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1 arios of, respectively, copper, cadmium, and tributyltin.
2 ent perilymphatic solutions or by the use of tributyltin, a chloride ionophore, we found alterations
3 d by an electroneutral mechanism mediated by tributyltin, a potent inhibitor of IMAC.
4 of the methyl farnesoate receptor, MfR), and tributyltin (agonist of the retinoid X acid receptor, RX
5 e prepared by radioiododestannylation of the tributyltin analogues in high yields, radiochemical puri
6 ept-2-ene (4) followed by elimination of the tributyltin and p-tolylsulfonyl groups using tetrabutyla
7                                   It detects tributyltin and triphenyltin in nanomolar concentrations
8 enerated from the corresponding bromide with tributyltin and tris(trimethylsilyl)silyl radicals and s
9 hemicals including, perfluoro-octanoic acid, tributyltin, and butylhydroxytoluene, in endocrine-activ
10      "Catalytic" tin hydride, generated from tributyltin chloride and excess polymethylhydrosiloxane
11 f methyl iodide, trimethylsilyl chloride, or tributyltin chloride gives mixtures of alpha-substituted
12 r electrophiles (acylsilanes, chlorosilanes, tributyltin chloride, iodine) cleanly provides practical
13 n of trans-2-fluoro-1-bromocyclopentane with tributyltin deuteride.
14       Furthermore it was possible to measure tributyltin directly in untreated spiked sediments.
15  copper pyrithione (CuPT), an alternative to tributyltin for antifouling paint biocides, inhibits the
16 a-(phosphatoxy)alkyl radicals on exposure to tributyltin hydride and AIBN in benzene at reflux.
17 ion reactions, and subsequent treatment with tributyltin hydride and azoisobutyronitrile brought abou
18 zyl pyrrolidines examined in the presence of tributyltin hydride and azoisobutyronitrile in benzene a
19 logues (S)-5 and (R)-5 was accomplished with tributyltin hydride in mixed aqueous solvents in the pre
20  chlorides were synthesized and reacted with tributyltin hydride in the presence of AIBN to generate
21      Following glycosylation, treatment with tributyltin hydride in toluene at reflux brings about re
22 on of resin-bound primary alkyl radical with tributyltin hydride is about 2 times slower than that of
23                                              Tributyltin hydride mediated addition of 3-iodosalicylal
24                                              Tributyltin hydride reduction of bromohydrins 7a,b and 1
25 pt-2-ene (5), which involved the addition of tributyltin hydride to 7-tert-butoxycarbonyl-2-p-toluene
26 iastereoisomer that may either be trapped by tributyltin hydride to afford the 2,4,5-trisubstituted p
27 s in the presence of the hydrogen atom donor tributyltin hydride, 2',3'-dideoxythymidine is formed in
28  dichlorides 10-12 and, after reduction with tributyltin hydride, the diindeno-fused 4H-cyclopenta[de
29 ion: see text] The benzeneselenol-catalyzed, tributyltin hydride-mediated addition of phenolic iodide
30                       [structures: see text] Tributyltin hydride-mediated cyclizations of 1-nitro-2-a
31                                              Tributyltin hydride-mediated radical cyclization of 4-6
32 hiometric amounts of toxic reagents, such as tributyltin hydride.
33 nmentally friendly alternative to the use of tributyltin hydride.
34 rin with a one-carbon synthon (hydroxymethyl tributyltin or CO) to give a 13-, 15-, or 3,13-formylchl
35  Of the 223 chemicals monitored, pesticides, tributyltin, polycyclic aromatic hydrocarbons, and bromi
36 vities of R- and P-communities to prometryn, tributyltin (TBT) and N-phenyl-2-naphthylamine (PNA) wer
37  their environment, then they may accumulate tributyltin (TBT) during their juvenile period, which ne
38    We have previously shown that exposure to tributyltin (TBT) modulates critical steps of adipogenes
39 how that exposure of F0 mice to the obesogen tributyltin (TBT) throughout pregnancy and lactation pre
40  conductance and use the environmental toxin tributyltin (TBT) to better understand Cl-prestin intera
41                      The biomagnification of tributyltin (TBT), dibutyltin (DBT), monobutyltin (MBT),
42                              Mono-, di-, and tributyltin were measured in three sediment CRMs at conc
43 ntration addition model, and combinations of tributyltin with juvenoids resulted in greater than addi

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