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1 on accompanied by spontaneous elimination of hydrogen fluoride.
2 2',3'-dideoxy nucleosides, by elimination of hydrogen fluoride.
3 spar, bypassing the necessity to manufacture hydrogen fluoride.
4  a procedure that generates highly dangerous hydrogen fluoride(1-5).
5                 Femtomolar concentrations of hydrogen fluoride, a decomposition component of nerve ag
6 ucer of fluorspar (CaF(2)), the precursor to hydrogen fluoride and fluorine, has embarked on an indus
7 to cesium hexafluosilicate by dissolution in hydrogen fluoride and the addition of cesium chloride.
8 rgeted PFAS and suspect screening as well as hydrogen fluoride and total fluorine.
9 donor and proton acceptor of hydrogen-bonded hydrogen fluoride binary complexes is investigated.
10 reement with NMR data, suggest a cyclic poly(hydrogen fluoride) bridged structure for DMEPHF.
11 ted using liquid as well as solid onium poly(hydrogen fluoride) catalysts.
12 ntitative basis for numerical simulations of hydrogen fluoride chemical lasers.
13                   Polymeric solid amine:poly(hydrogen fluoride) complexes are excellent solid HF equi
14 al calculations of stable dialkyl ether/poly(hydrogen fluoride) complexes are reported.
15                              The liquid poly(hydrogen fluoride) complexes of amines are typical ionic
16 y chemically synthesized (AO)7 and anhydrous hydrogen fluoride-deglycosylated d(AO)51.
17                          Dimethyl ether/poly(hydrogen fluoride) (DMEPHF), are stable complexes of par
18 was released from the cell wall with aqueous hydrogen fluoride (HF) and purified by gel filtration ch
19                                              Hydrogen fluoride (HF) and selected nonbasic and weakly
20  grade fluorspar (AGF) into highly hazardous hydrogen fluoride (HF) followed by neutralization with a
21                                              Hydrogen fluoride (HF) is a versatile reagent for materi
22                   In this process, anhydrous hydrogen fluoride (HF) is used to remove the side chain
23 gel treatment of the separated proteins with hydrogen fluoride (HF).
24 s anthracis vegetative cell walls by aqueous hydrogen fluoride (HF).
25 ical fluorinating reagents-are prepared from hydrogen fluoride (HF).
26 MCs and exposed to varying concentrations of hydrogen fluoride in humid air.
27               We report the encapsulation of hydrogen fluoride inside C60 using molecular surgery to
28 show increased availability of antigen after hydrogen fluoride or cellulase treatment and decreased a
29 ilable reagents (m-chloroperbenzoic acid and hydrogen fluoride pyridine) and a simple chiral aryl iod
30 cent stain and chemical dephosphorylation by hydrogen fluoride-pyridine enabled us to identify differ
31                Homologous dialkyl ether/poly(hydrogen fluoride) (R(2)O/[HF](n,), R = Et, nPr) systems
32                       The dangerous chemical hydrogen fluoride sits at the apex of the fluorochemical
33                     Treatment with potassium hydrogen fluoride smoothly converted these to the corres
34 Application of other strong acids, including hydrogen fluoride, thioacetic acid, trifluoromethanesulf
35                                              Hydrogen fluoride treatment of 89I LOS to remove phospha
36 with that of the LOS after O-deacylation and hydrogen fluoride treatment.
37 captoethyl auxiliary was stable to anhydrous hydrogen fluoride used to cleave and deprotect peptides
38             The approach is applied to model hydrogen fluoride, which in experiments exhibits unusual
39 and effectively suppresses the generation of hydrogen fluoride, which will markedly facilitate the ba
40 ormed amide bond by treatment with anhydrous hydrogen fluoride, yielding a full-length unmodified pol
41                   The high efficiency of the hydrogen fluoride zipping makes our approach attractive