20446-16-6Relevant articles and documents
Reaction of deferoxamine with organic acid chlorides
Gorak
, p. 107 - 109 (2008/10/08)
Deferoxamine is acylated at the primary amino group by mono- and dibasic organic acid chlorides with formation of substituted amides according to the Schotten-Baumann reaction. The obtained derivatives of deferoxamine, like deferoxamine itself, form with iron(III) stable salts, which are of low toxicity, but do not possess the properties of reversible bonding of oxygen at the temperature of the human organism.