1414124-64-3

Upstream product

• 1414124-48-3 (E)-1-[(3,7-dimethylocta-2,6-dienyl)oxy]-3,5-bis(methoxymethoxy)benzene 
• 6138-90-5 trans-geranyl bromide 

Downstream Products

• 1414124-94-9 (E)-5-{[3,4-bis(methoxymethoxy)phenyl]ethynyl}-2-(3,7-dimethylocta-2,6-dienyl)-1,3-bis(methoxymethoxy)benzene 
• 1414125-07-7 5-[(Z)-3,4-bis(methoxymethoxy)styryl]-2-[(E)-3,7-dimethylocta-2,6-dienyl]-1,3-bis(methoxymethoxy)benzene 
• 848190-46-5 5-[(E)-3,4-bis(methoxymethoxy)styryl]-2-[(E)-3,7-dimethylocta-2,6-dienyl]-1,3-bis(methoxymethoxy)benzene 
• 1414124-79-0 (E)-4-(3,7-dimethylocta-2,6-dienyl)-3,5-bis(methoxymethoxy)phenyl trifluoromethanesulfonate 

Relevant academic research and scientific papers

Palladium-catalyzed routes to geranylated or farnesylated phenolic stilbenes: Synthesis of pawhuskin C and schweinfurthin J

Starting from double MOM-protected phloroglucinol, the facile total syntheses of bioactive natural products pawhuskin C and schweinfurthin J were accomplished in good overall yields. The Heck, Stille, or Suzuki coupling reactions of two different electron