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1 olic NH moiety with a meso-sp(3) -hybridized carbon atom.
2  out-of-plane ppi occupancies of the central carbon atom.
3 arkably short Pd-Cu bond and a trigonal ipso carbon atom.
4 ach have bonds to three sulfur atoms and one carbon atom.
5 associated with pyramidalization around this carbon atom.
6 hat accumulate positive charge at the acetal carbon atom.
7 m stabilization of the electron-deficient C1 carbon atom.
8 of O2(*-) and Ph(*) addition to the nitronyl carbon atom.
9 -catalyzed monohydroxylation of the benzylic carbon atom.
10 a-nitroamines possessing a fully substituted carbon atom.
11 h an unconventional strategy for replacing a carbon atom.
12 nnected via the N-atom to the former carbene carbon atom.
13 egardless of the chirality at the asymmetric carbon atom.
14 ttern opposite T but with N3 replaced with a carbon atom.
15 yl ring and the adjacent hydroxy-substituted carbon atom.
16 roved most effective in installing the final carbon atom.
17 n comparison, the cyano radical adds via its carbon atom.
18 ic acid groups precisely every 21st backbone carbon atom.
19 ly leading to derivatization of the internal carbon atom.
20 t of d --> p backbonding from gold to the C1 carbon atom.
21 dispersed and surrounded by sp(3)-hybridized carbon atoms.
22 bearing functionality at one of the tertiary carbon atoms.
23 reactive aliphatic or electron-rich aromatic carbon atoms.
24 roduced by a condensing enzyme from 28 to 30 carbon atoms.
25  A vs. 2.783(2) A] between the ipso and para carbon atoms.
26  C-C bonds between adjacent sp(2)-hybridized carbon atoms.
27 s for a dimerization are always the terminal carbon atoms.
28 "fullerene-type chemistry" at their interior carbon atoms.
29 om a mixture of sp(2)- and sp(3)-coordinated carbon atoms.
30  is consistent with a fatty acid of about 10 carbon atoms.
31 ely large organic molecules containing 15-20 carbon atoms.
32 th unique eta(5) interactions involving meso-carbon atoms.
33 voring the ring carbon atoms over the linear carbon atoms.
34 lic olefins having ring sizes exceeding five carbon atoms.
35 1)-hydroxylated fatty acids comprising 26-34 carbon atoms.
36 e small optical absorption of a monolayer of carbon atoms.
37 red electron is delocalized over two carbene carbon atoms.
38 cally contain fatty acids (FAs) of 16 and 18 carbon atoms.
39 between two sterically encumbered quaternary carbon atoms.
40 eridine rings with adjacent tetrasubstituted carbon atoms.
41 alkyl chain of the bolaform has more than 14 carbon atoms.
42 yl-beta-hydroxy fatty acids comprising 60-90 carbon atoms.
43 gle bond rotation or through the loss of two carbon atoms.
44 ospholipids with hydrocarbon chains of 18-22 carbon atoms.
45  building blocks for bond formation to sp(3) carbon atoms.
46 ers with the carbon chain containing 2 to 10 carbon atoms.
47 ert alcohols into aldehydes elongated by two carbon atoms.
48 nked by an ethylene bridge between the alpha-carbon atoms.
49 to the bonding configuration of near-surface carbon atoms.
50 ies are extremely sensitive to the number of carbon atoms.
51 o sp(2) rehybridization of one of the alkyne carbon atoms.
52 g two different molecule lengths of 6 and 11 carbon atoms.
53 g constants, Aiso((13)C), for the individual carbon atoms.
54 construct C-C bonds between sp(3)-hybridized carbon atoms.
55 nd olefin migration can be sustained over 30 carbon atoms.
