戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 h l-cysteine, N-acetyl-l-cysteine, and allyl mercaptan.
2 an and cis-fused product from Z-homoallyllic mercaptan.
3 st formed in situ via the addition of benzyl mercaptan.
4 les, even with high levels of polyfunctional mercaptans.
5  selectively rupture into a set of monomeric mercaptans.
6 gen sulfide, 1 x 10(-4) mug/L air for methyl mercaptan, 1 x 10(-3) mug/L air for butyric acid, 1 x 10
7 thesis of these classical analogues were the mercaptans 10 and 11, which were obtained from the corre
8 rious proportions of the hydroxyl-terminated mercaptan (11-mercapto-1-undecanol).
9 , remarkable increases in the polyfunctional mercaptans, 3-mercaptohexanol (3MH) and its acetate este
10 ulfide anion or sulfur-centered radical from mercaptan 6.
11 hanism of thiol-ene reactions between methyl mercaptan and a series of 12 alkenes: propene, methyl vi
12 ding trans-fused product from E-homoallyllic mercaptan and cis-fused product from Z-homoallyllic merc
13               NG-odorant content (tert-butyl mercaptan and isopropyl mercaptan) was used to estimate
14 volatile sulfur-based odorants such as alkyl mercaptans and alkyl sulfides.
15 and methionine yields ammonia, H(2)S, methyl mercaptan, and butyrate, which are capable of arresting
16       Sulfur compounds including H2S, methyl mercaptan, and dimethyl-mono-(di;tri) sulfide are import
17 een hydrogen sulfide, thionyl carbon, methyl mercaptan, and ethyl mercaptan with silanized stainless
18 aining compounds including hydrogen sulfide, mercaptans, and sulfur dioxide.
19                VSC, and in particular methyl mercaptan, are therefore capable of inducing deleterious
20  of alkyl aryl thioethers require the use of mercaptans as the starting materials, which comes with p
21 results showed agreement of <0.6% for methyl mercaptan at 5, 10, 15, and 20 mumol/mol to the expected
22  (2-furfurylthiol), and struck flint (benzyl mercaptan), at nanogram-per-liter levels.
23            The rGOx was modified with benzyl mercaptan (BnSH) to improve the interaction with Pd clus
24 cting self-assembled monolayers of octadecyl mercaptan (C18) on the MALDI probe surface, we were able
25     Breath hydrogen sulfide (H2S) and methyl-mercaptan (CH3SH) concentrations are used as quantitativ
26 is family, hydrogen sulfide (H2S) and methyl mercaptan (CH3SH), are primarily responsible for mouth o
27 s are a class of organic sulfur derivatives (mercaptans) characterized by the presence of sulfhydryl
28 ercaptomethane-lyase, responsible for methyl mercaptan (CHSH) production by oral anaerobes.
29 e to release back hydrogen sulfide and other mercaptans during AR-aging.
30 d sensitivity were hydrogen sulfide > methyl mercaptan &gt; dimethylsulfide.
31                              However, methyl mercaptan has the greatest effect.
32 ompounds such as hydrogen sulfide and methyl mercaptan have been associated with adult periodontitis
33   It also converted benzyl bromide to benzyl mercaptan in 55% yield.
34  (Pd(0)-catalyzed thiol coupling) leading to mercaptan intermediate 18.
35           Data show that 48-hour exposure to mercaptan lowered resting intracellular pH but did not c
36 ort the hypothesis that gases such as methyl mercaptan may play a role in both surgical wound healing
37 atile compounds, volatile sulphur compounds, mercaptans, metals, anions and cations.
38 e been either a mixture of thiophenol/benzyl mercaptan, or the alkanethiol MESNA.
39      After cryogenically trapping the methyl mercaptan output stream from the permeation system into
40 ranched poly(ethylene glycol) and poly(allyl mercaptan) (PEG-PAM) polymers to generate an amphiphilic
41  aziridines with 2-bromobenzyl alcohols and -mercaptan, respectively, followed by Cu-catalyzed N-aryl
42 ment of inactivated enzyme with DTT or other mercaptans restores enzyme activity and reverses the cov
43 lfide interchange approach using sec-isoamyl mercaptan (SIT) as an alkyl sulfenyl-protecting group of
44 to dithiocarbamates (by facile addition of a mercaptan such as N-acetylcysteine) and quantitating the
45 derivatives from the coupling of homoallylic mercaptans such as hex-3-ene-1,6-dithiol with various al
46  distinguished as different classes, such as mercaptans, sulfides, thiophenes, benzothiophenes, and d
47 ve demonstrated that cells exposed to methyl mercaptan synthesize less collagen, degrade more collage
48 se the reactivity and facilitate addition of mercaptans, thereby raising inducer potencies.
49 etable VOCs, including sulfoxides, sulfides, mercaptans, thiophenes, and aldehydes.
50 atives involving conjugate addition of allyl mercaptan to an acrylate containing a tethered olefinic
51 e permeation tube was replaced with a methyl mercaptan tube (a toxic, reactive compound) in balance n
52 the presence of allyl alcohol and tert-butyl mercaptan undergo nucleophilic substitution followed by
53 he headspace above water spiked with dibutyl mercaptan was sampled with a solid phase microextraction
54  content (tert-butyl mercaptan and isopropyl mercaptan) was used to estimate that a mean NG-CH(4) con
55                  Hydrogen sulfide and methyl mercaptan were derivatized under a more stable N-ethyl m
56  crushing, extra increases in polyfunctional mercaptans were observed.
57 chieved when the terminal alkynes and benzyl mercaptans were reacted using (t)BuOLi (0.5 equiv) in Et
58                          We found that allyl mercaptan with NADPH was the preferred substrate-cofacto
59  thionyl carbon, methyl mercaptan, and ethyl mercaptan with silanized stainless steel surfaces.
60 he reaction of both cis- and trans-homoallyl mercaptans with aldehydes provided the same major diaste
61  cyclizations between homoallyl alcohols and mercaptans with aldehydes.
62 tions between a representative thiol (methyl mercaptan) with N-allyl and N-propargyl maleimide under