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1  intramolecular loss of dinitrogen upon mild thermolysis.
2 t afford carbon-fluorine bond formation upon thermolysis.
3 tride materials that are formed via triazine thermolysis.
4  basis of spectroscopic characterization and thermolysis.
5 amolecular aggregates and microwave-assisted thermolysis.
6 that 1-butene and n-butane are formed during thermolysis.
7 ely, for the aza-Wittig reaction followed by thermolysis.
8 tigated after processing, in comparison with thermolysis.
9 itions of matrix photolysis and flash vacuum thermolysis.
10 ]octan-8-ylidene (3) by either photolysis or thermolysis.
11 hanisms of the oxidations and the subsequent thermolysis.
12 to packing in the crystalline phase prior to thermolysis.
13 undergo high yielding Ar-CF(3) coupling upon thermolysis.
14 The quinolone intermediates were prepared by thermolysis (220-240 degrees C) of anilinomethylene deri
15                                              Thermolysis (60 degrees C, 16 h) of 1 in py gave ((t)Bu3
16 dation of 29 to the sulfoxide and subsequent thermolysis afforded the hexenulose 30.
17                                              Thermolysis and photolysis experiments suggest that the
18 iazolyl cation (1) has been attempted by the thermolysis and photolysis of 1-(1,2,4-triazol-4-yl)-2,4
19      Furthermore, the products obtained from thermolysis and the kinetics of the thermolysis are inve
20 t precursor pretreatments in the solventless thermolysis approach, respectively.
21 ned from thermolysis and the kinetics of the thermolysis are investigated.
22                       Mechanistic studies of thermolysis at 122 degrees C reveal a dramatic reactivit
23 a6,eta5-bis(indenyl)zirconium THF compounds, thermolysis at 85 degrees C also resulted in C-O bond cl
24 based methods, many that involve solid-state thermolysis at or above 500 degrees C.
25 lso afford allenyl ketones upon flash vacuum thermolysis, but in addition, 3-ethynylcoumarins 6 are f
26  free amino acids were similar after HPH and thermolysis, but the former gave a more interesting vola
27                                Following the thermolysis by NMR spectroscopy indicated that only a mi
28                              Under microwave/thermolysis, carboxylic acids can couple with isonitrile
29 DPC, because it is not observed at all under thermolysis conditions, where only S1 and T0 are populat
30 omerization is reversible under flash vacuum thermolysis conditions.
31 in the production of silica nanoparticles by thermolysis, due to their structural similarities with s
32                                              Thermolysis experiments have also been conducted on a mo
33 nerally match those observed in flash vacuum thermolysis experiments.
34  in the "reverse sense" addition, which upon thermolysis forms the metal aryl complex (L)(2)Sc(C(6)F(
35                                 Flash vacuum thermolysis (FVT) of 1-methyl-5-phenyltetrazole (5b), 2-
36                                 Flash vacuum thermolysis (FVT) of 3-methylidenefuran-2(3H)-ones 3 cau
37                    In contrast, flash vacuum thermolysis (FVT) of diazoamides 1a-d, in which reaction
38                                 Flash vacuum thermolysis (FVT) of phenyl azide 29 as well as precurso
39 2, the nitrene was generated by flash vacuum thermolysis (FVT) of phenylazide and subsequently isolat
40 enone (1) has been generated by flash vacuum thermolysis (FVT) with Ar-matrix isolation of methyl sal
41 nzannulated enyne-carbodiimides 25, which on thermolysis gave the isoquinolino[2',1':1,2]pyrimido[4,5
42 icularly stable trialkylhydroxylamine, whose thermolysis half-life is 2.1 h at 150 degrees C.
43                                         Upon thermolysis, HC(SiHMe(2))(3) is formed.
44          Kinetic investigations of (i)Pr2NPA thermolysis in 1,3-cyclohexadiene and/or benzene-d6 are
45  facile 1,5-hydrogen transposition upon mild thermolysis in benzene or toluene solution (80-110 degre
46 F(5))(3)]][B(C(6)F(5))(4)] (29) also undergo thermolysis in benzene to produce their respective pheny
47 )(mu-H)2W(NSi(t)Bu3)py2 (5-py2, 5%), whereas thermolysis in DME produced ((t)Bu3SiN)2WCl(OMe) (7, 30%
48 at the rate-determining step of nitrosoamide thermolysis is made, and a mechanistic framework is prop
49                                              Thermolysis is shown to affect C-N bond scission while r
50 t likely by a concerted mechanism, while the thermolysis is well explained by the formation of radica
51  observed forming ureate ligands, which upon thermolysis isomerize to bridging carbodiimides.