56 s of QMs produced following ESPT to aromatic carbon atoms: (1) reverse proton transfer (RPT) to regen
57 e ring are, the (1) coplanarity of the three carbon atoms, (2) relatively shorter (1.51 A) C-C bonds,
58  catecholamide units was increased from four carbon atoms (4-LICAM(4-)) to five, six and eight (5-, 6
59 re is an allylic substituent on the benzylic carbon atom, a chemoselective switch was observed, which
60 ction of a bond between two sp(3)-hybridized carbon atoms, a fundamental unit of organic chemistry, r
61 n a SAM to calculate the surface coverage of carbon atoms after each stepwise addition.
62                 The properties of individual carbon atoms allow them to chain into complex molecules
63 en-rich triazole features a highly polarized carbon atom allowing the complexation of anions by hydro
64 ally a nucleophilic substitution at an sp(2) carbon atom, allows the direct regioselective incorporat
65 roup that possesses a tertiary or quaternary carbon atom alpha to the carbon-zirconium bond can not b
66 planarization of the central tetracoordinate carbon atom and demonstrates the influence of bridgehead
67 h a partial double bond between each carbene carbon atom and silicon atom.
68 onolayer of alkanethiols with a length of 11 carbon atoms and a carboxyl terminal group can efficient
69                EWR images reveal that single carbon atoms and carbon-fluorine pairs in C2F chair alte
70 lipid species were weighted by the number of carbon atoms and double bonds, the strongest inverse ass
71 ng the electronic structures of the adjacent carbon atoms and facilitates the adsorption of OER inter
72 wo or more contiguous stereogenic quaternary carbon atoms and key reactions in their total or partial
73 e between the electrophilic and nucleophilic carbon atoms and the structure of the phosphorus moiety.
74                PUFAs, containing at least 18 carbon atoms and three unsaturated bonds, activate TRPA1
75 ts that build up to form chains and rings of carbon atoms and ultimately form those well-known isolat
76           For example, whilst oxidized sp(3) carbon atoms and vacancies in a graphene sheet can degra
77    Most of these organic compounds retain 10 carbon atoms, and some of them are remarkably highly oxi
78 ations influence the phonon bands of bonding carbon atoms, and the discrepancies of phonon bands betw
79 ally stable, unless bonds to the stereogenic carbon atom are broken and re-formed.
80 that the bulky methyl-substituted bridgehead carbon atoms are attached to C2 and C3 of the 1,3-butadi
81 ct photoluminescence (less than 0.01% of the carbon atoms are bonded to a functional group).
82 non-soap, amphiphilic molecules in which the carbon atoms are derived from annually renewable feedsto
83 e amino acids with alpha,alpha-disubstituted carbon atoms are described, including the discovery of o
84 lpha-hydroxylated acyl-chains of at least 24 carbon atoms are enriched in secretory vesicle subdomain
85                         Single bonds between carbon atoms are inherently challenging to activate usin
86           Fragment ions containing different carbon atoms are of special interest, since they can car
87                                      The sp3-carbon atoms are photothermally converted to sp2-carbon
88 of complexes with differentially substituted carbon atoms are poorly understood.
89 nd the discrepancies of phonon bands between carbon atoms are responsible for the remarkable drops in
90 ation demonstrates that 18% of the original carbon atoms are still present in the film.
91                                The remaining carbon atoms are then installed by means of a diastereos
92                      Compounds with up to 20 carbon atoms are treated.
93 as 1.6 nm, comprising only approximately 400 carbon atoms, are capable of housing stable photolumines
94 d to the p electrons of the nearest-neighbor carbon atoms around the VSiVC divacancies.
95 phene, which is a two-dimensional crystal of carbon atoms arranged in a hexagonal lattice, has attrac
96  sp hybridization of the ACP internal alkene carbon atom as controlling the regiochemistry of the ACP
97 ion, so it does not undergo 1,2-shift of the carbon atom, as observed in the acid-catalyzed reaction.
98 d to the gold leads through an sp-hybridized carbon atom at each side.
