@article{
 title = {Synthesis of the Bacteriocin Glycopeptide Sublancin 168 and S -Glycosylated Variants},
 type = {article},
 year = {2012},
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 pages = {1910-1913},
 volume = {14},
 websites = {https://pubs.acs.org/doi/10.1021/ol300557g},
 month = {4},
 day = {6},
 id = {3546f255-35f2-3e79-8b4b-ded8dec03123},
 created = {2020-12-17T05:29:52.786Z},
 file_attached = {false},
 profile_id = {a5a2ab6f-a8b5-3db6-97bc-618752ee4386},
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 last_modified = {2020-12-17T05:29:52.786Z},
 read = {false},
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 citation_key = {Hsieh2012},
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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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