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Article Dans Une Revue Tetrahedron Letters Année : 2010

Straightforward synthesis of indolizidine alkaloid 167B

Résumé

The synthetic access to indolizidines, substituted in C-5 position, was reported with good diastereoselectivity. The strategy developed was based on a key step of Michael addition associated with a Clauson-Kaas condensation.

Domaines

Chimie organique
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Dates et versions

hal-01167326 , version 1 (24-06-2015)

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  • HAL Id : hal-01167326 , version 1

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Stéphanie Gracia, Rudolf Jerpan, S Pellet-Rostaing, Florence Popowycz, Marc Lemaire. Straightforward synthesis of indolizidine alkaloid 167B. Tetrahedron Letters, 2010, 51 (48), pp.6290-6293. ⟨hal-01167326⟩
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