3-azidotetrahydrofuran-2-carboxylates: monomers for five-ring templated beta-amino acid foldamers?
Four diastereomeric methyl 3-azidotetrahydrofuran-2-carboxylates were prepared from diacetone glucose as precursors for the synthesis of β-amino acid oligomers with secondary structure.
Główni autorzy: | Watterson, M, Pickering, L, Smith, M, Hudson, S, Marsh, P, Mordaunt, J, Watkin, D, Newman, C, Fleet, G |
---|---|
Format: | Journal article |
Język: | English |
Wydane: |
1999
|
Podobne zapisy
-
Synthesis of tetrahydrofuran templated beta- and gamma-amino acid carbopeptoids.
od: Watterson, M, i wsp.
Wydane: (2000) -
Templated scaffolds of cis- and trans-tetrahydrofuran gamma-amino acids: gamma-azido-beta-hydroxy-tetrahydrofuran-2-carboxylates from pentono-delta-lactones
od: Sanjayan, G, i wsp.
Wydane: (2003) -
Cis- and trans-3-Azido-oxetane-2-carboxylate scaffolds: hexamers of oxetane cis-beta-amino acids
od: Barker, S, i wsp.
Wydane: (2001) -
Branched tetrahydrofuran alpha,alpha-disubstituted-delta-sugar amino acid scaffolds from branched sugar lactones: a new family of foldamers?
od: Simone, M, i wsp.
Wydane: (2005) -
From sequencamers to foldamers? Tetrameric furanose carbopeptoids from cis- and trans-5-aminomethyl-tetrahydrofuran-2-carboxylates
od: Long, D, i wsp.
Wydane: (1999)