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Halogenhydrins, cyclic

Mild and rapid ether cleavage Halogenhydrins from cyclic ethers... [Pg.429]

Another type of epoxy oligomers are the cyclo-aliphatic ones, obtained by oxidation of cyclic diolefins with various peroxidic compounds (organic or inorganic hydroperoxides), hypochlorous acid, halogenhydrines and their derivatives, and oxygen or ozone. At present, the main industrial procedure for their production uses peracetic acid. In keeping with initial cycloolefin structure, diepoxides with different structures are produced, with the peculiarity that peroxidic oxygen is bound to the aliphatic cycle. [Pg.444]

Without additional reagents lyl-Alkoxyhalides from oxo eompounds s. U, 908 Halogenhydrins from oxido compounds s. A, 475 s. a. J. L. Bose, A. B. Foster, and R. W. Stephens, Soc. 1959, 3314 Reactions with carbamyl chloride Chlorourethans s. 11, 590 Chloroallophanates from allophanyl chloride s. 11, 591 Oxetane ring opening lodohydrins from cyclic ethers s. 12, 626 Tetrahydrofuran ring opening s. 11, 1 w.a.r. CO C(OR)Hal C C -> C(OH)CHal... [Pg.177]

See other pages where Halogenhydrins, cyclic is mentioned: [Pg.241]    [Pg.234]    [Pg.251]    [Pg.259]    [Pg.272]    [Pg.241]    [Pg.234]    [Pg.251]    [Pg.259]    [Pg.272]    [Pg.234]    [Pg.309]    [Pg.313]    [Pg.263]    [Pg.265]    [Pg.536]   


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1,2-Halogenhydrins

Halogenhydrins ethers, cyclic

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