397872-80-9

Upstream product

• 849769-11-5 1-(benzo[d][1,3]dioxol-6-yl)-3-(trimethylsilyl)prop-2-yn-1-ol 
• 95-01-2 2,4-Dihydroxybenzaldehyde 
• 120-57-0 piperonal 
• 2620-47-5 1-(benzo[d][1,3]dioxol-5-yl)prop-2-yn-1-ol 
• 397872-79-6 methanesulfonic acid 4-formyl-3-methanesulfonyloxyphenyl ester 

Downstream Products

• 397872-58-1 acetic acid 4-acetoxy-1-benzo[1,3]dioxol-5-yl-4-(2,4-bis-metanesulfonylphenyl)-but-2-ynyl ester 
• 397872-59-2 acetic acid 3-(acetoxybenzo[1,3]dioxol-5-ylmethyl)-1-(2,4-bismethanesulfonyloxyphenyl)-2-methylenebut-3-enyl ester 
• 397872-60-5 methanesulfonic acid 4-(3-benzo[1,3]dioxol-5-ylmethyl-2-methylenebut-3-enyl)-3-methanesulfonyloxyphenyl ester 
• 158081-97-1 anolignan A 

Relevant academic research and scientific papers

Syntheses of anolignans A and B using ruthenium-catalyzed cross-enyne metathesis

Anolignans A and B were synthesized using ruthenium-catalyzed cross-enyne metathesis as the key steps. The 1,3-diene moieties of these natural products were constructed by the introduction of the methylene parts of ethylene into alkyne using Grubbs' catalyst.