52                                          The thermolysis kinetics of this vicinal trisazoalkane were
53 trast, the c,c-C(70)O(3) isomer, which has a thermolysis lifetime of 650 min at 296 K, decays thermal
54 ectrochemical, hydrothermal, and solventless thermolysis methods in order to compare their common opt
55    These microcrystals have been obtained by thermolysis of (AuCl4)(-) stabilized with tetraoctylammo
56                                              Thermolysis of (eta(5)-Me(5)C(5))(2)LaCH(TMS)(2) in cycl
57 could be synthesized (70% isolated yield) by thermolysis of (i)Pr(2)NPA in 1,3-cyclohexadiene.
58       In the absence of a hydrogen acceptor, thermolysis of (PNP)IrH2 in t-butyl methyl ether under a
59                             HCP generated by thermolysis of 1 has been observed by molecular beam mas
60                                              Thermolysis of 1 in the presence of H2C=CH(t)Bu and PhC
61 thylpyridinium tetrafluoroborate (2) and the thermolysis of 1- and 4-diazonium-1,2,4-triazoles, using
62    Inspection of the methane byproducts from thermolysis of 13, 14, 15, 25, and 29 in benzene-d(6) sh
63                                              Thermolysis of 15 under refluxing p-xylene furnished the
64                                     Extended thermolysis of 17 and 18 results in an aryl coupling pro
65                                              Thermolysis of 1a in C(6)D(6) at 45-55 degrees C leads t
66                                              Thermolysis of 1b at ~100 degrees C leads to the expulsi
67                                              Thermolysis of 2 gave mostly 1,2,4-triazole, together wi
68                                In this work, thermolysis of 2 in an attempt to favor a monomeric kety
69 m of the formation of carbon nitrides during thermolysis of 2,4,6-triazidopyrimidine.
70                                              Thermolysis of 3 in C6D6 at 95 degrees C over 48 h gener
71                               Interestingly, thermolysis of 37f bearing a 2-(methoxymethyl)phenyl sub
72                                              Thermolysis of 3a-g in the presence of zinc bromide indu
73    Compound 7 was independently produced via thermolysis of 4-py and DME (-MeOEt, -py), and THF and e
74                                              Thermolysis of 6-Me ultimately gives (PCP)Ir(CH3)(kappa(
75                                              Thermolysis of 7 at 50 degrees C formed carbocycles 6 in
76                                 In addition, thermolysis of [TCT](2)(2-) yields [TCBT]*-.
77                                              Thermolysis of a 2'-[(16)O]-O-benzoyl-[(17)O]-5'-O-(tert
78 hologies were synthesized by the solventless thermolysis of a copper alkylthiolate molecular precurso
79  formation of an acylketene generated by the thermolysis of a m-dioxolenone.
80 following bromide abstraction and subsequent thermolysis of a Pt(IV) complex bearing both Csp(3)- and
81 and composition are synthesized by efficient thermolysis of a single source precursor of mixed metal-
82                             Here we show the thermolysis of a single-source precursor (1,3-(BBr2)2C6H
83 eters wide were synthesized by a solventless thermolysis of a single-source precursor in the presence
84 colloidal nanocrystals have been prepared by thermolysis of a stoichiometric Co(2+)Fe(2)(3+)-oleate c
85 20:4omega6) or peroxyl radicals generated by thermolysis of ABIP in the presence of oxygen.
86 lenes are obtained from the high temperature thermolysis of alkanes.
87           Diradical intermediates, formed by thermolysis of alkynylcyclobutenones, can display radica
88 onditions (solution versus solid-state), the thermolysis of azide precursors yielded bridging phosphi
89                       Reinvestigation of the thermolysis of azido-meta-hemipinate (I) yielded, in add
90 mounts of 1-phenyl-1-buten-3-ynes from flash thermolysis of azulene has an activation energy of 360 k
91                                              Thermolysis of benzannulated enyne-isocyanates 13 and en
92                                          The thermolysis of bicyclo[3.2.0]hept-6-ene via a conrotator
93                The lowest-energy pathway for thermolysis of both structures proceeds through the (E,Z
94 sive CQDs can be prepared by straightforward thermolysis of citric acid in a simple one-pot, multigra
