Synthesis of the Bacteriocin Glycopeptide Sublancin 168 and S -Glycosylated Variants. Hsieh, Y., S., Y., Wilkinson, B., L., O’Connell, M., R., Mackay, J., P., Matthews, J., M., & Payne, R., J. Organic Letters, 14(7):1910-1913, 4, 2012.
Synthesis of the Bacteriocin Glycopeptide Sublancin 168 and S -Glycosylated Variants [link]Website  abstract   bibtex   
The synthesis of sublancin 168, a unique S-glucosylated bacteriocin antibiotic, is described. The natural product and two S-glycosylated variants were successfully prepared via native chemical ligation followed by folding. The synthetic glycopeptides were shown to possess primarily an α-helical secondary structure by CD and NMR studies. © 2012 American Chemical Society.
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 title = {Synthesis of the Bacteriocin Glycopeptide Sublancin 168 and S -Glycosylated Variants},
 type = {article},
 year = {2012},
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 pages = {1910-1913},
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 websites = {https://pubs.acs.org/doi/10.1021/ol300557g},
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 abstract = {The synthesis of sublancin 168, a unique S-glucosylated bacteriocin antibiotic, is described. The natural product and two S-glycosylated variants were successfully prepared via native chemical ligation followed by folding. The synthetic glycopeptides were shown to possess primarily an α-helical secondary structure by CD and NMR studies. © 2012 American Chemical Society.},
 bibtype = {article},
 author = {Hsieh, Yves S. Y. and Wilkinson, Brendan L. and O’Connell, Mitchell R. and Mackay, Joel P. and Matthews, Jacqueline M. and Payne, Richard J.},
 journal = {Organic Letters},
 number = {7}
}

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