Efficient synthesis of building blocks for branched rhamnogalacturonan I fragments
| Autor: | Hans-Ulrich Endress, Dirk Michalik, Andreas Gottwald, Amayak Pogosyan, Christian Vogel |
|---|---|
| Rok vydání: | 2013 |
| Předmět: |
Glycosylation
food.ingredient Pectin Stereochemistry Molecular Sequence Data Organic Chemistry Galactose Chemistry Techniques Synthetic General Medicine Biochemistry Acceptor Analytical Chemistry Structure-Activity Relationship chemistry.chemical_compound food Carbohydrate Sequence chemistry Bromide Yield (chemistry) Rhamnogalacturonan I Pectins |
| Zdroj: | Carbohydrate Research. 380:9-15 |
| ISSN: | 0008-6215 |
| Popis: | Starting from allyl 2-O-acetyl-3-O-benzyl-α-l-rhamnopyranoside (3), allyl (2,3,4,6-tetra-O-benzoyl-β-d-galactopyranosyl)-(1→4)-2-O-acetyl-3-O-benzyl-α-l-rhamnopyranoside (5) was synthesized under Helferich conditions. Module 5 was converted to 2,3,4,6-tetra-O-benzoyl-β-d-galactopyranosyl-(1→4)-2-O-acetyl-3-O-benzyl-α-l-rhamnopyranosyl bromide (8) which was then coupled with methyl (allyl 2,3-di-O-benzyl-β-d-galactopyranosid)uronate (11) to provide methyl (2,3,4,6-tetra-O-benzoyl-β-d-galactopyranosyl)-(1→4)-(2-O-acetyl-3-O-benzyl-α-l-rhamnopyranosyl)-(1→4)-(allyl 2,3-di-O-benzyl-β-d-galactopyranosid)uronate (14). Alternatively, module 5 was transformed into allyl 2,3,4,6-tetra-O-benzoyl-β-d-galactopyranosyl-(1→4)-3-O-benzyl-α-l-rhamnopyranoside (9) suitable as an acceptor for the glycosylation with methyl 4-O-acetyl-2,3-di-O-benzyl-α/β-d-galactopyranosyluronate N-phenyl trifluoroacetimidate (13) to yield allyl (methyl 4-O-acetyl-2,3-di-O-benzyl-α-d-galactopyranosyluronate)-(1→2)-[2,3,4,6-tetra-O-benzoyl-β-d-galactopyranosyl]-(1→4)-3-O-benzyl-α-l-rhamnopyranoside (15). Both trisaccharides modules are suitable for the synthesis of branched pectin fragments. |
| Databáze: | OpenAIRE |
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