Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5267031 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
New C-glycosylated Nβ-protected aza-β3-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 β-dipeptides by elongation at the C- or the N-terminus establishing their ability to be incorporated in original glycosylated foldamers.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Manuel Andreini, Anne-Sophie Felten, Hoang-Trang Tran Thien, Claude Taillefumier, Nadia Pellegrini-Moïse, Yves Chapleur,