860795-48-8Relevant articles and documents
Tuning the regioselectivity of the staudinger reaction for the facile synthesis of kanamycin and neomycin class antibiotics with N-1 modification
Li, Jie,Chen, Hsiao-Nung,Chang, Huiwen,Wang, Jinhua,Chang, Cheng-Wei Tom
, p. 3061 - 3064 (2007/10/03)
(Chemical Equation Presented) A novel method for achieving the desired regioselective reduction of the N-1 azido group on a tetraazidoneamine has been developed that leads to the synthesis of both kanamycin and neomycin class antibiotics bearing N-1 modif