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Pyrrolidinium salts hydrogenation

Scheme 6.15 Ruthenium catalyzed asymmetric hydrogenation of pyrrolidinium salts. Scheme 6.15 Ruthenium catalyzed asymmetric hydrogenation of pyrrolidinium salts.
Diazomethane reacts with the salts of enamines to yield aziridinium salts.327 327a ThusiV-cyclohexylidenepyrrolidinium perchlorate yields 2,2 -pentamethylene-1,1 -tetramet hyleneaziridinium perchlorate (101). Hydrogenation over Adams catalyst cleaves the bond between the quaternary nitrogen atom and the methylene group to form A-(l-methylcyclohexyl)pyrrolidinium perchlorate (102). [Pg.213]

See other pages where Pyrrolidinium salts hydrogenation is mentioned: [Pg.27]    [Pg.212]    [Pg.22]    [Pg.132]    [Pg.255]    [Pg.619]    [Pg.522]    [Pg.138]    [Pg.6]    [Pg.59]    [Pg.76]   
See also in sourсe #XX -- [ Pg.212 ]



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Pyrrolidinium

Pyrrolidinium salts

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