ライフサイエンスコーパス: AcOH

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1 hamster brain homogenates to 1% SDS and 0.5% AcOH at room temperature resulted in a reduction of prio

2 any [Ni(II)(X)(L)](-) and NaOCl/acetic acid (AcOH) or cerium ammonium nitrate ((NH4)2[Ce(IV)(NO3)6],

3 ranched polyamine dendrimers in acetic acid (AcOH), we investigated the inactivation of prions by sod

4 inal oxidant in the presence of acetic acid (AcOH).

5 presence of the Pd(OAc)2 catalyst, AgOAc and AcOH directly afforded the corresponding multiple beta-C

6 hiometric oxidant, and a mixture of DMSO and AcOH as the solvent.

7 in the presence of acids such as PyH(+) and AcOH.

8 late with release of 1 equiv of pyridine and AcOH from the catalyst center, (2) alkene insertion into

9 When various concentrations of SDS and AcOH were tested, the duration and temperature of exposu

10 hibits a first-order dependence on [Co] and [AcOH], but no dependence on [O2] or [Fc*].

11 orination reactions observed in the 1/ClO(-)/AcOH catalytic system.

12 known to have little reactivity under STAB-H/AcOH conditions.

13 or substrate oxidation in the (L)Fe(II)/H2O2/AcOH catalytic system.

14 idyl-2-methyl)amine) ligand family with H2O2/AcOH or AcOOH at -40 degrees C reveal the formation of a

15 dimethylaminoborane, and acidolysis with HBr/AcOH yielded 2-L-[5-[N-(2-acetamido-4(3H)-oxopyrido[2, 3

16 labile carbamate 2d was deprotected with HCl/AcOH to provide 1, while trifluoroacetic acid was requir

17 initro-1,2-benzisothiazoles (50% H(2)O(2) in AcOH) afforded the corresponding S-oxides and S, S-dioxi

18 Oxidation of 3b or 14c,d with Pb(OAc)(4) in AcOH for 20 min at 25 degrees C and 1 h at 75 degrees C

19 15 and reaction with 50% aqueous NH(2)OH in AcOH afforded a 9:1 mixture of cis and trans oximes, fro

20 f lead in soils is measured using 0.43 mol/L AcOH as extractant.

21 igonucleotide was effected in buffered 0.1 M AcOH (pH 3.8) within 30 min at 90 degrees C.

22 tion of nitronyl nitroxide 3 in system NaNO2-AcOH yielded corresponding iminonitroxide 4.

23 Only a substoichiometric amount of AcOH is required as an additive that is both low-cost an

24 n, (4) irreversible reductive elimination of AcOH, and (5) aerobic oxidation of palladium(0) to regen

25 elease of NO and H2O triggered by 1 equiv of AcOH implicates that nitrite-to-nitric oxide conversion

26 with hydrogen peroxide in MeOH, THF, MeCN or AcOH to form the corresponding C-N coupled products, N-R

27 rfluorooctane sulfonamido) acetate (Me-PFOSA-AcOH) were 26-36% lower in children of black mothers com

28 rfluorooctane sulfonamido) acetate (Me-PFOSA-AcOH), perfluorodecanoate (PFDeA), perfluorononanoate (P

29 approximately 40 mM, rt, CH2Cl2, piperidine/AcOH/molecular sieves) of a dihydrodipyrrin-carboxaldehy

30 nder reductive conditions (3-nitropyrrole/Sn/AcOH/trifluoromethyl-beta-diketone) the alpha-1H-pyrrolo

31 troalkenes in the presence of SbCl(3), TBAF, AcOH, and a catalytic amount of Pd(OAc)(2), in CH(3)CN a

32 A mild and unique AcOH(cat.)/AcCl system was found to promote an autocatal

33 mation, the best results were obtained using AcOH to afford the corresponding Mannich products in hig

34 of donor-acceptor cyclopropanes with the Zn-AcOH reductive system was developed.

35 A Zn/AcOH-mediated reduction of the nitro functionality follo

36 rated upon ozonolysis can be reduced with Zn/AcOH to afford the carbonyl compounds.

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