99  established the presence of an interstitial carbon atom at the center of the iron-molybdenum cofacto
100 tom at the nucleophile moiety and a tertiary carbon atom at the electrophile moiety.
101 rs, to form products containing a quaternary carbon atom at the nucleophile moiety and a tertiary car
102 ions of acetals having benzyloxy groups four carbon atoms away can be highly diastereoselective.
103 mines with remote structural differences six carbon atoms away from the binding site.
104    During SNAr, attack of a nucleophile at a carbon atom bearing a 'leaving group' leads to a negativ
105 han the competing process of addition to the carbon atom bearing a nucleofugal group (usually a halog
106  double-trifluoromethylated sp(3)-hybridized carbon atom between the two aromatic rings and 2) the tw
107                     In Be5C2 monolayer, each carbon atom binds with five beryllium atoms in almost th
108                  Graphene, a single layer of carbon atoms bonded in a hexagonal lattice, is the thinn
109  contain all-carbon quaternary stereocentres-carbon atoms bonded to four distinct carbon substituents
110  first reported example of a five-coordinate carbon atom bound only to separate (that is, monodentate
111 ew graphitic structure formed of rings of 10 carbon atoms bridged by carbene groups yielding seven-me
112 n sp(2)-to-sp(3) hybridization change of the carbon atom bridging the chromophore cyclic moieties was
113 s of four products having the same number of carbon atoms but slightly different hydrogen numbers ran
114 f imidazolines with a fully substituted beta-carbon atom by a Mannich-type addition/cyclization react
115 a temporary functional group at the terminal carbon atom by C-H bond functionalization, followed by t
116  perfluoroalkyl group attached to a tertiary carbon atom by using an alkyl-alkyl cross-coupling.
117 nerate stable radical centers on the carbene carbon atoms by employing the so far hidden and unique a
118 itional isotopomer distribution of aspartate carbon atoms by gas chromatography/tandem mass spectrome
119 on atoms are photothermally converted to sp2-carbon atoms by pulsed laser irradiation.
120 t semi-quantitative estimate of the oxidized carbon atoms by silver-based nanoparticles is achieved.
121 ween the methyl hydrogen atoms and the ortho carbon atom C(o) well below the van der Waals distance o
122 ich the stereogenic center was positioned at carbon atom C2.
123 Br < CN < COOMe < PO(OEt)(2)], attack at the carbon atom C4 prevails, delivering the respective trans
124 that the combination of two unusual forms of carbon atoms can lead to unexpected chemical behavior, a
125  energy of the p(pi) orbital at the divalent carbon atom compared to normal sp(2) carbon.
126 eads to nucleophile trapping at the benzylic carbon atom connected to the aryl substituent.
127 fects of organic substituents at the carbene carbon atom coordinated to the gold atom are evaluated f
128 forward methodology for the synthesis of six-carbon atom d- and l-arabino-hex-2-ulosonic acids.
129                       Based on the number of carbon atoms, dialkylamines showed a considerably lower
130 a BF(4)(-) ion (an S(N)2-type process at the carbon atom distal to the ammonium moiety).
131                         This addition of two carbon atoms doubles the quantum efficiency and improves
132 anic C-Se-C compounds (i.e. Se bonded to two carbon atoms, e.g. methylselenocysteine).
133 the hydroisomerization of alkanes with 18-30 carbon atoms encountered in petroleum refining.
134 sphorus substituent from the nitrogen to the carbon atom followed a retentive course with some racemi
135  ring, respectively, thus exposing different carbon atoms for the attack by O2.
136                                 In contrast, carbon atoms from starch, a polymer of glucose, were inc
137 s separated by two or three sp(3)-hybridized carbon atoms from the actual chromophore, solvation effe
138 (f(MF)) and the fraction of sp(3)-hybridized carbon atoms (Fsp(3)).
139 o occur, while substitution at the exocyclic carbon atom has an impact on the reaction pathway and en
140 t of different substituents at the saturated carbon atom has not been systematically examined.
