1447464-36-9

Upstream product

• 4393-06-0 1-Phenyl-2-propen-1-ol 
• 260352-12-3 (E)-5-(4-chlorophenyl)-2,2-diphenylpent-4-enal 
• 1431561-40-8 (1E, 4E)-2,2-dimethyl-5-phenylpent-4-enal oxime 

Downstream Products

• 1431561-46-4 (E)-tert-butyl(tert-butoxycarbonyl)oxy(2,2-dimethyl-5-phenylpent-4-en-1-yl)carbamate 
• 1431561-64-6 (2-benzyl-4,4-dimethylpyrrolidin-1-yl)(4-nitrophenyl)methanone 
• 1447464-37-0 C₁₃H₁₉NO*C₂HF₃O₂ 
• 1431561-22-6 (S)-2-benzyl-4,4-dimethylpyrrolidin-1-yl 4-nitrobenzoate 

Relevant academic research and scientific papers

Enantioselective thiourea-catalyzed intramolecular cope-type hydroamination

Catalysis of Cope-type rearrangements of bis-homoallylic hydroxylamines is demonstrated using chiral thiourea derivatives. This formal intramolecular hydroamination reaction provides access to highly enantioenriched α-substituted pyrrolidine products and represents a complementary approach to metal-catalyzed methods.