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...
Autori principali: | Smith, M, Long, D, Marquess, D, Claridge, T, Fleet, G |
---|---|
Natura: | Journal article |
Lingua: | English |
Pubblicazione: |
1998
|
Documenti analoghi
-
A solid phase approach to oligomers of carbohydrate amino-acids: Secondary structure in a trimeric furanose carbopeptoid
di: Long, D, et al.
Pubblicazione: (1998) -
Furanose carbopeptoids: Synthesis and secondary structural characteristics of carbohydrate omega-amino and oligomers.
di: Smith, M, et al.
Pubblicazione: (1998) -
From sequencamers to foldamers? Tetrameric furanose carbopeptoids from cis- and trans-5-aminomethyl-tetrahydrofuran-2-carboxylates
di: Long, D, et al.
Pubblicazione: (1999) -
Synthesis of tetrahydrofuran templated beta- and gamma-amino acid carbopeptoids.
di: Watterson, M, et al.
Pubblicazione: (2000) -
An octameric carbopeptoid; Secondary structure in octameric and tetrameric 5-aminomethyl-tetrahydrofuran-2-carboxylates
di: Claridge, T, et al.
Pubblicazione: (1999)