95                                              Thermolysis of compounds 2-4 in the solid-state results
96                            It was shown that thermolysis of CPs follows first-order kinetics.
97                                 In contrast, thermolysis of dicobalthexacarbonyl-complexed enynes und
98                                              Thermolysis of each of the diazonium salts in the presen
99                                          The thermolysis of furan-2-carbonyl azide results in a Curti
100                                   Subsequent thermolysis of imidazoles 14 in diphenyl ether affords 2
101                                              Thermolysis of isonitriles with carboxylic acids provide
102         Chemically inert F2PhEtyCbl resisted thermolysis of its Co-C bond at 100 degrees C, was stabl
103  elimination of methane occurs upon solution thermolysis of kappa(3)-Tp(Me)2Pt(IV)(CH(3))(2)H (1, Tp(
104                                         Mild thermolysis of Lewis base stabilized phosphinoborane mon
105 yrolysis" (FFP) technique was applied to the thermolysis of Meldrum's acid derivatives, pyrrole-2,3-d
106 on polyethylene processing temperatures, the thermolysis of Meldrum's acid to ketene provides the des
107 nitrido complexes have been prepared via the thermolysis of metastable vanadium(III)-azido precursors
108          This is the result of the very fast thermolysis of MPAN at high temperatures that affects th
109                                 Furthermore, thermolysis of N-(4-chloro-5H-1,2,3-dithiazol-5-ylidene)
110 d core was formed stereoselectivity from the thermolysis of N-[(2-methyl-2-cyclopentenyl)methyl]-N-(4
111                                     Extended thermolysis of neutral [Ph(2)BP(2)]Pt(Ph)(THF) (16) resu
112  absence of metals have been achieved by the thermolysis of nonconjugated 2-azetidinone-tethered bis(
113 old NP core (PS-AuCoNPs) were synthesized by thermolysis of octacarbonyldicobalt [Co(2)(CO)(8)] in th
114 esis of non-PGM ORR electrocatalysts through thermolysis of one-pot synthesized ZIF is demonstrated.
115 es include organic solution-phase synthesis, thermolysis of organometallic precursors, sol-gel proces
116                           In contrast to the thermolysis of p-benzoquinone, which does not decompose
117  thermodynamic activation parameters for the thermolysis of P2A2 in a solution containing different a
118 in approximately 50% yield by the short-time thermolysis of Pd10(CO)12{P(p-Tolyl)3}6 in THF solution
119 re exposed to hydroxyl radicals generated by thermolysis of persulfate under basic pH conditions and
120                                              Thermolysis of phosphorus-based vinyl azides under solve
121 ed nine exposure units of smoke generated by thermolysis of pine woodchips (80 g).
122                                          The thermolysis of polyfused cyclobutanes with a cis,syn,cis
123                                              Thermolysis of RPA benzene-d(6) solutions leads to anthr
124 ents and thermal gravimetric analysis of the thermolysis of Ru(2)(D(3,5-Cl(2))PhF)(4)N(3), and by Arr
125 s absorb light, get heated, and induce focal thermolysis of sebaceous glands.
126 olecular beam mass spectrometry study on the thermolysis of solid P2A2 reveals the direct detection o
