Carbohydrate Research p. 185 - 204 (1981)
Update date:2022-09-26
Topics: Ring Opening Nucleophilic Displacements 2-substituted fortimicins 2-deoxy-1,2-epimino-2-epi-fortimicin B 2-O-(methylsulfonyl)fortimicin derivatives
Tadanier, Jack
Martin, Jerry R.
Nadzan, Alex M.
Johnson, Paulette
Holms, James
et al.
Opening of the aziridine ring of 2-deoxy-1,2-epimino-2-epi-fortimicin B (10) has been effected with both chloride and azide.The reactions are both stereo- and regiospecific and give 2-chloro-2-deoxyfortimicin B (2c) and 2-azido-2-deoxyfortimicin B (2d).Th
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Doi:10.1246/cl.1981.457
(1981)Doi:10.1016/j.bmcl.2005.07.052
(2005)Doi:10.1016/S0960-894X(02)01040-5
(2003)Doi:10.1016/j.tet.2004.08.003
(2004)Doi:10.1016/j.tetlet.2004.08.059
(2004)Doi:10.1002/hlca.19810640420
(1981)