1286210-52-3

Upstream product

• 1286210-10-3 C₂₅H₂₈O₃Si 
• 1286210-44-3 C₁₄H₁₆O₄ 
• 1286210-13-6 C₁₅H₁₉NO₃ 
• 1286210-46-5 C₁₄H₁₇NO₃ 
• 1286210-23-8 C₁₅H₁₉NO₄ 
• 1286210-25-0 C₁₅H₁₈ClNO₄ 
• 1286210-26-1 C₃₉H₄₂ClNO₆Si 
• 1286210-34-1 C₃₉H₄₂ClNO₆Si 
• 75-36-5 acetyl chloride 
• 1286210-20-5 C₂₄H₂₅BrO₃Si 
• 1286210-43-2 C₂₃H₂₅BrO₃Si 
• 16414-34-9 3-bromo-4,5-dihydroxybenzaldehyde 
• 2973-76-4 5-bromo-4-hydroxy-3-methoxybenzaldehyde 
• 23354-30-5 3-bromo-4-methoxy-5-hydroxybenzaldehyde 

Relevant academic research and scientific papers

Synthesis and biological evaluation of ABCD ring fragments of the kibdelones

Arylation goes platinum: The synthesis of the ABCD ring fragments of the kibdelones has been achieved through a novel PtIV-catalyzed arylation of a quinone monoketal followed by photocyclization (see scheme). Biological evaluation in the NCI 60-cell screen revealed that the kibdelone ABCD ring analogues were about 2000 times less active than kibdelones B and C, suggesting that the tetrahydroxanthone structure of the kibdelones is crucial for cytotoxicity. Copyright