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1 athway involving decomposition to ketene and hydrogen cyanide.
2 cetylene, ethylene, ethane, diacetylene, and hydrogen cyanide.
3 nergy organic compounds such as cyanamide or hydrogen cyanide.
4 te to the full degradation of amygdalin into hydrogen cyanide.
5 es on UV light, inorganic sulfur species and hydrogen cyanide.
7 r agent sulfur mustard (HD), the blood agent hydrogen cyanide (AC) and the choking agent chlorine (CL
8 his process is studied here for the cases of hydrogen cyanide, acetylene, and cyanoacetylene in heliu
9 r dioxide, acrylonitrile, cyanogen chloride, hydrogen cyanide, acrolein, formaldehyde, and ethyl para
10 oxazolidine hydrolysis or ring-opening with hydrogen cyanide allowed us to synthesize N-methyl- or N
11 re equilibrium mixture of cometary material, hydrogen cyanide and acetylene were produced with yields
12 Genetic and chemical analyses identified hydrogen cyanide and cyclic lipopeptides as key speciali
14 ses are presumed to have been available from hydrogen cyanide and other nitrogenous species formed in
15 be derived by the reductive homologation of hydrogen cyanide and some of its derivatives, and thus t
16 taldehyde, hexanoic acid, hydrogen sulphide, hydrogen cyanide, and methyl phenol, were found to be si
17 ow that acrolein, formaldehyde, benzene, and hydrogen cyanide are the dominant contributors to gas-ph
20 spatial distributions of carbon dioxide and hydrogen cyanide, both considered to be products of come
21 we show that these sugars can be formed from hydrogen cyanide by ultraviolet irradiation in the prese
22 The results obtained bring evidence that hydrogen cyanide can be adsorbed onto aerosol liquid wat
23 tion by endogenous plant enzymes can release hydrogen cyanide causing potential toxicity issues for a
24 lar, the self-assembly of exclusively linear hydrogen cyanide chains is observed, even when the folde
26 )- and (E)-iminoacetonitriles (NCCH=NH), two hydrogen cyanide dimers, are described as key compounds
27 tive thermal oxidizers to reduce ammonia and hydrogen cyanide emissions; spar caps are made using VCF
28 s operates catalytically to disproportionate hydrogen cyanide, first generating the sugars and then s
29 eaction of an imine or imine equivalent with hydrogen cyanide, followed by nitrile hydrolysis-is an e
30 tissue disruption leads to release of toxic hydrogen cyanide gas, which can deter herbivore feeding.
35 ent results in prebiotic chemistry implicate hydrogen cyanide (HCN) as the source of carbon and nitro
36 rge ionization source (HiT-CD-IMS) to detect hydrogen cyanide (HCN) emitted by Pseudomonas aeruginosa
37 ch as ammonia (NH(3)), aldehydes (RCHO), and hydrogen cyanide (HCN) has been recognized as a viable r
38 e inferred deuterium/hydrogen (D/H) ratio in hydrogen cyanide (HCN) is (D/H)HCN = (2.3 +/- 0.4) x 10(
44 en or chlorine (and other halogens) can form hydrogen cyanide (HCN) or hydrogen chloride (HCl) and th
50 odium cyanide in aqueous solution at pH 7.4, hydrogen cyanide (HCN) was found to degas from the solut
51 asis of their detection of ammonia (NH3) and hydrogen cyanide (HCN) when the sample oven was heated t
53 and investigated the genetic architecture of hydrogen cyanide (HCN), a major component of root qualit
54 tratosphere, using satellite observations of hydrogen cyanide (HCN), a tropospheric pollutant produce
55 he production of indole-3-acetic acid (IAA), hydrogen cyanide (HCN), ammonia (NH(3)), and exopolysacc
56 ydrogen peroxide (H2O2), nitric acid (HNO3), hydrogen cyanide (HCN), hydroxymethyl hydroperoxide, per
57 ence of water (H(2)O), carbon monoxide (CO), hydrogen cyanide (HCN), methane (CH(4)), ammonia (NH(3))
58 polar or pericyclic reactions from water and hydrogen cyanide (HCN), two established prebiotic candid
64 denotes a chemical defensive strategy where hydrogen cyanide (HCN, hydrocyanic or prussic acid) is p
65 met Hyakutake with an abundance (relative to hydrogen cyanide, HCN) similar to that seen in dense int
66 e, hydrochloric acid, cyanogen chloride, and hydrogen cyanide in negative polarity are investigated.
67 ndicate a similar stability of formamide and hydrogen cyanide in solution as well as their relatively
68 -driven, six-electron catalytic reduction of hydrogen cyanide into methane and likely also ammonia.
70 e whitefly Bemisia tabaci, and the resulting hydrogen cyanide is detoxified by conversion to beta-cya
75 , carbon metabolism in Escherichia coli, and hydrogen cyanide production in the plant beneficial stra
76 Pseudomonas aeruginosa, including alginate, hydrogen cyanide production, and type IV pilus-mediated
78 ion mutation in a gene encoding a subunit of hydrogen cyanide synthase (hcnC) eliminated nematode kil
79 eruginosa PAO1 strain with a mutation in the hydrogen cyanide synthase gene cluster was much less tox
80 t tetroses and pentoses can be accessed from hydrogen cyanide through a Kiliani-Fischer-type process
85 an police QS-deficient cheaters by producing hydrogen cyanide, which is also QS regulated; however, t