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Linear hydroformylation of N-protected allyl- or homoallylamines (cyclohydrocarbonylation: CHC), followed by a reductive amination constitute the two key steps toward convenient routes to aza-heterocycles. © 2010 American Chemical Society.

Airiau, E., Girard, N., Pizzetti, M., Salvadori, J., Taddei, M., Mann, A. (2010). Hydroformylation of Alkenylamines: Concise Approaches toward Piperidines, Quinolizidines, and Related Alkaloids. JOURNAL OF ORGANIC CHEMISTRY, 75(24), 8670-8673 [10.1021/jo101776y].

Hydroformylation of Alkenylamines: Concise Approaches toward Piperidines, Quinolizidines, and Related Alkaloids

Pizzetti, Marianna;Salvadori, Jessica;Taddei, Maurizio;
2010-01-01

Abstract

Linear hydroformylation of N-protected allyl- or homoallylamines (cyclohydrocarbonylation: CHC), followed by a reductive amination constitute the two key steps toward convenient routes to aza-heterocycles. © 2010 American Chemical Society.
2010
JOURNAL OF ORGANIC CHEMISTRY
Airiau, E., Girard, N., Pizzetti, M., Salvadori, J., Taddei, M., Mann, A. (2010). Hydroformylation of Alkenylamines: Concise Approaches toward Piperidines, Quinolizidines, and Related Alkaloids. JOURNAL OF ORGANIC CHEMISTRY, 75(24), 8670-8673 [10.1021/jo101776y].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/8986
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