Concise synthesis of an enantiopure bicyclic pyrazinone as constrained peptidomimetic building block. - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Organic & Biomolecular Chemistry Année : 2012

Concise synthesis of an enantiopure bicyclic pyrazinone as constrained peptidomimetic building block.

Résumé

A concise synthetic route has been developed for the preparation of a constrained peptidomimetic pyrazinone building block. From hydroxy-L-lysine, the desired pyrazinone is obtained in 43% overall yield (6 steps) via an efficient deprotection-double cyclization sequence.

Domaines

Chimie organique
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Dates et versions

hal-00997078 , version 1 (27-05-2014)

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Citer

Vincent Gembus, Solenn Janvier, Jean-Pierre Lecouvé, Lucile Vaysse-Ludot, Jean-François Brière, et al.. Concise synthesis of an enantiopure bicyclic pyrazinone as constrained peptidomimetic building block.. Organic & Biomolecular Chemistry, 2012, 10 (10), pp.2003-2007. ⟨10.1039/c2ob06762e⟩. ⟨hal-00997078⟩
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