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Cyclooctane, carboxylation

C11H17N N-ethyl-alpha-methylbenzeneethanamine 457-87-4 515.00 46.000 2 22615 C11H1803 ethyl 2-0X0-1-cyclooctane carboxylate 4017-56-5 554.65 49.159 2... [Pg.507]

Alkylcyclohexanes, cycloheptane, and cyclooctane were also transformed into the esters of the corresponding tertiary cyclohexanecarboxylic acids in the presence of the superelectrophile CBr4—2AlBr3 in good yields.314 315 Such organic superacids generated from polyhalomethanes with aluminum halides are capable of promoting the selective and effective carboxylation of linear alkanes (propane, butane) and adamantane as well.316... [Pg.393]

See other pages where Cyclooctane, carboxylation is mentioned: [Pg.103]    [Pg.104]    [Pg.132]    [Pg.103]    [Pg.104]    [Pg.132]    [Pg.281]    [Pg.191]    [Pg.383]    [Pg.34]   
See also in sourсe #XX -- [ Pg.625 ]



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