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1,3-dithiane haloalkane

Stabilized radicals are generated. A list of the main type of radical precursors used for selenium atom transfer is depicted in Fig. 1. Malonates [64, 66-73], -ketoesters [74, 75], malononitriles [76-79], haloalkanes [80], diphosphonate [81], glycolate derivatives [82, 83] and dithianes [84]. More substrates such as a-seleno-esters, -nitriles, -ketones and -sulfones can also be used, however, the efficiency of the process is reduced [68]. [Pg.97]

Stork reagent) 1,3-dithiane cleavage, 328-329 Iodoalkanes. See Haloalkanes Iodoetherification, 272, 326 Iodolactones. See Halolactones Ion-exchange resins. See Benzene, ethenyl- ... [Pg.212]

See other pages where 1,3-dithiane haloalkane is mentioned: [Pg.2084]    [Pg.2398]    [Pg.2084]    [Pg.2084]    [Pg.2398]    [Pg.2084]    [Pg.2398]    [Pg.2084]    [Pg.2084]    [Pg.2398]    [Pg.2398]    [Pg.2398]    [Pg.2398]    [Pg.323]    [Pg.2398]    [Pg.2398]    [Pg.2398]    [Pg.2503]    [Pg.1221]    [Pg.1221]    [Pg.1221]    [Pg.2556]    [Pg.2563]    [Pg.927]   
See also in sourсe #XX -- [ Pg.1452 ]



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