260997-37-3

Upstream product

• 6325-93-5 p-nitrobenzenesulfonamide 
• 459-57-4 4-fluorobenzaldehyde 

Downstream Products

• 1217270-45-5 N-(4-nitrobenzenesulfonyl)-3-(4-fluorophenyl)-oxaziridine 
• 1005774-50-4 C₂₁H₂₂N₂O₅S 
• 1194759-17-5 C₂₇H₁₉FN₂O₅S 
• 1145782-02-0 (R)-4-(4-fluorophenyl)-1-p-nitrobenzenesulfonyl-3,3-triphenylazetidin-2-one 
• 1145782-01-9 (3S,4R)-4-(4-fluorophenyl)-3-methyl-1-p-nitrobenzenesulfonyl-3-phenylazetidin-2-one 
• 1145782-00-8 (3R,4R)-4-(4-fluorophenyl)-3-methyl-1-p-nitrobenzenesulfonyl-3-phenylazetidin-2-one 
• 1145781-95-8 (3S,4R)-3-ethyl-4-(4-fluorophenyl)-1-p-nitrobenzenesulfonyl-3-phenylazetidin-2-one 
• 1145781-94-7 (3R,4R)-3-ethyl-4-(4-fluorophenyl)-1-p-nitrobenzenesulfonyl-3-phenylazetidin-2-one 

Relevant academic research and scientific papers

Carbonyl Imines from oxaziridines: Generation and cycloaddition of N-O=C dipoles

Dipoles apart: Unusual 1,3-dipolar carbonyl imines are generated in the presence of a bulky scandium(III) catalyst by undergoing a Lewis acid catalyzed rearrangement of N-sulfonyl oxaziridines. The 1,3-dipolar carbonyl imines then undergo subsequent cyclo