127                                              Thermolysis of spiro[2.4]hepta-1,4,6-triene (1a) at 50 d
128   The pyrazino derivative 1c was formed upon thermolysis of sulfoxide 14c obtained from 2c.
129                            Mild flash vacuum thermolysis of tetrazolo[1,5-b]pyridazines 8T generates
130                                              Thermolysis of the arylpalladium cyanoalkyl complexes le
131                                              Thermolysis of the complex results in N-O bond homolysis
132                                              Thermolysis of the crude peroxoniobium compounds (72-96
133                                   Controlled thermolysis of the deposited alkoxide gives the metal a
134                                              Thermolysis of the enyne-carbodiimide 42 having a methox
135 edirect the reaction toward 32 by conducting thermolysis of the enyne-carbodiimide 7e in the presence
136                                              Thermolysis of the enyne-carbodiimides 7 having the cent
137                                              Thermolysis of the heterobimetallic phosphinidene comple
138 ehyde, which is easily generated as a gas by thermolysis of the inexpensive and abundant paraformalde
139                                              Thermolysis of the iron(IV) nitride complex [PhB(tBuIm)3
140                                              Thermolysis of the latter mixture afforded ((t)Bu3SiNH)(
141                                        While thermolysis of the macrobicyclic triene lactone 12 did n
142                                              Thermolysis of the methyl and hydride derivatives, ((tBu
143                                              Thermolysis of the methyl-borylamide (NacNac(NMe2))Sc(Me
144                                              Thermolysis of the Pd chelates results in beta-acetate e
145            Mass spectrometry and solid state thermolysis of the precursors generated common fragments
146                                              Thermolysis of the pyrazolo[3,4-e][1,2,4]dithiazines 7 g
147 ido[4',3':4,5]pyrrolo[2,3-b]quinolines 8 via thermolysis of the pyridannulated enyne-carbodiimides 14
148                                              Thermolysis of the Rh(III)-Me complex (DPEphos)RhMeI2 (1
149                                              Thermolysis of the ring-opened product ICF(2)CF(2)CFIOR(
150                                              Thermolysis of the silver complexes in the presence of C
151                                              Thermolysis of the terminal azido Ru(2)(D(3,5-Cl(2))PhF)
152                                              Thermolysis of the titanocene TEMPO complexes in the pre
153 d 8-MeOAdo(*) radicals are generated by Co-C thermolysis of their respective precursors, AdoCbl and 8
154                                 Flash vacuum thermolysis of these adducts leads to various isotopic i
155                                              Thermolysis of these complexes in the presence of PPh(3)
156                                              Thermolysis of these furans resulted in an intramolecula
157                                              Thermolysis of these furans resulted in an intramolecula
158                                              Thermolysis of this complex at 80 degrees C resulted in
159                                              Thermolysis of this complex promotes extrusion of azoben
160                         Product studies upon thermolysis of this precursor give the same products as
161     Ammonia (NH(3)) is produced in situ from thermolysis of urea and hydrolysis of isocyanic acid (HN
162                                              Thermolysis of {[PhBP(CH(2))(Cy)(3)]Fe}(2)(mu-eta(1):eta
163 photolysis and two possible pathways for the thermolysis, one involving proton transfer from the OOH
164 ylamine derivatives in aromatic solvents via thermolysis or acid-catalyzed decomposition may not be c
165              The Boc group can be removed on thermolysis or left intact during subsequent transformat
166 (mu2 -CH2 )] (2) can be cleanly prepared via thermolysis or photolysis of [(Ar'O)2 Nb(CH3 )2 Cl] (1)
167             These ozonides lose O(2) through thermolysis or photolysis to form various isomers of C(7
168 es (N-ethoxycarbonyl)carbamoyl chloride upon thermolysis, or (N-ethoxycarbonyl)isocyanate upon treatm
169                             Slow, protracted thermolysis produces a fractionation line of shallower s
170                                          The thermolysis product readily reverts to active catalysts
171                                          The thermolysis products obtained by refluxing a series of v
172  the 26-mer), but a significant abundance of thermolysis products were also observed.
173 s and strong vertical mixing the slower MPAN thermolysis rate aloft could increase the fraction of MP
174                 THF inhibits the rate of the thermolysis reaction in all three cases.
175 l ether from 2,2-dimethoxypropane during the thermolysis reaction.
176 s carbon nitride networks formed by triazine thermolysis reactions.
177 ement of the thiophene ylide, in contrast to thermolysis results.
178 r [2 + 2] photocyclization is present in the thermolysis step, however, the result of a formally "sym
179                       The microwave-assisted thermolysis strategy is simple, rapid, and robust, there
180 nd indicate the utility of gas-phase NMR for thermolysis studies of a variety of materials that relea
181    In their denuded state produced by gentle thermolysis, the cluster carbonylates yield nanoparticle
182                                         Upon thermolysis, these compounds give YbSe(x)().
183 itive C-N and C-C reductive elimination upon thermolysis to form N-methylsulfonamides and ethane, res
184                                      Because thermolysis to form seven stable products proceeds stepw
185 er, by using multiphoton infrared photolysis/thermolysis to initiate decarbonylation, it was shown th
186 S5 nanosheets that are formed by solventless thermolysis, utilizing Cu alkanethiolates as single-sour
187 rathiomolybdate ((NH4)2MoS4), and subsequent thermolysis was used to produce large area MoS2 layers.
188  that the polymer decomposes to monomer upon thermolysis, which indicates that the polymerization-dep
189 f diatomic oxygen to IPU and is subjected to thermolysis whose rate depends on temperature, pH, the p
190 The a,b-C(70)O(3) isomer dissociates through thermolysis with a decay time of 14 min at 296 K to form

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