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Beilstein J. Org. Chem. 2013, 9, 56–63, doi:10.3762/bjoc.9.7
Graphical Abstract
Figure 1: Azidosugars used in this study. The synthesis of the azidosugars 1–3 was modified from [47,48], compounds 4...
Scheme 1: Reaction conditions and reagents: (a) Ns-chloride (6.00 equiv), 2,4,6-collidine (12.0 equiv), CH2Cl2...
Scheme 2: Synthesis of spermine conjugates 20,21 and 24,25. 2-chlorotrityl chloride resin was used as a solid...
Scheme 3: Synthesis of hexaalkynyl peptoids 26 and 27 on solid supports.
Scheme 4: Synthesis of a hexa-glycosylated peptoid 28.