1304540-30-4

Upstream product

• 1304540-32-6 (+)-N-{(1'S)-1-[(benzyloxy)methyl]prop-2-en-1-yl}-N-methoxybut-3-enamide 
• 1304540-10-0 (+)-tert-butyl {(1S)-1-[(benzyloxy)methyl]prop-2-en-1-yl}methoxycarbamate 

Downstream Products

• 1304540-38-2 (+)-(5S,6R)-6-[(benzyloxy)methyl]-5-hydroxy-1-methoxy-5,6-dihydropyridin-2(1H)-one 
• 1304540-36-0 C₁₄H₁₇NO₄ 
• 1304540-32-6 (+)-N-{(1'S)-1-[(benzyloxy)methyl]prop-2-en-1-yl}-N-methoxybut-3-enamide 
• 1304540-34-8 (-)-(6S)-6-[(benzyloxy)methyl]-1-methoxy-3,6-dihydropyridin-2(1H)-one 

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

Enantioselective iridium-catalyzed allylic substitutions with hydroxamic acid derivatives as N-nucleophiles

Enantioselective Ir-catalyzed allylic aminations with hydroxamic acid derivatives are described. Catalysts were prepared in situ from [Ir(cod)Cl] 2 or [Ir(dbcot)Cl]2, a phosphoramidite and base. In addition, pure (φ-allyl)Ir complexe