22147-83-7

Upstream product

• 1569095-70-0 (2E)-N-methoxy-N-((1S)-1-phenylprop-2-en-1-yl)but-2-enamide 
• 1569095-79-9 (5S)-1-methoxy-5-phenylpyrrolidin-2-one 
• 100-58-3 phenylmagnesium bromide 
• 1569096-23-6 (5S)-1-methoxy-5-phenylpyrrolidin-2-one-d3 
• 87802-71-9 (E)-methyl cinnamyl carbonate 
• 1569096-41-8 tert-butyl methoxy[(1S)-1-phenylprop-2-en-1-yl]carbamate-d3 
• 1569095-73-3 C₁₁H₁₁NO₂ 

Relevant academic research and scientific papers

Addition of organometallic reagents to chiral N-methoxylactams: Enantioselective syntheses of pyrrolidines and piperidines

Enantioselective iridium-catalyzed allylic substitutions were used to prepare N-allyl hydroxamic acid derivatives that were suitable for ring-closing metathesis, giving N-methoxylactams. Reactions of these derivatives with Grignard or organolithium compou