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New access to chiral pyrrolidine and piperidine β-enamino ketones. Application to the enantioselective synthesis of (–)-hygroline

Corinne Vanucci‐Bacqué, Sandrine Calvet‐Vitale, Marie‐Claude Fargeau‐Bellassoued, G. LHOMMET

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Abstract

We report here a new access to chiral pyrrolidine and piperidine β-enamino ketones by condensation of (S)-phenylglycinol with ω-oxo alkynones.As an illustration of the synthetic potential of the target compounds, the total enantioselective synthesis of alkaloid (-)-hygroline was achieved.

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We report here a new access to chiral pyrrolidine and piperidine β-enamino ketones by condensation of (S)-phenylglycinol with ω-oxo alkynones.As an illustration of the synthetic potential of the target compounds, the total enantioselective synthesis of alkaloid (-)-hygroline was achieved.

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Available abstract

We report here a new access to chiral pyrrolidine and piperidine β-enamino ketones by condensation of (S)-phenylglycinol with ω-oxo alkynones.As an illustration of the synthetic potential of the target compounds, the total enantioselective synthesis of alkaloid (-)-hygroline was achieved.

Key concepts: Pyrrolidine, Piperidine, Enantioselective synthesis, Chemistry, Alkaloid, Condensation, Organic chemistry, Combinatorial chemistry

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New access to chiral pyrrolidine and piperidine β-enamino ketones. Application to the enantioselective synthesis of (–)-hygroline — Research Paper | ScholarLens