680221-24-3

Upstream product

• 680220-77-3 5-methoxycarbonyloxy-2,2-dimethyl-3-pentyn-1-ol 
• 680220-87-5 5-(4-methoxyphenoxycarbonyloxy)-2,2-dimethyl-3-pentyn-1-ol 
• 150-76-5 4-methoxy-phenol 
• 92156-87-1 2,2-dimethyl-3-(4-methoxyphenylmethoxy)propionaldehyde 
• 853296-71-6 1-(4-methoxyphenoxycarbonyloxy)-5-(4-methoxybenzyloxy)-4,4-dimethyl-2-pentyne 
• 853296-72-7 1-methoxycarbonyloxy-5-(4-methoxybenzyloxy)-4,4-dimethyl-2-pentyne 
• 853296-64-7 1-(4,4-dibromo-2,2-dimethyl-but-3-enyloxymethyl)-4-methoxy-benzene 
• 853296-65-8 5-(4-methoxybenzyloxy)-4,4-dimethyl-2-pentyn-1-ol 

Relevant academic research and scientific papers

Palladium-catalyzed cyclization reactions of propargylic carbonates with nucleophiles: A methodology for the syntheses of substituted 2,3-dihydrofurans and benzofurans

Phenoxy-substituted 2,3-dihydrofurans were synthesized by the palladium-catalyzed reaction of 5-methoxycarbonyloxy-3-pentyn-1-ol with phenols. The propargylic carbonate containing a nucleophilic phenoxy group also reacted in the presence of palladium to p

Facile syntheses of substituted 2,3-dihydrofurans and benzofurans by palladium-catalyzed reactions of propargylic carbonates with nucleophiles

Substituted 2,3-dihydrofurans and benzofurans are synthesized by the palladium-catalyzed reaction of 5-methoxycarbonyloxy-3-pentyn-1-ols and 1-(2-hydroxyphenyl)-3-methoxycarbonyloxy-1-propyne with nucleophiles, respectively. Various substituted propargyli