141 eaction requiring activation of an aliphatic carbon atom, has remained enigmatic.
142 hene, a two-dimensional honeycomb lattice of carbon atoms, has been attracting much interest in recen
143                             Only half of its carbon atoms have an attached hydrogen, which presented
144 of O-doped benzorylenes, in which peripheral carbon atoms have been replaced by oxygen atoms, has bee
145 is- or trans-position of the terminal alkene carbon atom (hex-4-enyl and hex-4-enoyl substitution), t
146 ontained minor fatty acids with more than 20 carbon atoms, higher hydrocarbons and phytosterols.
147 r both highly unsaturated fatty acids (>/=20 carbon atoms) (HUFAs) and polyunsaturated fatty acids (>
148 ssing numerous contiguous, fully substituted carbon atoms (i.e., tertiary alcohols and quaternary cen
149 rmed the largest negative charge for the C12 carbon atom in antipodal position, in agreement with the
150 of pretreated barley straw adsorbent and pi* carbon atom in benzene ring attached to fluorine of levo
151 d by abstraction of a hydrogen atom from the carbon atom in gamma-position relative to the carbonyl o
152 aturing a key formyl group and a quaternized carbon atom in good yields.
153  induce undesired epimerization of the alpha-carbon atom in polyesters resulting in the loss of isota
154 ntroducing various coupling functions on one carbon atom in the beta-N position of the macrocycle, le
155 n the imino nitrogen (pathway "a") or on the carbon atom in the C horizontal lineN moiety of aroylimi
156  (CN) with acetylene, the replacement of the carbon atom in the cyano group by an isovalent silicon a
157  deuterated methyl groups at the distal (C3) carbon atom in the double bond under dissociative and as
158 i values were achieved by inserting an extra carbon atom in the linker connecting the N(9) atom of gu
159 ntioselective oxygen transfer from sulfur to carbon atom in the presence of chiral rhodium(II) carbox
160 d their role in creating a quaternary chiral carbon atom in this triple catalytic system.
161 aphene molecules, bearing more than 90 sp(2) carbon atoms in aromatic cores, is very challenging, whi
162                           The replacement of carbon atoms in bioactive substances with silicon is bec
163 amide species with an even and odd number of carbon atoms in both chains were detected in all ceramid
164 the molecular weight and the exact number of carbon atoms in each molecule provides extremely accurat
165 embranes of the three domains, the number of carbon atoms in eubacteria was found to be similar to th
166 etries, (ii) inexpensive 4-31G basis set for carbon atoms in fc calculations, and (iii) individual pa
167 ron sites that are coordinated to sulfur and carbon atoms in FeMoco have been proposed to be the subs
168              The high degree of reduction of carbon atoms in glycerol confers the ability to produce
169 data show exactly the opposite-the number of carbon atoms in lipids of eukaryotes was higher than in
170 ances of all isotopomers of ergosterol whose carbon atoms in the 5,7-diene moiety of the sterol skele
171 ) elucidate the isotopic affiliation between carbon atoms in the alkaloids and those in the precursor
172 rrier concentration by substituting specific carbon atoms in the hexagonal graphene lattice with p- o
173                     Increasing the number of carbon atoms in the hydrophobic chain caused an increase
174 zation of NBO hybridization coefficients for carbon atoms in the involved C-H bonds allows for a sign
175  carbon and CO components show clustering of carbon atoms in the melt at high pressures, hinting towa
176 wo or more contiguous stereogenic quaternary carbon atoms in their intricate structures are reviewed
177 (13)C-carbene) 34 carries (13)C label on all carbon atoms, including the CN carbon.
178 of n-alkanethiolates SCn (with n = number of carbon atoms) incorporated in junctions having structure
179 on shows that the reactivity of the terminal carbon atoms increases with increasing numbers of alkyne
180 cal character are formed by insertion of the carbon atom into one P-N bond.
