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N-methylformamide

The idea is to have everything in place before the oxygen is applied. So, lOOg of safrole is in the addition funnel and stirring around in the reaction flask are 10.6g of PdCU, 60g CuCI and 500mL of aqueous dimethylformamide (made by mixing 62.5mL dH20 and 437,5mL DMF). Dimethylformamide (DMF) is not the same as the watched chemical known as N-methylformamide. [Pg.62]

Dehydration of N-methylformamide by />-toluenesulfonyl chloride quinoline to form methyl isocyanide, 46,75... [Pg.126]

DMSO, dimelhyltulfoxide. DMF, dimethyl fomumiiie. PC, propylene carbonate. AN. acetonitrile. AC. acetone NMF, N methylformamide... [Pg.34]

Beere, H.M., Morimoto, R.I., Hickman, J.A. (1993). Investigations of mechanisms of drug-induced changes in gene expression N methylformamide-induced changes in synthesis of the M(r) 72,000 constitutive heat shock protein during commitment of HL-60 cells to granulocyte differentiation. Cancer Res. 53, 3034—3039. [Pg.451]

N-Methylformamide in urine Ethyl benzene End of shift 40 mg/g creatinine ... [Pg.98]

The ready exchange of silyl groups is apparent from the reaction of equimolecu-lar amounts of trimethylsilyl formate 148 with N-triethylsilyhnethylamine 163 for 1 h at room temperature (Scheme 4.4) whereupon two layers separate the upper layer consists of HMDSO 7 and l,l,l-trimethyl-3,3,3-triethyldisiloxane 64 and the lower layer contains N-methylformamide 164 in almost quantitative yield [5]. [Pg.43]

Villemin has reported the use of sodium tetraphenylborate as a stable reactant for Suzuki couplings performed in water or N-methylformamide (NMF) as solvents (Eq. 11.25) [40],... [Pg.391]

These include hydrazine, dimethylsulfoxide (DMSO), formamide and some derivatives (N-methylformamide and dimethylformamide), acetamide and some derivatives, and pyridine N-oxide. Some salts such as potassium acetate also intercalate kaolinites. Once intercalated by one of these small molecules or salts, other molecules which normally do not directly intercalate kaolins can be introduced by replacement. Further, the exposure of the inner surfaces by intercalation gives one the opportunity to alter the interlayer bonding of the kaolin layers by chemical modification of the inner surfaces. [Pg.44]

Figure 3. Variations of the tautomerism equilibrium constant Kr ([B] = 0.3 mole l 1, 30°C) of t-butyl-2-picolyl (0) and quinaldyl (A) ketones vs. solvent polarity. (DME) dimethoxyethane (CFG) propyleneglycol carbonate (NMF) N-methylformamide (F)formamide. Figure 3. Variations of the tautomerism equilibrium constant Kr ([B] = 0.3 mole l 1, 30°C) of t-butyl-2-picolyl (0) and quinaldyl (A) ketones vs. solvent polarity. (DME) dimethoxyethane (CFG) propyleneglycol carbonate (NMF) N-methylformamide (F)formamide.
As has been discussed, ordinary formamides have a barrier of about 21 kcal/ mol, which is a little less than that required for the isolation of atropisomers at room temperature. This means that, at a temperature slightly lower than ambient, it may be possible to obtain stable rotamers. This possibility was first realized by Gutowsky, Jonas, and Siddall (40). They used a uranyl nitrate complex of N-benzyl-N-methylformamide (4) crystallized from dichloromethane. When the crystals were washed with ice water to strip off the uranyl nitrate, a mixture of E and Z forms (Z/E = 1.6) was obtained. Since the equilibrium mixture gives a Z/E value of 0.8, it was possible to perform a kinetic study of equilibration... [Pg.13]

CHLOROETHANOL ETHYL FLUORIDE ETHYL IODIDE ETHYLENEIMINE ACETAMIDE N-METHYLFORMAMIDE NITROETHANE ETHYL-NITRATE ETHANE... [Pg.59]

The recent introduction of non-aqueous media extends the applicability of CE. Different selectivity, enhanced efficiency, reduced analysis time, lower Joule heating, and better solubility or stability of some compounds in organic solvent than in water are the main reasons for the success of non-aqueous capillary electrophoresis (NACE). Several solvent properties must be considered in selecting the appropriate separation medium (see Chapter 2) dielectric constant, viscosity, dissociation constant, polarity, autoprotolysis constant, electrical conductivity, volatility, and solvation ability. Commonly used solvents in NACE separations include acetonitrile (ACN) short-chain alcohols such as methanol (MeOH), ethanol (EtOH), isopropanol (i-PrOH) amides [formamide (FA), N-methylformamide (NMF), N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMA)] and dimethylsulfoxide (DMSO). Since NACE—UV may present a lack of sensitivity due to the strong UV absorbance of some solvents at low wavelengths (e.g., formamides), the on-line coupling of NACE... [Pg.488]

Valko, I. E., Siren, H., and Riekkola, M. L. (1997). Determination of association constants of dansyl-amino acids and beta-cyclodextrin in N-methylformamide by capillary electrophoresis. Electrophoresis 18, 919-923. [Pg.511]

Geiser, L., Cherkaoui, S., and Veuthey, J. L. (2002). Potential of formamide and N-methylformamide in nonaqueous capillary electrophoresis coupled to electrospray ionization mass spectrometry. Application to the analysis of P-blockers. /. Chromatogr. A 979, 389—398. [Pg.511]


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