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1 iynes with isocyanates, isothiocyanates, and carbon disulfide.
2 n to electrocatalytically reduce protons and carbon disulfide.
3 o catalyze the reaction between epoxides and carbon disulfide.
4  membranes were treated with formaldehyde or carbon disulfide.
5 hase ultraviolet irradiation of a precursor, carbon disulfide.
6 I) were: carbonyl sulfide, dimethyl sulfide, carbon disulfide, 2-methylthiophene, 3-methylthiophene,
7                                              Carbon disulfide, a potentially therapeutic small molecu
8 dendrons were found to be readily soluble in carbon disulfide, a solvent of high polarizability.
9 alkyl-substituted isothiocyanates instead of carbon disulfide afforded the corresponding trifluoromet
10 by lithium diisopropylamide and reacted with carbon disulfide and methyl iodide to afford a dihydroth
11 h neutral reagents including carbon dioxide, carbon disulfide, and nitric oxide.
12 n, the fumigant mixture carbon-tetrachloride/carbon disulfide, and the fungicide chlorothalonil, resp
13 In contrast, phenylnitrene anion reacts with carbon disulfide by C+ or CS+ abstraction, forming S- or
14 , and related thiocarbonyl compounds such as carbon disulfide, certain substituted thiourea derivativ
15 e (H2S), methanethiol, dimethyl sulfide, and carbon disulfide concentrations.
16 V)O vibrates at a frequency of 986 cm(-1) in carbon disulfide, consistent with a triply bonded Cr(V)[
17 carbonyl sulfide (OCS), dimethylsulfide, and carbon disulfide (CS(2)) in the breath of a group of cys
18 quenching of nitrogenase during reduction of carbon disulfide (CS(2)) was previously shown to result
19 ghly sensitive to the volatile semiochemical carbon disulfide (CS(2)), a component of rodent breath a
20 ented here has the goal of examining whether carbon disulfide (CS2) may play a role as an endogenousl
21 ) coating was used for trimethylamine (TMA), carbon disulfide (CS2), dimethylsulfide (DMS), and dimet
22 mental and theoretical study of core-ionized carbon disulfide (CS2), we demonstrate that it is possib
23                       Irradiation of gaseous carbon disulfide [CS2(g)] at 313 nanometers produces a d
24       In this study, the release of acetone, carbon disulfide, dimethyl sulfide, nitromethane, pentan
25 oic, pentanoic acids, benzaldehyde, ethanal, carbon disulfide, dimethyldisulfide, acetone, 2-butanone
26                                              Carbon disulfide exposure leads to an identical axonopat
27  spectrometry to investigate the dynamics in carbon disulfide following the interaction with an inten
28  transformations of organic compounds (e.g., carbon disulfide, halogenated organic compounds).
29 ion of an unprecedented decameric capsule in carbon disulfide, held together by the combination of do
30 nsation of dioctylamine or didecylamine with carbon disulfide in anhydrous ethanol and compared to al
31 prepared by reaction of alcohols/thiols with carbon disulfide in the presence of bases.
32 by reaction of primary/secondary amines with carbon disulfide in the presence of bases.
33                                              Carbon disulfide is a suitable solvent for these reactio
34       Typical examples of substrates include carbon disulfide, methyl dithioacetate, methyl dithioben
35 adiation (Hg--Xe arc source) of liquid-phase carbon disulfide produces a new carbon--sulfur polymer w
36  this compound with either carbon dioxide or carbon disulfide results in insertion into the uranium-c
37         In this study we demonstrate that in carbon disulfide the chiral decameric cavity aggregate c
38 uperconducting phase observed in diamagnetic carbon disulfide under high pressure.
39 nced four-wave mixing in dilute solutions of carbon disulfide using an ultrafast (< or = 1 ps) laser

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