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Skeletal rearrangement, 2,2-dimethylbutane

If methylpentanes and dimethylbutanes are able to give C5 or Cg cyclic products, this must involve some sort of skeletal rearrangement. Aromatiza-... [Pg.298]

Surprisingly, gold can also catalyze skeletal rearrangements of hydrocarbons for instance, the isomerization of 2,2-dimethylbutane to n-hexane has been achieved by Schmid with the aid of AU55 clusters on titanium dioxide [4c, 6] and the aromatization of the dispirocycle 1 to tetrahydronaphthalene 2 was achieved by de Meijere et al. in a reactor with gold surface at 100 °C in a few seconds (Scheme 1) [7]. [Pg.48]


See other pages where Skeletal rearrangement, 2,2-dimethylbutane is mentioned: [Pg.91]    [Pg.531]    [Pg.59]    [Pg.34]    [Pg.14]    [Pg.53]    [Pg.184]   
See also in sourсe #XX -- [ Pg.37 , Pg.59 ]




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Skeletal rearrangement

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