1420479-75-9

Upstream product

• 1420479-36-2 (Z)-3-nitro-N-(4-phenylhex-4-en-1-yl)benzenesulfonamide 
• 1420479-57-7 (S)-2-((S)-1-bromoethyl)-1-((3-nitrophenyl)sulfonyl)-2-phenylpyrrolidine 
• 1420480-27-8 C₁₃H₁₈O₃S 
• 1420480-10-9 (Z)-4-phenylhex-4-en-1-ol 
• 90173-08-3 (Z)-4-Phenyl-hex-4-enoic acid methyl ester 

Downstream Products

• 1420479-76-0 (R)-6-methyl-1-((3-nitrophenyl)sulfonyl)-5-phenyl-1,2,3,6-tetrahydropyridine 

Relevant academic research and scientific papers

C2-symmetric cyclic selenium-catalyzed enantioselective bromoaminocyclization

A catalytic asymmetric bromocyclization of trisubstituted olefinic amides that uses a C2-symmetric mannitol-derived cyclic selenium catalyst and a stoichiometric amount of N-bromophthalimide is reported. The resulting enantioenriched pyrrolidine products, which contain two stereogenic centers, can undergo rearrangement to yield 2,3-disubstituted piperidines with excellent diastereoselectivity and enantiospecificity.