ライフサイエンスコーパス: dimethylacetamide

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

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

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

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

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

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

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

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

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

13 -(6-oxo-5,6-dihydro-phenanthridin-2-yl) -N,N-dimethylacetamide (designated as PJ34) was one of the po

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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