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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
 
 
 
 

Regioselective glycosylation of neamine core: a facile entry to kanamycin B related analogues.

[reaction: see text] Introduction of a sugar unit at either the O5 or O6 position of various neamine derivatives in excellent selectivity and yields is described here. Application to the synthesis of kanamycin analogues is also highlighted.[1]

References

  1. Regioselective glycosylation of neamine core: a facile entry to kanamycin B related analogues. Chou, C.H., Wu, C.S., Chen, C.H., Lu, L.D., Kulkarni, S.S., Wong, C.H., Hung, S.C. Org. Lett. (2004) [Pubmed]
 
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