## 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, please click on HTML or PDF.
Synthesis of neoglycopeptides by chemoselective reaction of carbohydrates with peptides containing a novel N′-methyl-aminooxy amino acid
✍ Scribed by Michael R Carrasco; Michael J Nguyen; Dawn R Burnell; Michael D MacLaren; Shawna M Hengel
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 89 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A novel N%-methyl-aminooxy amino acid has been designed, synthesized, and successfully incorporated into peptides using standard solid-phase peptide synthesis procedures. Reaction of these peptides with native reducing sugars yields neoglycopeptides via a chemoselective reaction with the aminooxy side chains. The key feature of the new amino acid is that it maintains attached sugars in their cyclic conformations and close to the peptide backbone.
📜 SIMILAR VOLUMES
## Abstract magnified image An approach to indole derivatives from __N__‐arylhydroxamic acids and malononitrile __via__ a [3,3]‐sigmatropic rearrangement and intramolecular cyclization is described. Reactions of __N__‐arylhydroxamic acids **1a‐c, 2a‐c** and **3a‐c** with malononitrile in the prese