Pseudoenantiomeric oxetane delta-amino acid scaffolds derived from L-rhamnose and D-xylose: D/L-alanine-D-serine and glycine-L-serine dipeptide isosteres
A series of oxetane δ-amino acid scaffolds derived from L-rhamnose and D-xylose provide a new class of templated sugar amino acids (SAA), which can be considered as D/L-alanine-D-serine and glycine-L-serine dipeptide isosteres. © 2004 Elsevier Ltd. All rights reserved.
Main Authors: | Johnson, S, Jenkinson, S, Angus, D, Jones, J, Watkin, D, Fleet, G |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2004
|
Similar Items
-
The synthesis of oligomers of oxetane-based dipeptide isosteres derived from L-rhamnose or D-xylose.
by: Johnson, S, et al.
Published: (2005) -
Conformational studies of oligomeric oxetane-based dipeptide isosteres derived from L-rhamnose or D-xylose.
by: Johnson, S, et al.
Published: (2005) -
Cyclic oligomers of oxetane-based dipeptide isosteres derived from L-rhamnose
by: Fleet, G, et al.
Published: (2006) -
Cyclic oligomers of oxetane-based dipeptide isosteres derived from L-rhamnose.
by: Fleet, G, et al.
Published: (2006) -
Oxetane cis- and trans-beta-amino-acid scaffolds from L-rhamnose by efficient S(N)2 reactions in oxetane rings; pseudoenantiomeric analogues of the antibiotic oxetin
by: Johnson, S, et al.
Published: (2004)