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Decalins nitration

Decalin and derivs 3 D21—D22 decalin hydroperoxide 3 D22 decalin nitrated derivs 3 D22... [Pg.536]

Chemical Properties and Reactivity. LLDPE is a saturated branched hydrocarbon. The most reactive parts of LLDPE molecules are the tertiary CH bonds in branches and the double bonds at chain ends. Although LLDPE is nonreactive with both inorganic and organic acids, it can form sulfo-compounds in concentrated solutions of H2SO4 (>70%) at elevated temperatures and can also be nitrated with concentrated HNO. LLDPE is also stable in alkaline and salt solutions. At room temperature, LLDPE resins are not soluble in any known solvent (except for those fractions with the highest branching contents) at temperatures above 80—100°C, however, the resins can be dissolved in various aromatic, aUphatic, and halogenated hydrocarbons such as xylenes, tetralin, decalin, and chlorobenzenes. [Pg.395]

Corey s retrosynthetic concept (Scheme 9) is based on two key transformations a cationic cyclization and an intramolecular Diels-Alder (IMDA) reaction. Thus, cationic cychzation of diene 50 would give a precursor 49 for epf-pseudo-pteroxazole (48), which could be converted into 49 via nitration and oxazole formation. Compound 50 would be obtained by deamination of compound 51 and subsequent Wittig chain elongation. A stereocontroUed IMDA reaction of quinone imide 52 would dehver the decaline core of 51. IMDA precursor 52 should be accessible by amide couphng of diene acid 54 and aminophenol 53 followed by oxidative generation of the quinone imide 52 [28]. [Pg.21]

The nitration of chiral alkanes producing racemic nitro compounds, and that of cis-and frans-decalin, both leading to the formation of trans-9-nitrodecalin,170 support the involvement of alkyl radicals. [Pg.591]

Ref Beil 5, [60] 251 9,10-Dinitro-trans-decalin, C10H)gN204 mw 228.24, N 12.27% crysts (from ale), mp 167° (dec) obtd with other products by nitration of decalin (Refs 1 2). Its expl props were not detd... [Pg.444]

Supported liquid membranes, consisting of an organic solution of -octyl(phenyl)-A,iV-diisobutylcarbamoylmethylpho-sphine oxide (CMPO) and tributyl-phosphate (TBP) in decalin, were capable of selective separation and concentration of actinide and lanthanide ions from aqueous nitrate feed solutions and from synthetic nuclear wastes where the strip solution is a mixture of formic acid (FA) and hydroxylammonium formate (HAF) [106,107]. TBP is added to CMPO to improve its solubility in aliphatic diluents. Although low concentration of nitric acid was initially used as the strippant solution, a gradual... [Pg.899]

Liquid and solid samples are placed in an opened cup while volatile samples are placed in a gelatine capsule and placed in the cup as for a normal sample. A suitable absorption solution is placed at the bottom of the bomb along with the prepared sample. It may be necessary to include an aid with combustion resistant samples as a support to combustion and such additives are low molecular weight paraffin oils, ammonium nitrates, benzoic acid, decalin, etc. [Pg.73]

Complexes containing the fragment Cp Ir (Cp is pentamethylcyclopentadienyl) are active precatalysts in the C-H oxidation of cw-decalin and cyclooctane. Ceric ammonium nitrate was a sacrificial oxidant and water was the oxygen source... [Pg.3]


See other pages where Decalins nitration is mentioned: [Pg.360]    [Pg.47]    [Pg.444]    [Pg.443]    [Pg.1012]    [Pg.122]    [Pg.87]    [Pg.444]    [Pg.383]    [Pg.87]    [Pg.27]    [Pg.30]    [Pg.158]    [Pg.2907]   
See also in sourсe #XX -- [ Pg.592 ]




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Decalin

Decalins

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