97222-24-7

Upstream product

• 6404-29-1 6-(tert-butoxycarbonylamino)hexanoic acid 
• 97222-22-5 Boc-Ahe-(BzlO)Apr-Ahe-(BzlO)Apr-OMe 
• 97222-21-4 H-(BzlO)Apr-Ahe-(BzlO)Apr-OMe 
• 97222-19-0 Boc-Ahe-(BzlO)Apr-OMe 
• 30204-31-0 3-(benzyloxyamino)propanoic acid methyl ester 

Downstream Products

• 97222-26-9 Boc-Ahe-(BzlO)Apr-Ahe-(BzlO)Apr-Ahe-(BzlO)Apr-OH 
• 97222-27-0 5,16,27-Tris-benzyloxy-1,5,12,16,23,27-hexaaza-cyclotritriacontane-2,6,13,17,24,28-hexaone 
• 97222-30-5 3-[Benzyloxy-(6-{3-[benzyloxy-(6-{3-[benzyloxy-(6-tert-butoxycarbonylamino-hexanoyl)-amino]-propionylamino}-hexanoyl)-amino]-propionylamino}-hexanoyl)-amino]-propionic acid 2,5-dioxo-pyrrolidin-1-yl ester 
• 97222-25-8 Boc-Ahe-(BzlO)Apr-Ahe-(BzlO)Apr-Ahe-(BzlO)Apr-OMe 

Relevant academic research and scientific papers

Synthesis of Linear and Cyclic Trihydroxamic Acids as Models for Ferrioxamines E and G

Linear and cyclic trihydroxamic acids including the 6-aminohexanoyl-3-(hydroxyamino)propanoyl sequence have been synthesized in a stepwise manner from the appropriately protected acyl derivatives and used as iron(III) chelating compounds.