181 ments, which showed incorporation of labeled carbon atoms into different metabolites.
182 ose to the initial value of Atz, because the carbon atoms involved in the reaction step are not prese
183 n increase in the crowdedness of the central carbon atom is explained by differences in sp(3) charact
184  of molecules contacted via an sp-hybridized carbon atom is lower than the ones using sp(3) hybridiza
185 t the photochemical reactivity of a specific carbon atom is modified as a result of the presence of t
186                           Proton transfer to carbon atoms is a significant catalytic challenge becaus
187 O25-Ice Proxy for the Southern Ocean with 25 carbon atoms-is proposed as a proxy name for diene II.
188 ger decay after X-ray photoionization of the carbon atom K shell.
189 mainly involve motion of the pseudo-anomeric carbon atom, knowledge that should stimulate the design
190                          Tethers less than 6 carbon atoms lead to 1,3-regioisomers due to conformatio
191 ofuran (THF) ring at the stereogenic central carbon atom led to a significant shift in physicochemica
192  for the selective cyanation of the carbonyl carbon atom linked to the N atom of proline residues wit
193 enyl pyridine groups attached to two methano-carbon atoms located at the trans-1 positions was design
194                                       As the carbon atoms migrate from the feedstock to catalyst to f
195 near polyethylene (<0.7 methyl-branches/1000 carbon atoms, Mn = 4.2 x 10(5) g mol(-1)).
196 odes are attached to those positions of an N-carbon atom N-electron closed-shell hydrocarbon where th
197  observed POA was characterized by number of carbon atoms (NC), number of double bond equivalents (ND
198 kanethiolates having odd and even numbers of carbon atoms (nodd and neven) using junctions with the s
199 in long-chain aliphatic aldehydes, with even carbon-atom numbers from C22 to C30.
200 mall bite angles favor attack on the central carbon atom of an allenylpalladium intermediate to affor
201      The (13)C chemical shift of the central carbon atom of carbenes in their parent and protonated f
202 ce more downfield shift, whereas the central carbon atom of carbones will experience a lesser downfie
203 attack by a nucleophilic Pd-OH moiety on the carbon atom of coordinated micro-OCS2, which on deproton
204 ing HPLC-HRMS analysis by the detection of a carbon atom of nonfungal origin.
205 synthase, AroA) is protonating the methylene carbon atom of phosphoenolpyruvate, or EPSP, in the reve
206 nosulfide radical with its boron atom to the carbon atom of the acetylene molecule, leading to the tr
207  adduct between the alphaLys352 and the beta carbon atom of the alpha,beta-unsaturated lactone.
208 s a base that abstracts a proton from the C2 carbon atom of the covalently bound subsite -1 glucosyl
209                                       If the carbon atom of the imine could be rendered electron-rich
210 ts as a nucleophile by attacking the central carbon atom of the isocyanate (interacting with the pi-s
211    This is assigned to pyramidalization at a carbon atom of the isomerizing bridging double bond.
212 olvolysis via QM9 and solvent-assisted PT to carbon atom of the naphthalene giving zwitterion.
213 g of quinoxalin-2(1H)-one becomes the fourth carbon atom of the newly formed pyrrole ring.
214                     The basicity of the ipso-carbon atom of the pincer ligand was investigated in a r
215  elementary reactions with methane where the carbon atom of the product is oxidized and has a FOS les
216 or ability of the positively charged central carbon atom of the triphenylmethyl moiety.
217 ansfer of a methyl group to an electrophilic carbon atom of tryptophan.
