210548-96-2

Upstream product

• 90914-08-2 N-[N-(tert-Butyloxycarbonyl)-3-aminopropyl]benzylamine 
• 90914-11-7 N-[N-(tert-Butoxycarbonyl)-3-aminopropyl]-N-(3-cyanopropyl)benzylamine 

Downstream Products

• 210548-97-3 (R)-3-{3-[Benzyl-(3-cyano-propyl)-amino]-propylamino}-3-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-propionic acid ethyl ester 
• 210549-10-3 (R)-9-Benzyl-4-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-oxo-1,5,9-triaza-cyclotridecane-1,5-dicarboxylic acid 5-benzyl ester 1-tert-butyl ester 
• 210549-13-6 (R)-9-Benzyl-4-((Z)-hept-1-enyl)-2-oxo-1,5,9-triaza-cyclotridecane-1,5-dicarboxylic acid 5-benzyl ester 1-tert-butyl ester 
• 210549-11-4 (R)-9-Benzyl-4-((S)-1,2-dihydroxy-ethyl)-2-oxo-1,5,9-triaza-cyclotridecane-1,5-dicarboxylic acid 5-benzyl ester 1-tert-butyl ester 
• 210549-12-5 (R)-9-Benzyl-4-formyl-2-oxo-1,5,9-triaza-cyclotridecane-1,5-dicarboxylic acid 5-benzyl ester 1-tert-butyl ester 
• 210549-09-0 (R)-1-Benzyl-6-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-8-oxo-1,5,9-triaza-cyclotridecane-5-carboxylic acid benzyl ester 
• 210549-14-7 (R)-1-Benzyl-6-((Z)-hept-1-enyl)-8-oxo-1,5,9-triaza-cyclotridecane-5-carboxylic acid benzyl ester 
• 210549-03-4 (R)-1-Benzyl-6-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-8-oxo-1,5,9-triaza-cyclotridecane-5-carboxylic acid tert-butyl ester 
• 210549-15-8 (R)-4-((Z)-Hept-1-enyl)-2-oxo-1,5,9-triaza-cyclotridecane-5-carboxylic acid benzyl ester 
• 210549-04-5 (R)-1-Benzyl-6-((S)-1,2-dihydroxy-ethyl)-8-oxo-1,5,9-triaza-cyclotridecane-5-carboxylic acid tert-butyl ester 
• 210548-98-4 (R)-3-{3-[(4-Amino-butyl)-benzyl-amino]-propylamino}-3-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-propionic acid ethyl ester 
• 210548-99-5 (3R,4'S)-12-amino-8-benzyl-3-(2',2'-dimethyldioxolan-4'-yl)-4,8-diazadodecanoic acid 
• 210549-06-7 (R)-1-Benzyl-6-chloromethyl-8-oxo-1,5,9-triaza-cyclotridecane-5-carboxylic acid tert-butyl ester 
• 210549-05-6 (R)-1-Benzyl-6-hydroxymethyl-8-oxo-1,5,9-triaza-cyclotridecane-5-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

Synthesis of the Spermidine Alkaloid ( - )-(4R)-Dihydroisomyricoidine

An asymmetric synthesis of (-)-(4R)-dihydroisomyricoidine (28), a 13-membered amino lactam of type A, was performed by a diastereoselective Michael addition between the spermidine derivative 3 and the commercially available optically active ethyl carboxyl