- Abstract:
-
This article describes the efficient synthesis of the first generation of branched sugar amino acid (SAA) oligomers in solution phase via two main routes: by the use of a standard coupling reagent and via the use of active ester intermediates. Benzyl-protected dimeric carbopeptoid and methyl-protected dimeric and tetrameric, hexameric and octameric carbopeptoids were obtained from a branched δ-3,5-trans-tetrahydrofuran (THF) SAA and methyl-protected dimeric and tetrameric carbopeptoids were s...
Expand abstract - Publication status:
- Published
- Publisher copy:
- 10.1007/s00726-011-0849-7
-
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- Journal:
- Amino acids
- Volume:
- 41
- Issue:
- 3
- Pages:
- 643-661
- Publication date:
- 2011-08-05
- DOI:
- EISSN:
-
1438-2199
- ISSN:
-
0939-4451
- URN:
-
uuid:31f88bbf-4e2d-42d4-83b9-c153873063d6
- Source identifiers:
-
167669
- Local pid:
- pubs:167669
- Language:
- English
- Keywords:
- Copyright date:
- 2011
Journal article
C-3 branched δ-3,5-cis- and trans-THF sugar amino acids: synthesis of the first generation of branched homooligomers.
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