@article{
 title = {Synthesis of the bacteriocin glycopeptide sublancin 168 and S-glycosylated variants},
 type = {article},
 year = {2012},
 pages = {1910-1913},
 volume = {14},
 id = {0782aeb9-904a-31dc-bf32-5d68b28b7eb4},
 created = {2023-01-10T01:45:00.240Z},
 file_attached = {false},
 profile_id = {a5a2ab6f-a8b5-3db6-97bc-618752ee4386},
 group_id = {bc1ab1d4-9e57-37e6-9fb5-435fca0ee9d2},
 last_modified = {2023-01-10T01:45:00.240Z},
 read = {false},
 starred = {false},
 authored = {false},
 confirmed = {false},
 hidden = {false},
 private_publication = {false},
 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, Y.S.Y. and Wilkinson, B.L. and O'Connell, M.R. and MacKay, J.P. and Matthews, J.M. and Payne, R.J.},
 doi = {10.1021/ol300557g},
 journal = {Organic Letters},
 number = {7}
}

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