Intramolecular nitrone cycloaddition: Stereoselective synthesis of piperidine systems

DOI: 10.1016/0040-4020(96)00883-6

Source and publish data:

Tetrahedron p. 14311 - 14322 (1996)

Update date:2022-07-29

Topics:

Authors:

Chiacchio, Ugo

Rescifina, Antonio

Casuscelli, Francesco

Piperno, Anna

Pisani, Vincenzo

Romeo, Roberto

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Article abstract of DOI:10.1016/0040-4020(96)00883-6

A synthetic approach to isomerically functionalized piperidine systems has been designed by intramolecular nitrone cycloaddition, starting from β-enamidoaldehydes, and by subsequent reductive ring-opening of the obtained fused δ-lactams.

Full text of DOI:10.1016/0040-4020(96)00883-6

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