647028-95-3

Upstream product

• 76782-82-6 tert-Butyldimethyl(prop-2-ynyloxy)silane 
• 647028-56-6 (2S,3R)-3-iodomethyl-2-(3-oxopropyloxazol-2-yl)-1-tritylaziridine 
• 13515-76-9 methyl N-trityl-L-serinate 
• 647028-80-6 (S)-methyl 3-(allyloxy)-2-(tritylamino)propanoate 
• 285556-76-5 O-allyl-N-trityl-L-serinal 
• 285556-78-7 (2S,3R)-3-allyloxymethyl-2-[5-(3-tert-butyldimethylsilyloxypropyl)oxazol-2-yl]-1-tritylaziridine 
• 647028-88-4 (2S,3R)-2-(hydroxypropyloxazol-2-yl)-3-iodomethyl-1-tritylaziridine 
• 647028-85-1 (2S,3R)-2-(5-tert-butyldimethylsilyloxypropyloxazol-2-yl)-3-hydroxymethyl-1-tritylaziridine 
• 647028-55-5 (2S,3R)-2-(5-tert-butyldimethylsilyloxypropyloxazol-2-yl)-3-iodomethyl-1-tritylaziridine 

Downstream Products

• 647028-65-7 (2S,3R)-2-[5-[3-acetoxy-6-(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 

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