223479-99-0

Upstream product

• 20231-36-1 methyl 6-O-trityl-α-D-mannopyranoside 
• 617-04-9 (2R,3S,4S,5S,6S)-2-(hydroxymethyl)-6-methoxytetrahydro-2H-pyran-3,4,5-triol 
• 270920-56-4 methyl 2,3,4-tri-O-(4-methoxybenzyl)-6-O-triphenylmethyl-α-D-mannopyranoside 

Downstream Products

• 223480-02-2 methyl-6-O-carboxy-(N-(9-fluorenylmethoxycarbonyl)-L-aspartic-acid α-tert-butyl ester)-2,3,4-tri-O-4-methoxybenzyl-α-D-manno-pyranoside 

Relevant academic research and scientific papers

Peptide templated glycosylation reactions

Glycosyl donors and acceptors may be covalently linked to aspartic acid residues via OH-6 esters. Peptide elaboration allows glycosylation reactions to be performed between donors and acceptors linked to this peptide template. These reactions display increased regio- and stereoselectivities, which are dependent on the nature of the peptide. Simple molecular modelling is used to rationalise the differing product distributions obtained by variation of the linking amino acid sequence. Copyright (C) 2000 Elsevier Science Ltd.