A novel synthesis of gamma-lactam derivatives 4 is reported, based on PdI2-catalyzed oxidative monoaminocarbonylation of 2-ynylamines, followed by in situ conjugate addition of a secondary amine and lactamization. Tetramic acids can be easily obtained from 4 by acid-catalyzed hydrolysis at room temperature.

A new synthesis of 4-dialkylamino-1,5-dihydropyrrol-2-ones by Pd-catalyzed oxidative Aminocarbonylation of 2-Ynylamines

Gabriele B.;Plastina P.;
2005-01-01

Abstract

A novel synthesis of gamma-lactam derivatives 4 is reported, based on PdI2-catalyzed oxidative monoaminocarbonylation of 2-ynylamines, followed by in situ conjugate addition of a secondary amine and lactamization. Tetramic acids can be easily obtained from 4 by acid-catalyzed hydrolysis at room temperature.
2005
Aminocarbonylation ; Carbonylation; gamma-Lactams; Palladium ; Tetramic Acids; Heterocycles
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11770/123622
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