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3- piperidine 5-amino-1 -alkyne

Termination of cyclic carbopalladation of alkynes via caibonylative lactamization can be achieved more satisfactorily with alkenyl or aryl halides containing an oo-caiboxamido or co-sulfonamido group than with those containing an 0)-amino group. The method appears to be satisfactory for the preparation of certain piperidines (e.g., 102) <96T(52)11529>. [Pg.241]

See other pages where 3- piperidine 5-amino-1 -alkyne is mentioned: [Pg.140]    [Pg.340]    [Pg.443]    [Pg.2305]    [Pg.2420]    [Pg.2470]    [Pg.2572]    [Pg.1308]    [Pg.1923]    [Pg.188]    [Pg.294]   
See also in sourсe #XX -- [ Pg.664 ]



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Piperidine 1-amino

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