380600-52-2

Upstream product

• 380600-50-0 3-(4-isopropoxy-3-methoxy-phenyl)-cyclopent-2-enone 
• 22627-70-9 3-ethoxycyclopent-2-en-1-one 
• 108-24-7 acetic anhydride 
• 380600-51-1 3-(4-isopropoxy-3-methoxy-phenyl)-cyclopent-2-enol 
• 138505-27-8 4-bromo-1-isopropoxy-2-methoxy-benzene 

Downstream Products

• 380600-54-4 2-[1-(4-isopropoxy-3-methoxy-phenyl)-cyclopent-2-enyl]-acetamide 
• 380600-55-5 [1-(4-isopropoxy-3-methoxy-phenyl)-cyclopent-2-enyl]-acetonitrile 
• 380600-53-3 [1-(4-isopropoxy-3-methoxy-phenyl)-cyclopent-2-enyl]-acetic acid 

Relevant academic research and scientific papers

π-allyl cation cyclisations initiated by electrocyclic ring-opening of gem-dihalocyclopropanes: Application to the first total syntheses of the crinine-type alkaloids maritinamine and epi-maritinamine

The πallyl cation cyclisation initiated by electrocyclic ring-opening of gem-dihalocyclopropanes was presented. The application to the first total syntheses of the crinine-type alkaloids maritinamine and epi-maritinamine was discussed. The racemic modific