Peptide templated glycosylation reactions

Citation
Rj. Tennant-eyles et al., Peptide templated glycosylation reactions, TETRAHEDR-A, 11(1), 2000, pp. 231-243
Citations number
22
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON-ASYMMETRY
ISSN journal
09574166 → ACNP
Volume
11
Issue
1
Year of publication
2000
Pages
231 - 243
Database
ISI
SICI code
0957-4166(20000128)11:1<231:PTGR>2.0.ZU;2-E
Abstract
Glycosyl donors and accepters may be covalently linked to aspartic acid res idues via OH-6 esters. Peptide elaboration allows glycosylation reactions t o be performed between donors and accepters linked to this peptide template . These reactions display increased regio- and stereoselectivities, which a re dependent on the nature of the peptide. Simple molecular modelling is us ed to rationalise the differing product distributions obtained by variation of the linking amino acid sequence. (C) 2000 Elsevier Science Ltd. All rig hts reserved.