to the corresponding carboxylic acids.
276 he intramolecular nucleophilic attack of the hydroxyl group took place on the alkyne moiety in a high
277 ceptors through hydrogen bonding with B(OH)2 hydroxyl groups toward Cl(-), Br(-), HSO4(-), and AcO(-)
278      Vitamin D3 metabolites lacking a 1alpha-hydroxyl group (vitamin D3, 25-hydroxyvitamin D3, and 24
279 opyrimidinone bearing either a fluorine or a hydroxyl group was accomplished.
280              To test this hypothesis, the C3-hydroxyl group was synthetically deleted, and the result
281  framework bearing pendent proton-responsive hydroxyl groups was prepared and metalated with Ru(II) a
282 er the in situ formed ammonium moiety or the hydroxyl group, was observed.
283 ituted propargyl diols possessing a tertiary hydroxyl group were synthesized in a single-pot operatio
284                        The directions of the hydroxyl groups were determined on the basis of NOEs, an
285  the graphene oxide were destroyed, and more hydroxyl groups were generated, transforming the graphen
286            In addition, carbonyl, amino, and hydroxyl groups were identified as the main functional g
287                                              Hydroxyl groups were incorporated to modulate protein bi
288                                         Free hydroxyl groups were subsequently silylated in-port.
289 A-1(O2') starts attacking the phosphate as a hydroxyl group, which is hydrogen-bonded to deprotonated
290 fected the rates of biotransformation of the hydroxyl groups, which in some cases resulted in greater
291 ess copper, charge compensated by systematic hydroxyl groups, which leads to an open microporous fram
292 logous ester 27 allowed to introduce the C13 hydroxyl group with a high stereoselectivity in the hali
293                I2(II) is 4.565(2) A from the hydroxyl group with an occupancy of 0.208.
294 adium catalyzed arylation meta to the phenol hydroxyl group with iodoarenes.
295          As these monolayers expose to water hydroxyl groups with an order that resembles the one in
296 at catalyze the triphosphorylation of RNA 5'-hydroxyl groups with trimetaphosphate.
297 ole-scavenging by surface water molecules or hydroxyl groups, with associated radical formation.
298 actions are possible when there are phenolic hydroxyl groups within substrates that contain a second
299 -selective phosphorylation of three distinct hydroxyl groups within the complex glycopeptide antibiot
300 ction between adsorbed CH4 molecules and the hydroxyl groups within the pore of a material.

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