948837-52-3

Upstream product

• 948837-58-9 C₉H₁₅O₂I 
• 948837-51-2 C₂₁H₃₁O₃SiBr 
• 1461-22-9 tributyltin chloride 
• 627461-50-1 (+)-(2S)-4-pentyne-1,2-diol 
• 948837-50-1 C₂₆H₄₀O₅Si 
• 948837-49-8 C₂₀H₃₂O₄Si 
• 948837-60-3 C₁₉H₃₁O₃BrSi 
• 948837-48-7 C₁₄H₂₃O₂BrSi 
• 948837-59-0 C₁₅H₂₃O₃BrSi 
• 948837-47-6 (S,E)-5-iodo-4-methylpent-4-ene-1,2-diol 
• 55289-15-1 methyl 6-bromo-3-hydroxy-2-methylbenzoate 
• 55289-05-9 methyl 3-hydroxy-2-methylbenzoate 
• 1975-50-4 2-methyl-3-nitrobenzic acid 
• 59382-59-1 2-methyl-3-nitro-benzoic acid methyl ester 

Downstream Products

• 948837-61-4 C₂₇H₄₂O₅Si 
• 948837-53-4 C₃₁H₅₄O₄Si₂ 
• 948837-54-5 C₃₁H₅₂O₅Si₂ 

Relevant academic research and scientific papers

A transannular diels-alder strategy to the construction of the CDE ring system of nakiterpiosin

The transannular Diels-Alder (TADA) reaction was applied to the synthesis of the CDE ring system of nakiterpiosin (1). TADA product 28 is a key intermediate toward the total synthesis of 1.

Studies toward the total synthesis of nakiterpiosin: construction of the CDE ring system by a transannular Diels-Alder strategy

The transannular Diels-Alder (TADA) reaction was applied to the synthesis of the CDE ring system of nakiterpiosin (1). Tetracyclic compound 25 may be a key intermediate in the total synthesis of 1.