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1  inhibitor, 3, 4-dihydro-5-[4-(1-piperidinyl)butoxy]-1(2H)-isoquinolinone (DPQ; IC50=1 microM/l) was
2 RP inhibitor 3,4-dihydro-5-[4-(1-piperidinyl)butoxy]-1(2H)-isoquinolinone both showed increased resis
3 er by 10 muM 3,4-dihydro-5-[4-(1-piperidinyl)butoxy]-1(2H)-isoquinolinone, an established PARP inhibi
4 RP inhibitor 3,4-dihydro-5-[4-(1-piperidinyl)butoxy]-1(2h)-isoquinolinone.
5 ic inhibitor 3,4-dihydro-5-[4-(1-piperidinyl)butoxy]-1(2h)-isoquinolinone.
6 ist (R)-3-{4-[3-(4-chloro-2-phenoxy-phenoxy)-butoxy]-2-ethyl-phenyl}-propionic acid (20) for the trea
7 ble L-glutamic acid derivative, (4S)-5-(tert-butoxy)-4-[(tert-butoxycarbonyl)amino]-5- oxopentanoic a
8                                         tert-Butoxy-(4-phenyl-quinolin-3-yl)-acetic acids (tBPQA) are
9            The 5'-methoxy, 5'-ethoxy, and 5'-butoxy analogs of 2,5,6-trichloro-1-(beta-D-ribofuranosy
10  blocked by the pan-caspase inhibitor N-tert-butoxy-carbonyl-Val-Ala-Asp-fluoro methylketone (zVAD-fm
11          Three chiral alpha-(nonafluoro-tert-butoxy)carboxylic acids (R)-1, (RS)-2, (R)-3 were synthe
12         Paramagnetic (13)C NMR shifts of the butoxy chains as well as all (1)H NMR chemical shifts ar
13 ong the compounds studied, n-butyl- and/or n-butoxy-containing guanidines showed superior biological
14 t-membered ring in the anion radical of tert-butoxy-COT.
15                              Compound 3, the butoxy derivative, had a lower target-to-nontarget ratio
16 performed at 120-130 degrees C, whereas tert-butoxy derivatives undergo the retro-ene reaction at 90
17                                              Butoxy increases in surface concentration over Pt(111) w
18 y at the 2'-ribose position linked through a butoxy linker.
19 fied a substituted quinazolinone (Quin-C1, 4-butoxy-N-[2-(4-methoxy-phenyl)-4-oxo-1,4-dihydro-2H-quin
20 opoxy group of 2c was preferred over ethoxy, butoxy, or pentoxy.
21 y-3-propyl-4-[4-[4-(2H-tetrazol-5-yl)phenoxy]butoxy]phenyl) ethanone (4).
22   These mechanistic data imply that the tert-butoxy radical reacts with the C-H bonds of alkanes, and
23 oportionation pathway, catalyzed by the tert-butoxy radical, of mixed peroxides for the formation of
24 cal traps support the intermediacy of a tert-butoxy radical, which forms an alkyl radical intermediat
25 is the C-H cleavage of cyclohexane by a tert-butoxy radical.
26 mply that C-H bond cleavage occurs by a tert-butoxy radical.
27 to vapors of trimethylaluminum and tris(tert-butoxy)silanol deposits highly conformal layers of amorp
28  supported by sterically demanding tris(tert-butoxy)siloxide ligands induces a large cooperative effe
29 uced via grafting reactions of the tris(tert-butoxy)siloxy iron(III) complex Fe[OSi(O(t)Bu)(3)](3)(TH
30                                The tris(tert-butoxy)siloxy titanium complexes Ti[OSi(O(t)Bu)(3)](4) (
31 ction between the methyl hydrogens on a tert-butoxy substituent and the cyclooctatetraene (COT) ring
32 mics of nickel(II) phthalocyanine with eight butoxy substituents, NiPc(OBu)8.
33  of sulfonyl halide derivatives of (S)-(tert-butoxy)-[(tert-butoxycarbonyl)amino]oxoalkanoic acids.
34 ,5-bis{4-[di(p-anisyl)amino]styryl}-3,4-di(n-butoxy)thiophene, [1](2+) and [2](2+) respectively.
35 ndium tin oxide (ITO) reacts with tetra(tert-butoxy)tin to give surface bound alkoxytin species.
36  [(R)-3,3'-dibromo-2,2'-binaphthoxy](di-tert-butoxy)titanium(IV) (R-3) exists as a crystallographic C
37 ) or pentane (17-19); OR(f) = perfluoro-tert-butoxy) via photolysis of the precursor complex [(HEB)Re

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