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Hydroperoxides halides

Alkyl halides, hydroperoxide synthesis, 327-8 Alkyl hydroperoxides anion ligands, 114-19 covalent radii, 114, 118-19 dihedral angles, 119 geometric parameters, 115-8 tetrahedral distortion, 119 artemisinin formation, 133-4 chlorotriorganosilane reactions, 779-83 crystal structure, 105-14 anomeric effect, 110-11 geometric parameters, 106-9 hydrogen bonding, 103-5, 111-14 tetrahedral distortion, 110 determination, 674... [Pg.1441]

Diacyl peroxides and acyl hydroperoxides can similarly be prepared from acyl halides or anhydrides... [Pg.492]

Another useful oxidative reaction in aqueous medium is the cleavage of cyclic ketones by hydrogen peroxide in the presence of Fe(II) salts (Eq. 8.25). The reaction proceeds through an a-hydroxy hydroperoxide, leading to a variety of products.50 The presence of Fe(II) salts decomposes the intermediate, generating a radical. In the presence of halide ions, the radical leads to synthetically useful halocarboxylic acids.51... [Pg.224]

The effect of steric crowding on the rates of reaction of the Ni1 tetraaza macrocycle complex [Ni(dmc)]+ with organic halides and hydroperoxides has also been examined. Reaction with this complex was found to be about 104 times slower than with the corresponding [Ni(tmc)]+ complex.2329... [Pg.483]

Dialkyl peroxides can be obtained by the alkylation of alkyl hydroperoxides with alkyl halides. Mild conditions can be achieved by assisting the departure of the halide ion with the aid of a suitable silver salt (Eq. 19)3S). [Pg.137]

Cyclic enone, 12 185 Cyclic ethers, 10 567, 569 12 663 polymerization, 14 271 Cyclic fatigue, in ceramics, 5 633-634 Cyclic gas generators, 6 786-787, 789, 827 Cyclic halides, 19 56 Cyclic hexakis(thio-l,4-phenylene), melt polymerization of, 23 705 Cyclic hydrocarbons, 13 687 Cyclic hydroxyalkyl alkyl peroxide, 18 454 Cyclic ion exchange operation, 14 408-413 Cyclic ketones, 12 176, 177 14 590-592. See also Cyclic 1,2-diketones physical properties of, 14 591t hydroxyalkyl hydroperoxides from, 18 450... [Pg.241]

The tin hydrides react with oxygen to give tin hydroxides, presumably via the tin hydroperoxides, and this reaction has been used for converting alkyl halides into 170- and lsO-Iabeled alcohols (Equation (146)).434 435... [Pg.855]

More recently, a novel type of halogenating enzyme, named hydroperoxide halolyase, which generates halogenated aldehydes, has been described in the marine diatom Stephanopyxis turris (Wichard and Pohnert 2006). In other microalgae, halogenation of organic compounds was shown to mainly involve methyl halide transferases (Moore et al. 1996 Manley 2002), and no vHPO has yet been identified on genomic data obtained from diatoms (Scala et al. 2002 Armbrust et al. 2004). Clearly, these emissions are not directly associated with an oxidative burst. [Pg.255]

Frimer, A. A., J. Org. Chem., 1977, 42, 3194-3196, footnote 7 A new method of preparation involves interaction of ally lie halides in solvents with 98% hydrogen peroxide in presence of silver ion and base at ambient temperature under argon. The reactions must be run in the dark to prevent precipitation of metallic silver, which will catalyse decomposition of the hydroperoxide or excess hydrogen peroxide. In an experiment not run in the dark, the hydroperoxide from 3-chlorocyclohexene ignited spontaneously after isolation and concentration. [Pg.53]

Anderson, L. R. et al., J. Fluorine Chem., 1976, 7, 481-500 Five derivatives, including the 0-0 lithium or sodium salts of the hydrogen peroxide adduct of hexafluoroacetone (2-hydroxyhexafluoro-2-propyl hydroperoxide), and their reaction products with acyl halides, are less flammable or explosive than their hydrocarbon analogues, though less stable than the parent hydroperoxides. Relevant entries are ... [Pg.158]

Results of a chemical activation induced by ultrasound have been reported by Nakamura et al. in the initiation of radical chain reactions with tin radicals [59]. When an aerated solution of R3SnH and an olefin is sonicated at low temperatures (0 to 10 °C), hydroxystannation of the double bond occurs and not the conventional hydrostannation achieved under silent conditions (Scheme 3.10). This point evidences the differences between radical sonochemistry and the classical free radical chemistry. The result was interpreted on the basis of the generation of tin and peroxy radicals in the region of hot cavities, which then undergo synthetic reactions in the bulk liquid phase. These findings also enable the sonochemical synthesis of alkyl hydroperoxides by aerobic reductive oxygenation of alkyl halides [60], and the aerobic catalytic conversion of alkyl halides into alcohols by trialkyltin halides [61]. [Pg.91]

Literature procedures for the synthesis of hydroperoxides include the preparation from hydrogen peroxide (via reaction with alkyl halides, -phosphites, -suEonates, alkenes. [Pg.309]

SCHEME 7. Synthesis of hydroperoxides from electrochemically generated superoxide and alkyl halides... [Pg.315]

Unsymmetrical dialkyl peroxides can be prepared by several methods. Some of them are summarized in Scheme 31. Primary " , secondary or tertiary"" " alkyl hydroperoxides can serve as substrates and are converted to the dialkyl peroxides by acid- or base-catalyzed nucleophilic substitution with alkylating agents like dialkyl sulfate " , diazomethane " , dialkyl sulfites, alcohols " or alkyl halides (e.g. in the presence of silver trifluoroacetate) "". An overview of the results obtained utilizing the method mentioned above is given in Table 7. [Pg.351]

Control of the yields in the synthesis of alkyl peresters from the corresponding hydroperoxide and excess of acyl halide (equation 81) can be realized by RP-HPLC with DA-UVD or RID. The usual components of the analyte mixture are stable in the short retention times of the chromatographic runs (less than 4 min). The method was applied to control the synthesis of cumyl perbenzoate, perbutyrate and pervalerate. ... [Pg.700]

A number of alkylgennanium peroxides have been prepared by treating alkylgerma-nium halides with the appropriate alkyl hydroperoxide in the presence of base under anhydrous conditions (equations 103 and 104), or with the anhydrous sodium salt of the... [Pg.823]


See other pages where Hydroperoxides halides is mentioned: [Pg.886]    [Pg.168]    [Pg.630]    [Pg.492]    [Pg.493]    [Pg.795]    [Pg.257]    [Pg.144]    [Pg.31]    [Pg.53]    [Pg.187]    [Pg.307]    [Pg.310]    [Pg.315]    [Pg.327]    [Pg.328]   
See also in sourсe #XX -- [ Pg.12 , Pg.299 ]




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Alkyl halides, hydroperoxide synthesis

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