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Alkenes organoboron compounds

Addition of dialkyl aluminum hydrides (dialkyl alanes) to C=C double bonds in alkenes (hydroalumination) leads to trialkyl alanes (291, 298). For the preparation of higher trialkyl alanes it is proposed to add diethyl-alane to higher 1-alkenes and from the resulting ethyl-alkyl alane mixtures (analogous to the organoboron compounds) (142) to remove the ethyl groups as triethylalane by distillation (241) ... [Pg.311]

The alkyl- or alkenyl-organoboron compound used in a Suzuki reaction is prepared by hydroboration of a terminal alkene or a terminal alkyne, respectively. Often the boron-contairting compound is catecholborane. [Pg.544]


See other pages where Alkenes organoboron compounds is mentioned: [Pg.323]    [Pg.300]    [Pg.328]    [Pg.327]    [Pg.118]    [Pg.245]    [Pg.712]    [Pg.533]    [Pg.212]    [Pg.69]    [Pg.481]    [Pg.10]    [Pg.448]    [Pg.345]    [Pg.348]    [Pg.480]    [Pg.484]    [Pg.309]    [Pg.56]    [Pg.265]    [Pg.182]    [Pg.139]    [Pg.295]    [Pg.645]    [Pg.461]    [Pg.101]    [Pg.29]    [Pg.351]    [Pg.139]    [Pg.276]    [Pg.617]    [Pg.164]    [Pg.165]    [Pg.39]    [Pg.3]    [Pg.21]    [Pg.295]   
See also in sourсe #XX -- [ Pg.144 , Pg.145 , Pg.146 , Pg.147 ]

See also in sourсe #XX -- [ Pg.4 , Pg.144 , Pg.145 , Pg.146 , Pg.147 ]




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