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Article Dans Une Revue Tetrahedron Letters Année : 2012

Synthesis of new C-glycosyl aza-beta3-amino acids building blocks

Résumé

New C-glycosylated Nb-protected aza-beta3-amino acid building blocks have been prepared from C-glycosyl aldehydes of gluco and galacto configuration by reductive amination and subsequent N-alkylation. These moieties were elaborated to b-dipeptides by elongation at the C- or the N-terminus establishing their ability to be incorporated in original glycosylated foldamers.

Domaines

Chimie

Dates et versions

hal-00717767 , version 1 (13-07-2012)

Identifiants

Citer

Manuel Andreini, Anne-Sophie Felten, Hoang-Trang Tran Thien, Claude Taillefumier, Nadia Pellegrini-Moïse, et al.. Synthesis of new C-glycosyl aza-beta3-amino acids building blocks. Tetrahedron Letters, 2012, 53, pp.2702-2705. ⟨10.1016/j.tetlet.2012.03.072⟩. ⟨hal-00717767⟩
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