285556-76-5

Upstream product

• 13515-76-9 methyl N-trityl-L-serinate 
• 647028-80-6 (S)-methyl 3-(allyloxy)-2-(tritylamino)propanoate 

Downstream Products

• 647028-62-4 (2S,3R)-2-[5-[6-(N-tert-butyldimethylsilylcarbamoyloxy)-3-tert-butyldimethylsilyloxy-4-hexynyl]oxazol-2-yl]-3-iodomethyl-1-tritylaziridine 
• 647028-66-8 (2S,3R)-2-[5-[3,6-bis-(tert-butyldimethylsilyloxy)-4-hexynyl]oxazol-2-yl]-3-iodomethyl-1-tritylaziridine 
• 647028-92-0 (2S,3R)-2-[5-[3-acetoxy-6-tert-butyldimethylsilyloxy-1-methyl-4-hexynyl]oxazol-2-yl]-3-iodomethyl-1-tritylaziridine 
• 647028-65-7 (2S,3R)-2-[5-[3-acetoxy-6-(tert-butyldimethylsilyloxy)-4-hexynyl]oxazol-2-yl]-3-iodomethyl-1-tritylaziridine 
• 647028-95-3 (2S,3R)-2-[5-[6-(tert-butyldimethylsilyloxy)-3-hydroxy-4-hexynyl]oxazol-2-yl]-3-iodomethyl-1-tritylaziridine 
• 647028-91-9 Carbamic acid 4-hydroxy-6-[2-((2S,3R)-3-iodomethyl-1-trityl-aziridin-2-yl)-oxazol-5-yl]-hex-2-ynyl ester 
• 647028-82-8 2-[(2S,3R)-3-allyloxymethyl-1-trityl-aziridin-2-yl]-5-[(1R)-3-tert-butyldimethylsilyloxy-1-methylpropyl]oxazole 
• 647028-87-3 (2S,3R)-2-(5-[3-tert-butyldimethylsilyloxy-1-methylpropyl]oxazol-2-yl)-3-iodomethyl-1-tritylaziridine 
• 647028-90-8 4-Hydroxy-6-[2-((2S,3R)-3-iodomethyl-1-trityl-aziridin-2-yl)-oxazol-5-yl]-hex-2-ynoic acid methyl ester 
• 647028-55-5 (2S,3R)-2-(5-tert-butyldimethylsilyloxypropyloxazol-2-yl)-3-iodomethyl-1-tritylaziridine 
• 647028-85-1 (2S,3R)-2-(5-tert-butyldimethylsilyloxypropyloxazol-2-yl)-3-hydroxymethyl-1-tritylaziridine 
• 647028-86-2 (2S,3R)-2-(5-[3-tert-butyldimethylsilyloxy-1-methylpropyl]oxazol-2-yl)-3-hydroxymethyl-1-tritylaziridine 
• 647028-89-5 (2S,3R)-2-(5-[3-hydroxy-1-methylpropyl]oxazol-2-yl)-3-iodomethyl-1-tritylaziridine 
• 647028-88-4 (2S,3R)-2-(hydroxypropyloxazol-2-yl)-3-iodomethyl-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