1598413-59-2

Upstream product

• 1598413-58-1 C₃₇H₅₀O₆Si 
• 186641-79-2 (R)-4-((tert-Butyldiphenylsilyl)oxy)-3-methylbutanal 
• 144693-95-8 (4R)-5-(tert-butyldiphenylsilyloxy)-4-methyl-1-pentene 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 1598413-57-0 (2R,4S,6S)-2-((R)-3-(tert-butyldiphenylsilyloxy)-2-methylpropyl)-6-(2-(4-methoxybenzyloxy)ethyl)tetrahydro-2H-pyran-4-ol 
• 1598413-56-9 (4S,6R)-7-(tert-butyldiphenylsilyloxy)-6-methylhept-1-en-4-yl 3-(4-methoxybenzyloxy) propanoate 
• 1598413-55-8 (4S,6R)-7-(tert-butyldiphenylsilyloxy)-6-methylhept-1-en-4-ol 

Downstream Products

• 1598413-60-5 (R)-3-((2R,4S,6S)-4-(tert-butyldimethylsilyloxy)-6-(2-(4-methoxybenzyloxy)ethyl)tetrahydro-2H-pyran-2-yl)-2-methylpropan-1-ol 
• 1598413-61-6 tert-butyl-((2S,4S,6R)-2-(2-(4-methoxybenzyloxy)ethyl)-6-((R)-2-methylbut-3-enyl)tetrahydro-2H-pyran-4-yloxy)dimethylsilane 
• 1598413-62-7 C₂₅H₄₂O₅Si 

Relevant academic research and scientific papers

Formal total synthesis of mandelalide A

Abstract: In this article the formal total synthesis of mandelalide A has been described in details. The highly convergent and flexible strategy developed for mandelalide A involved the construction of key building blocks ent-9 and 7, and their assembly t

Synthesis of proposed aglycone of mandelalide A

A highly convergent synthesis of the proposed mandelalide A aglycone is reported. The cornerstones of the synthetic strategy include the following: E-selective intramolecular Heck cyclization, Masamune-Roush olefination, Stork-Zhao-Wittig olefination, mod