ライフサイエンスコーパス: AcOH

1 AcOH prevents the fast coordination of ZIF-8 building bl

2 y available Langlois reagent through KMnO(4)/AcOH system.

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

4 as a hydrogen bond acceptor and acetic acid (AcOH) as a hydrogen bond donor.

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

6 EO), ZIF-8 building blocks, and acetic acid (AcOH), followed by amine-facilitated crystallization of

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

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

9 rbon nitride (MGCN), chitin and acetic acid (AcOH).

10 lid-Phase Peptide Synthesis: HCl/FeCl(3) and AcOH/FeCl(3) as Viable PFAS-Free Alternatives for TFA.

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

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

13 een sophisticated, which includes oxygen and AcOH-induced oxidative C(sp(3))-C(sp(2)) cross-dehydroge

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

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

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

17 rative products with employment of p-TSA and AcOH through a regioselective cyclization process.

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

19 cascade reaction sequence aided by catalytic AcOH.

20 product in the absence/presence of catalytic AcOH as an additive.

21 ted via the absence or presence of catalytic AcOH.

22 lucose oxidase-mimicking activity and chitin-AcOH mirrored peroxidase.

23 zymatic glucose test strips from MGCN-chitin-AcOH based hydrogel were reported and verified for semi-

24 MGCN-chitin-AcOH when in contact with glucose, oxidised glucose to g

25 ydrogen peroxide (H(2)O(2)) while the chitin-AcOH decomposed the generated H(2)O(2), as proved separa

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

27 t of Et(2)NH followed by acidic dehydration (AcOH/HCl) afforded the targeted agents 12a-j.

28 sing various co-solvents (H(2)O, MeOH, EtOH, AcOH, etc.).

29 ponse relationships on olfaction of Me-FPOSA-AcOH and PFHxS becoming more pronounced as the concentra

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

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

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

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

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

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

36 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

37 in a sealed vial in a microwave apparatus in AcOH at 200 degrees C leads to 1-hydroxy-beta-carbolines

38 At 60 degrees C in AcOH with H(2)SO(4) as catalyst, C-2 aryl indoles give 3

39 15 and reaction with 50% aqueous NH(2)OH in AcOH afforded a 9:1 mixture of cis and trans oximes, fro

40 ctured 1H-pyrazoles prepared by oxidation in AcOH.

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

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

43 In this work, we show that in 0.1 M AcOH in EtOH, aryl amines react quite efficiently at the

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

45 ds, and notably, reactions in the absence of AcOH were much slower and/or lower yielding.

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

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

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

49 The inclusion or exclusion of AcOH as an additive is the foremost cause for the positi

50 s formed in these reactions, and the role of AcOH was not desilylation but possibly only purine activ

51 yloxirane-2-carboxamides with CF(3)CO(2)H or AcOH/H(2)SO(4).

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

53 ormal dehydrative step followed by palladium AcOH-induced CH(sp(3))-CH(sp(2)) oxidative cross-couplin

54 nasal health outcomes, except serum Me-PFOSA-AcOH (OR: 1.164; 95% CI: 1.020-1.308), which significant

55 Exposure to Me-PFOSA-AcOH may be related to frequent nasal congestion, while

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

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

58 FOS and nonlinear associations with Me-PFOSA-AcOH, PFDeA, and PFNA.

59 y, we found inverse associations of Me-PFOSA-AcOH, PFOS, and the PFAS mixture only among newborns who

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

61 A copper-promoted regiodivergent, AcOH-switchable, distal and proximal direct cyanation of

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

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

64 values of extracts obtained by MAE using TBP:AcOH, 1:2 (mol/mol) were examined against those of extra

65 ional organic solvents was obtained with TBP:AcOH (1:2).

66 The computational study reveals that the AcOH that formed in the reaction medium plays a key role

67 e conditions identified (first step: toluene/AcOH = 1:1, 1 h, 50 degrees C; second step: toluene/AcOH

68 1:1, 1 h, 50 degrees C; second step: toluene/AcOH = 1:1, Fe(ClO(4))(3).H(2)O, 16 h, 50 degrees C) res

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

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

71 ertion of the in situ-generated carbene with AcOH to afford the respective acetates in high yields.

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

73 ediamines and N-alkyl nitroanilines using Zn-AcOH and HCl/MeOH, respectively.

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

75 s, which upon reductive cyclization using Zn/AcOH afforded the natural product homalicine.

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