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Article Dans Une Revue SYNLETT Année : 2000

Diastereoselective Pentadienylation Reaction of Protected Chiral α-Amino Aldehydes

Résumé

Diastereoselective pentadienylation of chiral alpha-amino aldehydes was achieved. The obtained anti amino alcohols can be transformed into dienic imines which undergo Diels-Alder cyclisation to give stereoselectively indolizidines.
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Dates et versions

hal-04331691 , version 1 (11-12-2023)

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Citer

Frédéric Minassian, Nadia Pelloux-Léon, Yannick Vallée. Diastereoselective Pentadienylation Reaction of Protected Chiral α-Amino Aldehydes. SYNLETT, 2000, 2000 (2), pp.242-244. ⟨10.1055/s-2000-6500⟩. ⟨hal-04331691⟩

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