7706-85-6

Upstream product

• 186581-53-3 diazomethane 
• 73389-34-1 4-(3-hydroxy-phenyl)-5H-furan-2-one 
• 766-85-8 3-methoxy-1-iodobenzene 
• 857618-76-9 2-acetoxy-1-(3-acetoxy-phenyl)-ethanone 
• 3095-95-2 diethylphosphonoacetic acid 
• 5000-65-7 2-bromo-3'-methoxyacetophenone 

Downstream Products

• 1373247-33-6 (3S,4R)-benzyl 3-(3-methoxy-3-oxopropyl)-4-(3-methoxyphenyl)-2-oxotetrahydrofuran-3-carboxylate 
• 1373247-35-8 (5S,9R)-9-(3-methoxyphenyl)-7-oxa-1-azaspiro[4.4]nonane-2,6-dione 
• 1373247-37-0 (5S,9R)-9-(2,4-dibromo-5-methoxyphenyl)-7-oxa-1-azaspiro[4.4]nonane-2,6-dione 
• 1373247-25-6 (5S,9R)-9-(2,4-dibromo-5-methoxyphenyl)-7-methyl-1,7-diazaspiro[4.4]nonane-2,6,8-trione 
• 1373247-39-2 C₁₅H₁₆Br₂N₂O₄ 

Relevant academic research and scientific papers

Total syntheses of all the amathaspiramides

Six in one blow: Total syntheses of all the amathaspiramide alkaloids have been accomplished. Rapid construction of the diazaspiro[3.3]nonane core combined with regio- and diastereoselective reduction of the cyclic imide moiety with DIBAL established the route to the common structural motif. The late-stage reduction of the lactam to an imine functionality mediated by Schwartz's reagent was the key to the streamlined syntheses. Copyright

An expedient palladium-mediated route to 3-arylfurans

A facile route to 3-arylfurans has been developed by employing the Heck reaction between 2,5-dihydro-2,5-dimethoxyfuran and aryl iodides as the key step.