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Hydrogen halides, reaction with epoxide

The hydrogenolyaia of cyclopropane rings (C—C bond cleavage) has been described on p, 105. In syntheses of complex molecules reductive cleavage of alcohols, epoxides, and enol ethers of 5-keto esters are the most important examples, and some selectivity rules will be given. Primary alcohols are converted into tosylates much faster than secondary alcohols. The tosylate group is substituted by hydrogen upon treatment with LiAlH (W. Zorbach, 1961). Epoxides are also easily opened by LiAlH. The hydride ion attacks the less hindered carbon atom of the epoxide (H.B. Henhest, 1956). The reduction of sterically hindered enol ethers of 9-keto esters with lithium in ammonia leads to the a,/S-unsaturated ester and subsequently to the saturated ester in reasonable yields (R.M. Coates, 1970). Tributyltin hydride reduces halides to hydrocarbons stereoselectively in a free-radical chain reaction (L.W. Menapace, 1964) and reacts only slowly with C 0 and C—C double bonds (W.T. Brady, 1970 H.G. Kuivila, 1968). [Pg.114]

In the following procedure, use is made of the basic character of epoxides. In the presence of phosphonium salts, ethylene oxide removes hydrogen halide and the alkylidenetriphenylphosphorane is produced. If a suitable carbonyl compound is present in the reaction mixture, its reaction with the in situ generated phosphorane proceeds readily to give the Wittig product. [Pg.107]

When simple aliphatic epoxides such as methyloxirane react with hydrogen halides, the dominant mode of reaction introduces halide at the less substituted primary carbon.88... [Pg.775]

Finally, a mention should be made about the one peroxo system which will become more and more dominant the organometallic oxides of rhenium(VII). Such compounds have been found to be of outstanding catalytic activity for a number of oxygen transfer reactions with hydrogen peroxide.92 The best studied complex is methyltrioxorhenium(VII) (MTO) and its congeners. Figure 2.32 illustrates its synthesis. Epoxidation, aromatic oxidation and halide oxidation with these complexes have been studied with hydrogen peroxide and shown to be remarkably efficacious. [Pg.57]


See other pages where Hydrogen halides, reaction with epoxide is mentioned: [Pg.434]    [Pg.41]    [Pg.119]    [Pg.612]    [Pg.13]    [Pg.225]    [Pg.162]    [Pg.114]    [Pg.391]    [Pg.391]    [Pg.403]    [Pg.601]    [Pg.230]    [Pg.147]    [Pg.1081]    [Pg.391]    [Pg.612]    [Pg.188]    [Pg.144]    [Pg.8]    [Pg.47]    [Pg.48]    [Pg.49]    [Pg.49]    [Pg.50]    [Pg.50]    [Pg.51]    [Pg.51]    [Pg.52]    [Pg.52]    [Pg.53]    [Pg.53]    [Pg.54]    [Pg.54]    [Pg.55]    [Pg.55]    [Pg.56]    [Pg.56]   
See also in sourсe #XX -- [ Pg.121 ]




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1,2-Epoxides, hydrogenation

Epoxidation reactions, with

Epoxide reaction

Epoxides halides

Epoxides reactions

Hydrogen epoxidation

Hydrogen epoxidation with

Hydrogen halides

Hydrogen halides epoxides

Hydrogen halides reactions

Hydrogen halides with epoxides

Hydrogenation reaction with

Hydrogenation, halides

Reaction with epoxides

Reaction with hydrogen

Reactions epoxidation

With epoxides

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