1370641-48-7

Upstream product

• 52750-05-7 ethyl (E)-3-(4-methoxyphenyl)-2-methylpropenoate 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 122-84-9 4-methoxybenzyl methyl ketone 
• 1228457-91-7 ethyl (1S,5S)-1-ethyl-3-hydroxy-5-(4-methoxyphenyl)-4-methyl-2-oxocyclopent-3-enecarboxylate 
• 1228457-77-9 ethyl (E)-2-ethyl-6-(4-methoxyphenyl)-5-methyl-3,4-dioxohex-5-enoate 
• 1370641-30-7 (S)-3-((1E,4Z)-1-(4-methoxyphenyl)-2-methyl-3-oxodeca-1,4-dien-4-yl)-4-phenyloxazolidin-2-one 
• 1370641-23-8 (R)-3-(4-methoxyphenyl)-2-methyl-4-pentylcyclopent-2-enone 
• 1370641-22-7 (S)-3-((1R,3S,4R,5S)-4-(4-methoxyphenyl)-3-methyl-3-(1-methyl-1H-indol-3-yl)-2-oxo-5-pentylcyclopentyl)4-phenyloxazolidin-2-one 
• 1370641-09-0 (S)-3-((1R,2S)-3-(4-methoxyphenyl)-4-methyl-5-oxo-2-pentylcyclopent-3-enyl)-4-phenyloxazolidin-2-one 
• 1361029-67-5 (Z)-methyl 3-(4-methoxyphenyl)-2-methyl-3-(3-methyl-1H-indol-2-yl)acrylate 
• 1361029-56-2 1-(4-methoxyphenyl)-2,9-dimethyl-3H-pyrrolo[1,2-a]indol-3-one 

Relevant academic research and scientific papers

Macrolide Synthesis through Intramolecular Oxidative Cross-Coupling of Alkenes

A RhIII-catalyzed intramolecular oxidative cross-coupling between double bonds for the synthesis of macrolides is described. Under the optimized reaction conditions, macrocycles containing a diene moiety can be formed in reasonable yields and with excellent chemo- and stereoselectivity. This method provides an efficient approach to synthesize macrocyclic compounds containing a 1,3-conjugated diene structure.