647028-89-5

Upstream product

• 647028-82-8 2-[(2S,3R)-3-allyloxymethyl-1-trityl-aziridin-2-yl]-5-[(1R)-3-tert-butyldimethylsilyloxy-1-methylpropyl]oxazole 
• 647028-86-2 (2S,3R)-2-(5-[3-tert-butyldimethylsilyloxy-1-methylpropyl]oxazol-2-yl)-3-hydroxymethyl-1-tritylaziridine 
• 647028-81-7 5-[3-(tert-butyldimethylsilyloxy)-1-methylpropyl]oxazole 
• 647028-54-4 4-(tert-butyldimethylsilyloxy)-2-methylbutyric acid methyl ester 
• 285556-76-5 O-allyl-N-trityl-L-serinal 
• 647028-80-6 (S)-methyl 3-(allyloxy)-2-(tritylamino)propanoate 
• 13515-76-9 methyl N-trityl-L-serinate 
• 647028-87-3 (2S,3R)-2-(5-[3-tert-butyldimethylsilyloxy-1-methylpropyl]oxazol-2-yl)-3-iodomethyl-1-tritylaziridine 

Downstream Products

• 647028-92-0 (2S,3R)-2-[5-[3-acetoxy-6-tert-butyldimethylsilyloxy-1-methyl-4-hexynyl]oxazol-2-yl]-3-iodomethyl-1-tritylaziridine 
• 647028-77-1 (2S,3R)-3-iodomethyl-2-(5-[1-methyl-3-oxopropyl]oxazol-2-yl)-1-tritylaziridine 

Relevant academic research and scientific papers

Synthetic Enantiopure Aziridinomitosenes: Preparation, Reactivity, and DNA Alkylation Studies

An enantiocontrolled route to aziridinomitosenes had been developed from L-serine methyl ester hydrochloride. The tetracyclic target ring system was assembled by an internal azomethine ylide cycloaddition reaction based on silver ion-assisted intramolecul