ライフサイエンスコーパス: dimethylacetamide

1 ith greater amide resonance than that of N,N-dimethylacetamide.

2 tial amidicity equivalent to 73% that of N,N-dimethylacetamide.

3 interchange similar to that reported for N,N-dimethylacetamide.

4 ne counterpart, via C-N bond cleavage of N,N-dimethylacetamide.

5 of oxidized hemiaminal impurities within N,N-dimethylacetamide.

6 te lifetime (135 ps in DMF and 180 ps in N,N-dimethylacetamide) among the nine examples reported here

7 organic solvents (N,N-dimethylformamide, N,N-dimethylacetamide and N-methyl-2-pyrrolidone), and witho

8 he difference in amide resonance between N,N-dimethylacetamide and the target amide using an isodesmi

9 in D(2)O for deprotonation of acetamide, N,N-dimethylacetamide, and acetate anion by deuterioxide ion

10 to have amidicities at least as high as N,N-dimethylacetamide, and the beta-lactam system is planar

11 << methyl ethyl sulfone < acetonitrile < N,N-dimethylacetamide approximately N-methylacetamide approx

12 absorption spectra of 2-4 in CH(2)Cl(2) and dimethylacetamide are similar to those of N-confused tet

13 foxide before methyl iodide, or by using N,N-dimethylacetamide as the solvent.

14 ency of the reaction, with K(3)PO(4) and N,N-dimethylacetamide being the optimal base and solvent, re

15 etrakis(4-(pyridin-4-yl)phenyl)ethene, DMA = dimethylacetamide) crystallizes in a new structure type

16 -(6-oxo-5,6-dihydro-phenanthridin-2-yl) -N,N-dimethylacetamide (designated as PJ34) was one of the po

17 aliphatic amines in pure dimethylformamide, dimethylacetamide, dimethyl sulfoxide, or propylene carb

18 of the various modifiers (DMF, thiodiglycol, dimethylacetamide, dimethylsulfoxide, and N-methylpyrrol

19 Previously, we reported that N, N-dimethylacetamide (DMA) and N, N-dimethylformamide (DMF)

20 g mixed aqueous-aprotic dipolar solvent (N,N-dimethylacetamide (DMA) and N,N-dimethylformamide (DMF),

21 ons from N,N-dimethylformamide (DMF) and N,N-dimethylacetamide (DMA) by the cumyloxyl (CumO(*)) and b

22 Here, we report that N,N-dimethylacetamide (DMA) containing lithium chloride (LiC

23 a novel use of a common organic solvent, N,N-dimethylacetamide (DMA) in preventing inflammation-media

24 queous-organic solvent system containing N,N-dimethylacetamide (DMA) or N,N-dimethylformamide (DMF) w

25 *)) with N,N-dimethylformamide (DMF) and N,N-dimethylacetamide (DMA) was studied by laser flash photo

26 methyl N,N-dimethylcarbamate (MDMC) and N, N-dimethylacetamide (DMA) were carried out using a continu

27 Li anode in the presence of the solvent, N,N-dimethylacetamide (DMA), by employing a salt, lithium ni

28 -H bonds of N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMA), N-formylpyrrolidine (FPRD), and

29 e found that the common organic solvent, N,N-dimethylacetamide (DMA), prevents endotoxin-induced pret

30 The common excipient, N,N-dimethylacetamide (DMA), prevents imminent endotoxin-ind

31 Cryoprotectants, 8% methanol and 10% dimethylacetamide (DMA), reduced the motility over the c

32 ic products under ruthenium catalysis in N,N-dimethylacetamide (DMA).

33 The use of dimethylacetamide (DMAc) is essential for the successful

34 rmal reactions in dimethylformamide (dmf) or dimethylacetamide (dmac) with acetic acid or formic acid

35 nds in both dichloromethane (CH(2)Cl(2)) and dimethylacetamide (DMAc).

36 The ZIF-8 membrane features dimethylacetamide entrapped ZIF-8 crystals retaining the

37 tabilization and amidicities relative to N,N-dimethylacetamide for a wide range of acyclic and cyclic

38 A 72-hour infusion of 9-AC dimethylacetamide formulation was administered every 21

39 enzaldehyde and benzyl phenyl sulfone in N,N-dimethylacetamide gave 1,2-diphenyl-1-phenylsulfonylethy

40 um tetrafluoroborate and silver carbonate in dimethylacetamide has been described.

41 ha-C(sp(3))-H containing amides, such as N,N-dimethylacetamide, N,N-dimethylbenzamide, N-methylacetam

42 Coadsorption of smaller amounts of dimethylacetamide (PA = 217 kcal/mol) also produced no r

43 the cation position have been tested in N,N'-dimethylacetamide solvent (DMA) using 1,3-dimethyl-2-phe

44 hyl O-(p-nitrophenyl)thiocarbamate 1a in N,N-dimethylacetamide solvent.

45 n of GFP with 2-diazo-2-(p-methylphenyl)-N,N-dimethylacetamide was efficient.

46 a-2-adamantanone with zero amidicity and N,N-dimethylacetamide with 100% amidicity.