2'-N-ACYLFORTIMICINS AND 2'-N-ALKYLFORTIMICINS via THE ISOFORTIMICIN REARRANGEMENT

DOI: 10.1016/S0008-6215(00)84564-4

Source and publish data:

Carbohydrate Research p. 61 - 72 (1980)

Update date:2022-07-29

Topics: Reaction Mechanism Derivative Synthesis

Authors:

Tadanier, Jack

Martin, Jerry R.

Johnson, Paulette

Goldstein, Alma W.

Hallas, Robert

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Article abstract of DOI:10.1016/S0008-6215(00)84564-4

Fortimicin A and a number of 4-N-acylfortimicins B, although stable as either the fully protonated hydrochloride of sulfate salts, undergo degradation as the free bases in aqueous solution.Detailed studies with fortimicin A and 4-N-acetylfortimicin B have

Full text of DOI:10.1016/S0008-6215(00)84564-4

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