1280608-57-2

Upstream product

• 67-56-1 methanol 
• 1280608-53-8 C₂₈H₂₉NO₇ 
• 1280608-49-2 C₂₁H₂₁NO₆ 
• 1280608-40-3 C₂₃H₂₅NO₆ 
• 1280608-50-5 C₂₃H₂₇NO₆ 
• 1280608-51-6 C₃₀H₃₃NO₆ 
• 1280608-52-7 C₃₀H₃₃NO₇ 

Downstream Products

• 1280608-59-4 C₃₀H₃₃NO₉ 
• 1280608-61-8 C₃₃H₄₃NO₉Si 
• 1280608-62-9 C₃₃H₄₁NO₉Si 
• 1280608-67-4 C₃₉H₅₀N₂O₁₁Si 
• 1280608-87-8 C₃₄H₃₆N₂O₁₀ 
• 1280608-68-5 C₃₄H₃₄N₂O₁₀ 
• 1280608-60-7 C₃₆H₅₁NO₉Si₂ 

Relevant academic research and scientific papers

Total synthesis and absolute stereochemistry of seragakinone A

(Chemical Equation Presented) Cyclic transformation: The key transformations of the asymmetric total synthesis of the marine-derived natural product seragakinone A are two N-heterocyclic carbene catalyzed benzoin cyclizations that result in the construction of two rings and a pinacol-type rearrangement to install the angular prenyl substituent.