80926-69-8

Upstream product

• 425644-02-6 N-(2-nitrobenzenesulfonyl)-N'-(benzyloxycarbonyl)-1,4-diaminobutane 
• 62146-62-7 (4-aminobutyl)carbamic acid benzyl ester 
• 501-53-1 benzyl chloroformate 
• 116861-31-5 tert-butyl N-(3-chloropropyl)carbamate 
• 425644-03-7 N⁸-benzyloxycarbonyl-N¹-tert-butyloxycarbonyl-N⁴-(2-nitrobenzenesulfonyl)-spermidine 
• 153815-24-8 1-(tert-butyloxycarbonylamino)-3,3-diethoxypropane 
• 24424-99-5 di-tert-butyl dicarbonate 
• 58885-60-2 N-(tert-butoxycarbonyl)-3-aminopropanal 
• 153815-25-9 N⁸-benzyloxycarbonyl-N¹-tert-butoxycarbonylspermidine 

Downstream Products

• 138093-86-4 N^α-(benzyloxycarbonyl)-N^β-(tert-butoxycarbonyl)-N^β-methyl-L-α,β-diaminopropionylglycyl-N⁵,N⁸-bis(tert-butoxycarbonyl)spermidine 
• 85503-20-4 N,N-bis(tert-butoxycarbonyl)spermidine 

Relevant academic research and scientific papers

Total Synthesis and Biological Evaluation of Paenilamicins from the Honey Bee Pathogen Paenibacillus larvae

Paenilamicins are a group of complex polycationic peptide secondary metabolites with antibacterial and antifungal activities produced by the devastating honey bee brood pathogen Paenibacillus larvae causing the lethal brood disease American Foulbrood (AFB

An efficient synthesis of selectively functionalized spermidine

A method is described for the synthesis of selectively protected Boc, Fmoc or Z-spermidine derivatives. The starting spermidine, N8-benzyloxycarbonyl-N1-tert-butoxycarbonylspermidine is prepared using a reductive amination.