162292-19-5

Upstream product

• 162292-64-0 2-(4-Methoxy-phenyl)-3-methyl-but-2-en-1-ol 
• 162292-66-2 2-(4-Methoxyphenyl)-3-methyl-2-butenal 
• 33131-26-9 2-(4-Methoxy-phenyl)-3-methyl-but-2-enoic acid methyl ester 
• 162292-73-1 3-(4-Methoxy-phenyl)-2-methyl-hept-2-en-5-yn-4-ol 

Relevant academic research and scientific papers

Enynones in organic synthesis. 7. Substituent effects on the α-tocopherol-catalyzed cyclization of enynones to methylenecyclopentenones. Convenient syntheses of members of the methylenomycin class of antibiotics

Substituent effects on the α-tocopherol (vitamin E, 3b) catalyzed cyclization of a wide variety of enynones 1a-z to methylenecyclopentenones 7a-z have been examined, with particular emphasis given to electron-withdrawing and -donating groups at positions