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1 arios of, respectively, copper, cadmium, and tributyltin.
2 stropod molluscs which led to the banning of tributyltin.
3 ent perilymphatic solutions or by the use of tributyltin, a chloride ionophore, we found alterations
4 d by an electroneutral mechanism mediated by tributyltin, a potent inhibitor of IMAC.
5 of the methyl farnesoate receptor, MfR), and tributyltin (agonist of the retinoid X acid receptor, RX
6 e prepared by radioiododestannylation of the tributyltin analogues in high yields, radiochemical puri
7 ept-2-ene (4) followed by elimination of the tributyltin and p-tolylsulfonyl groups using tetrabutyla
8                                   It detects tributyltin and triphenyltin in nanomolar concentrations
9 enerated from the corresponding bromide with tributyltin and tris(trimethylsilyl)silyl radicals and s
10 hemicals including, perfluoro-octanoic acid, tributyltin, and butylhydroxytoluene, in endocrine-activ
11      "Catalytic" tin hydride, generated from tributyltin chloride and excess polymethylhydrosiloxane
12 ived from hiPSCs, but endosulfan sulfate and tributyltin chloride did not.
13 f methyl iodide, trimethylsilyl chloride, or tributyltin chloride gives mixtures of alpha-substituted
14 tized for further study (endosulfan sulfate, tributyltin chloride, fenpropimorph, and spiroxamine).
15 r electrophiles (acylsilanes, chlorosilanes, tributyltin chloride, iodine) cleanly provides practical
16 onmental contaminants methoxychlor, lindane, tributyltin chloride, pentachlorophenol, diuron, and eth
17 n of trans-2-fluoro-1-bromocyclopentane with tributyltin deuteride.
18       Furthermore it was possible to measure tributyltin directly in untreated spiked sediments.
19  copper pyrithione (CuPT), an alternative to tributyltin for antifouling paint biocides, inhibits the
20 ted by the reaction of an organic azide with tributyltin hydride (Bu(3)SnH) in the presence of substo
21 a-(phosphatoxy)alkyl radicals on exposure to tributyltin hydride and AIBN in benzene at reflux.
22 ion reactions, and subsequent treatment with tributyltin hydride and azoisobutyronitrile brought abou
23 zyl pyrrolidines examined in the presence of tributyltin hydride and azoisobutyronitrile in benzene a
24 logues (S)-5 and (R)-5 was accomplished with tributyltin hydride in mixed aqueous solvents in the pre
25  chlorides were synthesized and reacted with tributyltin hydride in the presence of AIBN to generate
26      Following glycosylation, treatment with tributyltin hydride in toluene at reflux brings about re
27 on of resin-bound primary alkyl radical with tributyltin hydride is about 2 times slower than that of
28                                              Tributyltin hydride mediated addition of 3-iodosalicylal
29                                              Tributyltin hydride reduction of bromohydrins 7a,b and 1
30 pt-2-ene (5), which involved the addition of tributyltin hydride to 7-tert-butoxycarbonyl-2-p-toluene
31 iastereoisomer that may either be trapped by tributyltin hydride to afford the 2,4,5-trisubstituted p
32 s in the presence of the hydrogen atom donor tributyltin hydride, 2',3'-dideoxythymidine is formed in
33  dichlorides 10-12 and, after reduction with tributyltin hydride, the diindeno-fused 4H-cyclopenta[de
34 ine component in Ugi-4CR followed by an AIBN/tributyltin hydride-induced radical reaction.
35 ion: see text] The benzeneselenol-catalyzed, tributyltin hydride-mediated addition of phenolic iodide
36                       [structures: see text] Tributyltin hydride-mediated cyclizations of 1-nitro-2-a
37                                              Tributyltin hydride-mediated radical cyclization of 4-6
38 or hazardous reagents and initiators such as tributyltin hydride.
39 hiometric amounts of toxic reagents, such as tributyltin hydride.
40 nmentally friendly alternative to the use of tributyltin hydride.
41 lly requires stoichiometric reagents such as tributyltin hydride.
42 rin with a one-carbon synthon (hydroxymethyl tributyltin or CO) to give a 13-, 15-, or 3,13-formylchl
43  Of the 223 chemicals monitored, pesticides, tributyltin, polycyclic aromatic hydrocarbons, and bromi
44 radicals were generated by the addition of a tributyltin radical to alkyne moieties, followed by radi
45 vities of R- and P-communities to prometryn, tributyltin (TBT) and N-phenyl-2-naphthylamine (PNA) wer
46  their environment, then they may accumulate tributyltin (TBT) during their juvenile period, which ne
47                                              Tributyltin (TBT) is a persistent and bioaccumulative en
48    We have previously shown that exposure to tributyltin (TBT) modulates critical steps of adipogenes
49   This study examined effects of hypoxia and tributyltin (TBT) on adult Eastern oysters (Crassostrea
50 how that exposure of F0 mice to the obesogen tributyltin (TBT) throughout pregnancy and lactation pre
51 at-great-grandsons of female mice exposed to tributyltin (TBT) throughout pregnancy and lactation wer
52  conductance and use the environmental toxin tributyltin (TBT) to better understand Cl-prestin intera
53                      The biomagnification of tributyltin (TBT), dibutyltin (DBT), monobutyltin (MBT),
54                              Mono-, di-, and tributyltin were measured in three sediment CRMs at conc
55 ntration addition model, and combinations of tributyltin with juvenoids resulted in greater than addi