Synthesis of Protected Hexp-(1 → 4)-β-D-GlcpNAc-(1 → 2)-α-D-Manp-(1 → O)(CH2)7CH3 Sequences (Hex: β-D-Glc, 4-deoxy-4fluoro-β-D-Gal, or 4-deoxy-β-D-Gal) Using a Glc-GlcNPhth Donor, Eventually Fluorinated or Deoxygenated at the Oligosaccharide Level. -The title trisaccharide derivatives are prepared
Synthesis of β-D-Galp-(1→4)-β-D-GlcpNAc- (1→2)-α-D-Manp-(1→O) (CH2)7CH3 Mimics to Explore the Substrate Specificity of Sialyltransferases and trans-Sialidases.
✍ Scribed by John A. F. Joosten; Britta Evers; Ruben P. van Summeren; Johannis P. Kamerling; Johannes F. G. Vliegenthart
- Publisher
- John Wiley and Sons
- Year
- 2004
- Weight
- 57 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
2004 Carbohydrates Carbohydrates U 0500 Synthesis of β-D-Galp-(1→4)-β-D-GlcpNAc-(1→2)-α-D-Manp-(1→O)(CH 2 ) 7 CH 3 Mimics to Explore the Substrate Specificity of Sialyltransferases and trans-Sialidases. -(JOOSTEN,
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
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