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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.
6                                              Hydrogen cyanide, a gaseous molecule, is produced by whi
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
13 oday, and might have been formed solely from hydrogen cyanide and formaldehyde.
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
18                                 Avoidance of hydrogen cyanide as a by-product also improves process s
19 ment key literature results and suggest that hydrogen cyanide--"Blausaure"--was that feedstock.
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
25                                   Deuterated hydrogen cyanide (DCN) was detected in a comet, C/1995 O
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.
31                  Prunasin may be degraded to hydrogen cyanide, glucose, and benzaldehyde by the actio
32 osed of micrometre-sized particles of frozen hydrogen cyanide (HCN ice).
33      Respiration was inhibited by two gases, hydrogen cyanide (HCN) and nitric oxide (NO), whose appe
34                                      We used hydrogen cyanide (HCN) as a PA specific biomarker and aq
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(
39                                              Hydrogen cyanide (HCN) is an emerging gasotransmitter, j
40                             The chemistry of hydrogen cyanide (HCN) is believed to be central to the
41                                              Hydrogen cyanide (HCN) is coproduced with ethylene in pl
42                                              Hydrogen cyanide (HCN) is synthesized from ammonia (NH(3
43             The abundance of HNC relative to hydrogen cyanide (HCN) is very similar to that observed
44 en or chlorine (and other halogens) can form hydrogen cyanide (HCN) or hydrogen chloride (HCl) and th
45 CL activity in FRD1 contributes to increased hydrogen cyanide (HCN) production by this isolate.
46                            Quantification of hydrogen cyanide (HCN) production from laboratory isolat
47          Additionally, direct measurement of hydrogen cyanide (HCN) production showed that P. aerugin
48 lity, biofilm formation, quorum sensing, and hydrogen cyanide (HCN) production.
49                   We investigated if gaseous hydrogen cyanide (HCN) was a marker of BCC infection.
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
52 all hydrocarbons into the crystal lattice of hydrogen cyanide (HCN), a highly polar molecule.
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
59                                Here, we used hydrogen cyanide (HCN), which reacts with carbonyls to f
60  including the H2S-oxidation pathway and the hydrogen cyanide (HCN)-assimilation pathway.
61  reactive hydroxynitrile that releases toxic hydrogen cyanide (HCN).
62 ailable acetone cyanohydrin as the source of hydrogen cyanide (HCN).
63 rohydride (NaBH(3)CN) which results in toxic hydrogen cyanide (HCN).
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.
69                                              Hydrogen cyanide is a ubiquitous gas in the atmosphere a
70 e whitefly Bemisia tabaci, and the resulting hydrogen cyanide is detoxified by conversion to beta-cya
71                       Our results imply that hydrogen cyanide is the sole or primary toxic factor pro
72 e-body dissociation of sym-triazine to three hydrogen cyanide molecules.
73  one of the two-membered products acetylene, hydrogen cyanide, or N2.
74            The higher order hydrocarbons and hydrogen cyanide peak sharply in abundance and are undet
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
77                                              Hydrogen cyanide serves as a deterrent against herbivore
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
81 osition of cyanohydrins in order to generate hydrogen cyanide upon tissue damage.
82  role in chemical defense by releasing toxic hydrogen cyanide upon tissue disruption.
83                    Both molecules as well as hydrogen cyanide were found in the atmosphere of HD 2094
84 after impact, whereas those for methanol and hydrogen cyanide were unchanged.
85 an police QS-deficient cheaters by producing hydrogen cyanide, which is also QS regulated; however, t