Synthesis of oligomers of tetrahydrofuran amino acids: furanose carbopeptoids
An acid catalysed ring rearrangement of a triflate derivative of D-mannono-γ-lactone 6 is the key step in the synthesis of the C-glycosyl sugar amino acid derivatives 3 and 4, examples of carbohydrate amino acid building blocks with specific conformational preferences suitable for incorporation into...
Hlavní autoři: | Smith, M, Long, D, Marquess, D, Claridge, T, Fleet, G |
---|---|
Médium: | Journal article |
Jazyk: | English |
Vydáno: |
1998
|
Podobné jednotky
-
A solid phase approach to oligomers of carbohydrate amino-acids: Secondary structure in a trimeric furanose carbopeptoid
Autor: Long, D, a další
Vydáno: (1998) -
Furanose carbopeptoids: Synthesis and secondary structural characteristics of carbohydrate omega-amino and oligomers.
Autor: Smith, M, a další
Vydáno: (1998) -
From sequencamers to foldamers? Tetrameric furanose carbopeptoids from cis- and trans-5-aminomethyl-tetrahydrofuran-2-carboxylates
Autor: Long, D, a další
Vydáno: (1999) -
Synthesis of tetrahydrofuran templated beta- and gamma-amino acid carbopeptoids.
Autor: Watterson, M, a další
Vydáno: (2000) -
An octameric carbopeptoid; Secondary structure in octameric and tetrameric 5-aminomethyl-tetrahydrofuran-2-carboxylates
Autor: Claridge, T, a další
Vydáno: (1999)