Subject from tetrahydrofuran

Other Transient Interactions. The PVA/borax example dealt with the effects of surface exposure of a two-component polymer system to a wetting liquid. We discovered a practical example of this class of phenomena in a plasticized poly (vinyl chloride) (PVC) system. A peculiar plasticizer (tetraethyl methylene bisphosphonate) for PVC has been found (6) which has the unusual property of exuding out of PVC immediately upon exposure to high humidity. The plasticizer quickly re-enters the resin when the humidity is reduced. A film of 60% resin and 40% plasticizer was solvent cast from tetrahydrofuran onto an impedometer bar and was subjected to sudden high humidity exposure. 

Cytochalasin B (from dehydrated mould matter) [14930-96-2] M 479.6. Purified by MeOH extraction, reverse phase Cl8 silica gel batch extraction, selective elution with 1 1 v/v hexane/tetrahydrofuran, crystn, subjected to TLC and recrystallised [Lipski et al. Aruil Biochem 161 332 1987]. 

The important observation from the data in Table 3 is that NC samples subjected to acid bod followed by tetrahydrofuran (THF)-benzene treatment yielded essentially the same sulfate contents as samples subjected to THF-benzene treatment alone. From this the authors interpret that sulfate contents from THF-benzene treatments actually represent absolute values of the difficult-to-remove sulfate which may very well be true sulfate ester . It is also tentatively concluded that approximately 90% of the original sulfate content in unstabilized NC is readily removable sulfuric acid with the remainder the more difficult-to-remove sulfate ester. Dilute acid boil treatment of NC for 56 hours does not eliminate all of the free sulfuric acid and leaves the difficult-to-remove sulfate practically unchanged... 

The synthesis of tetrahydrofuran derivatives from unsaturated alcohols via hydroformylation intermediates was developed many years ago. Moderate yields are obtained from but-2-en-l,4-diol (Scheme 54)94 but hydroformylation is not the major pathway when coniferyl alcohol is subjected to the oxo process (Scheme 55).9S A more complicated reaction is involved... 

Apart from the qualitative observations made previously about suitable solvents for study, the subject of solvates has two important bearings on the topics of thermochemistry which form the main body of this review. The first is that measured solubilities relate to the appropriate hydrate in equilibrium with the saturated solution, rather than to the anhydrous halide. Obviously, therefore, any estimate of enthalpy of solution from temperature dependence of solubility will refer to the appropriate solvate. The second area of relevance is to halide-solvent bonding strengths. These may be gauged to some extent from differential thermal analysis (DTA), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC) solvates of "aprotic solvents such as pyridine, tetrahydrofuran, and acetonitrile will give clearer pictures here than solvates of "protic solvents such as water or alcohols. 

In contrast to the relative chemical stability of mono-epoxides, diol epoxides of fatty acids (10.52), which are formed from di-epoxides by EH, are subject to a different fate. In such metabolites, intramolecular nucleophilic substitution may occur, such that oxirane opening is accompanied by formation of a tetrahydrofuran ring [134], Such reactions of intramolecular nucleophilic substitution are discussed in detail in Sect. 11.9. In the case of diol epoxides of fatty acids, the resulting tetrahydrofuran-diols (10.53) are part of a much larger ensemble of oxygenated metabolites of fatty acids, the potential cytotoxicities of which are being evaluated [135]. 

System (4) has been reported for the quantitative determination of steroids in health and disease [143], Prior to analysis, free steroids were removed from the sample. Conjugated steroids were enzymatically hydrolyzed, and the liberated products extracted into 1 3 tetrahydrofuran-ethyl ether. The extract was evaporated, the residue dissolved in acetic acid, and then oxidized with sodium bismuthate. The final product was acetylated or formulated, and subjected to GC analysis along with the standard. A stabilized column of 4% LAC-2R-446 and 1% 85% phosphoric acid on... 

The behavior of electrolytes in aqueous organic mixtures, particularly those consisting of dipolar aprotic solvents (1,2, S, 4,5,6) has long been a subject of considerable importance. Interest in dipolar aprotic solvent-water mixtures arises, in part, from the recent studies of tetrahydrofuran-water mixtures (7), which involved ion-solvation and proton bonding. Because of the scarcity of... 

Finally, two tetrahydrofurofuran lignans (the stereoisomers asarinin and sesamin, Scheme 12) have been subjected to MTO-catalyzed oxidation. In both cases, the major product originates from oxidative cleavage of one of the phenyl-tetrahydrofuran bonds yielding a lactone. In a CH2Cl2/MeCN mixture using UHP as the oxidant, 65% conversion and 87% selectivity for the lactone is obtained. With immobilized MTO/PVP-2% as catalyst in CH2Cl2/EtOH, similar results are obtained [95]. 

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