Stereoselective Synthesis of 3-Amino-3-deoxy-aldohexoses by Aldol Condensation of Tricarbonyliron-alpha-Aminodienone Complexes: Total Synthesis of Multiprotected Kanosamine - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Synthesis: Journal of Synthetic Organic Chemistry Année : 2011

Stereoselective Synthesis of 3-Amino-3-deoxy-aldohexoses by Aldol Condensation of Tricarbonyliron-alpha-Aminodienone Complexes: Total Synthesis of Multiprotected Kanosamine

Laurence Miesch
Tania Welsch
  • Fonction : Auteur
Loic Toupet

Résumé

An aldol reaction between the divalent tin enol ether of racemic N-Boc alpha-aminodienone-tricarbonyliron complex and multiprotected D-glyceraldehyde provided predominantly two enantiomerically pure ketol diastereoisomers. From there, multiprotected kanosamine and 3-amino-3-deoxy-D-altrose were obtained in a few high-yielding steps, namely stereoselective reduction, protection, decomplexation, and ozonolysis.
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Dates et versions

hal-01068821 , version 1 (26-09-2014)

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Laurence Miesch, Tania Welsch, Loic Toupet. Stereoselective Synthesis of 3-Amino-3-deoxy-aldohexoses by Aldol Condensation of Tricarbonyliron-alpha-Aminodienone Complexes: Total Synthesis of Multiprotected Kanosamine. Synthesis: Journal of Synthetic Organic Chemistry, 2011, 1, pp.161-167. ⟨10.1055/s-0030-1258320⟩. ⟨hal-01068821⟩
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