218  contains the chemical formulas and retained carbon atoms of a wide range of trimethylsilyl and tert-
219 rbonyl has demonstrated that the boron-bound carbon atoms of all of these reaction products arise fro
220 tion of a single bond between the C2' and C6 carbon atoms of cis-resveratrol that generates a new cen
221 onic surfactants, with increasing numbers of carbon atoms of double chain surfactant, were analyzed o
222 valent functionalization degree of 3% of the carbon atoms of graphene is reached after 3-5 h of ion e
223 hene, a two-dimensional honeycomb lattice of carbon atoms of great interest in (opto)electronics and
224 ygenase that is able to act on two different carbon atoms of its C4-aminated substrate, allowing its
225 ists of a localized strain soliton where the carbon atoms of one graphene layer shift by the carbon-c
226  charged lipid headgroups and the very first carbon atoms of the acyl chains, at the PimA-phospholipi
227 ndary amine building block that contains all carbon atoms of the D and E ring of the natural product
228  extremely close contact between the central carbon atoms of the threaded hexayne chains (C...C dista
229 ledge of the number and position of retained carbon atoms of the unfragmented molecule.
230                                The C1 and C2 carbon atoms of the vinylidene complex underwent facile
231  the atomic distance between reference alpha carbon atoms of transmembrane domains IV and V and I and
232 he lower molecular mass range (maximum of 10 carbon atoms) of these DBPs.
233 properties based purely on pi electrons from carbon atoms offer a fertile ground in the search for ex
234 he C horizontal lineC bond and at the iminic carbon atom on the chemoselectivity of the reduction was
235 age and bound in eta(2)-fashion to a pair of carbon atoms on an adjacent open cage.
236 could be functionalized by favoring the ring carbon atoms over the linear carbon atoms.
237       Defining the number of four-coordinate carbon atoms per benzene formula unit as the degree of s
238  caused an increase in the average number of carbon atoms per molecule of the HOMs, which is consiste
239 e of the FAD isoalloxazine with the anomeric carbon atom poised for nucleophilic attack by the FAD N5
240 well as atomic-resolution observation of the carbon atom positions between neighboring crystal grains
241  from the methylene (CH2OH) and methyl (CH3) carbon atom positions of the original ethanol, respectiv
242 amed 4-6 carbophene by authors, in which all carbon atoms possess sp(2) hybrid orbitals with some dis
243 we found that the efficient diffusion of the carbon atoms present at the interface between Cu and the
244 ally a nucleophilic substitution at an sp(2) carbon atom, proceeds by a concerted addition-eliminatio
245 omplex in which iron has bonds to sulfur and carbon atoms, providing a model for N2 coordination in t
246 UFAs) and polyunsaturated fatty acids (>/=18 carbon atoms) (PUFAs).
247 that led to cyclopentenones with vicinal all-carbon-atom quaternary centers (see example; SEM=2-(trim
248 mmetric centers, one tertiary and one an all-carbon-atom quaternary stereocenter, in high yield and o
249 elective asymmetric synthesis of vicinal all-carbon-atom quaternary stereocenters is a challenging pr
250             We propose that the interstitial carbon atom recently assigned in the nitrogenase cofacto
251 nits, whereas the reactivity of the internal carbon atoms remains very low independent of the number
252                                   We observe carbon atom removal from the nanopore edge in situ using
253 anotube sidewall segments with more than 200 carbon atoms represents a challenging task for tradition
254 alyl-CoA, possessing tertiary and quaternary carbon atoms, respectively, are discussed.
255 and long alkyl chains comprised of 12 and 14 carbon atoms, respectively.
256 nd Bpin are installed on the alpha- and beta-carbon atoms, respectively.
257 n low-energy pi-electrons located at relaxed carbon atom sites.
258  a molecular "sticky tape" with the last 3-4 carbon atoms sticking out into bulk solvent.
259 ns, such as methyl transfer to electrophilic carbon atoms, sulfur to Calpha atom thioether bonds, or
260 In the series of complexes 3-5, the bridging carbon atom systematically changes its hybridization fro
261 phores Cy3 and Cy5 attached to DNA via three-carbon atom tethers, showing that they stacked onto the
262 aps, akin to s-p hybridization in an organic carbon atom that is beneficial to form stable species.
