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4-Methyl-/rans-2-pentene

Most of the experiments with 1-hexene were run to assess the effect of conditions of activation upon the rate of hydrogenation. We ran some experiments with Chemical Samples Company, Columbus, Ohio. The 4-methyl-1-pentene could be used directly but poisons in the /raws-2-hexene required it to be percolated through alumina directly into the saturator. [Pg.36]

The symmetrical 3-isopropenyl-4-methyl-4-penten-l-al with neutral [RhCl-(R)-BINAP] gives 3-isopropenyl-4-methylcyclopentanone preferentially as the d.v-isomer with > 99% ee, while the cationic complex leads to the /rans-isomer with > 99% ee52. [Pg.369]


See other pages where 4-Methyl-/rans-2-pentene is mentioned: [Pg.488]    [Pg.820]    [Pg.480]    [Pg.812]    [Pg.883]    [Pg.467]    [Pg.795]    [Pg.524]    [Pg.892]    [Pg.480]    [Pg.812]    [Pg.270]    [Pg.364]    [Pg.333]    [Pg.473]    [Pg.56]    [Pg.286]    [Pg.488]    [Pg.488]    [Pg.820]    [Pg.820]    [Pg.480]    [Pg.480]    [Pg.812]    [Pg.812]    [Pg.883]    [Pg.883]    [Pg.119]    [Pg.378]    [Pg.467]    [Pg.467]    [Pg.795]    [Pg.795]    [Pg.524]    [Pg.524]    [Pg.892]    [Pg.892]    [Pg.480]    [Pg.480]    [Pg.812]    [Pg.812]    [Pg.294]   
See also in sourсe #XX -- [ Pg.239 ]




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4- Methyl-2-pentene

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