An Efficient Modular Approach for the Assembly of S-Linked Glycopeptoids
- 5 August 2009
- journal article
- research article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 11 (17) , 3898-3901
Abstract
A short and convenient methodology for the synthesis of S-glycosylated peptoid models is described. The thioglycosylated building blocks were prepared from proper peracetylated sugars via glycosyl iodides in a one-pot fashion and directly employed in a submonomer solid-phase stategy.Keywords
This publication has 40 references indexed in Scilit:
- Glycoprotein Synthesis: An UpdateChemical Reviews, 2008
- Peptoid architectures: elaboration, actuation, and applicationCurrent Opinion in Chemical Biology, 2008
- Cyclic β-PeptoidsOrganic Letters, 2008
- Strong inhibition of cholera toxin binding by galactose dendrimersChemical Communications, 2007
- Pentamer is the minimum structure for oligomannosylpeptoids to bind to concanavalin ABioorganic & Medicinal Chemistry Letters, 2007
- Novel Approaches for the Synthesis and Activation of Thio- and Selenoglycoside DonorsThe Journal of Organic Chemistry, 2007
- A General Strategy toward S‐Linked GlycopeptidesAngewandte Chemie International Edition, 2005
- An NDPase links ADAM protease glycosylation with organ morphogenesis in C. elegansNature Cell Biology, 2003
- Synthesis of S-Linked Glycopeptides in Aqueous SolutionThe Journal of Organic Chemistry, 2003
- Intracellular Functions of N-Linked GlycansScience, 2001