263  in a chiral molecule is an sp(3)-hybridized carbon atom that is connected to four different substitu
264 milies depending on the number of contiguous carbon atoms that constitute their central framework.
265 establish a CH/pi bond with one of the ortho carbon atoms (the C(o) side), leading to a characteristi
266            In the case of a bolaform with 12 carbon atoms, the electrostatic repulsion between the ca
267 yyne, with up to 24 contiguous sp-hybridized carbon atoms, threaded through a variety of macrocycles.
268 ar spring that attracts the surrounding cage carbon atoms through strong interactions with the two mo
269 ayer below the 1st layer as the diffusion of carbon atoms through the Cu bulk after complete dehydrog
270 and iodine) are equivalently attached to two carbon atoms through three-center bonds, are well establ
271 th 1 via nucleophilic attack at the carbonyl carbon atom to give boryl-functionalized Fischer carbene
272 hanging the alkyl on phenone from a tertiary carbon atom to secondary to primary toward an unsubstitu
273  crotyl group is translocated via its distal carbon atom to the hydroxymethyl functionality.
274 somer the distance between hydrogen atom and carbon atom to which it migrates in the result of the si
275 n approximately half of these compounds, the carbon atom to which the halogen is bound is sp(3) -hybr
276 ound enabled the assignment of the number of carbon atoms to each fragment signal and allowed the gen
277 he stepwise oxidation of aldehyde and methyl carbon atoms to form a 1,2-dicarboxylate.
278              Quaternary carbon stereocentres-carbon atoms to which four distinct carbon substituents
279 n-enhanced wrinkles cause the aggregation of carbon atoms towards the inner edge and contribute to th
280 example of a four-electron reaction involves carbon atom transfer from BAC to create a cyanide ligand
281 n which gold is bound to a formally divalent carbon atom, typically formulated as gold carbenes or al
282 e, SAMs of alkylthiolates with more than ~12 carbon atoms undergo an abrupt change of orientation fro
283 ogy, in that more than half of the substrate carbon atoms undergo changes in bonding and hybridizatio
284  high yield, and the reactivity of meso-free carbon atom was demonstrated by carrying out functionali
285  saturated fatty acid chloride containing 18 carbon atoms was studied in order to obtain procyanidin
286 e group, the O atoms on the second and third carbon atoms were proved to be the most probable sites f
287 er (-C*HXR(2)) adjacent to the electrophilic carbon atom, were prepared and subjected to SN1-type sub
288  for the structural relaxation of graphene's carbon atoms when placed on a boron nitride substrate, a
289 SN2 reaction is its intolerance for tertiary carbon atoms: whereas primary and secondary alcohols are
290  hydride in 1 from the ruthenium to the meta-carbon atom, which generates 1'' with a frustrated Lewis
291 n-insensitive densities of ~18 branches/1000 carbon atoms, which are ~17 and ~3 times (conversion-dep
292 cycles containing a high proportion of sp(3)-carbon atoms, which confer precise spatial definition up
293 etic characteristic between the magnetic and carbon atoms, which leads to either ferromagnetic or ant
294                     The replacement of sp(3) carbon atom with sp(2) (C horizontal lineO) at the 8-pos
295 molecular gas-phase reaction of ground-state carbon atoms with 1,3,5-cycloheptatriene (C7 H8 ) on the
296 ) mediated fluorinations of aliphatic Csp(2)-carbon atoms with special focus on the opportunities pro
297 er goal, but complexes of highly substituted carbon atoms with transition metals are rare, and the fa
298 ate single-layer, two-dimensional network of carbon atoms with ultrasensitive sensing capabilities.
299 s activity against substrates with up to six carbon atoms, with optimal activity against propionaldeh
300 The better compound (TPP(+)C10) contained 10 carbon atoms within the linker chain and exhibited an IC

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