1419186-72-3

Upstream product

• 850026-81-2 (S)-2-[(4S,5R,6S)-6-[(S)-2-(4-methoxybenzyloxy)-1-methylethyl]-2,2,5-trimethyl-1,3-dioxan-4-yl]propanal 
• 101979-45-7 (S)-3-acetyl-4-isopropyl-1,3-thiazolidine-2-thione 
• 850026-77-6 (R)-2-[(4S,5S,6S)-6-[(S)-2-(4-methoxybenzyloxy)-1-methylethyl]-2,2,5-trimethyl-1,3-dioxan-4-yl]-1-propanol 

Downstream Products

• 1419186-73-4 C₂₅H₄₁NO₇ 
• 140925-55-9 (3R,4S,5S,6S)-7-Benzyloxy-2,4,6-trimethyl-hept-1-ene-3,5-diol 
• 140925-78-6 C₂₀H₃₀O₃ 
• 1419186-75-6 C₂₀H₃₂O₄ 
• 1419186-84-7 C₂₀H₃₂O₄ 
• 1419186-85-8 C₂₀H₃₀O₄ 
• 1419186-71-2 C₂₁H₃₂O₃ 
• 116661-41-7 (2S,4R,5R)-1-(benzyloxy)-5-hydroxy-2,4,6-trimethylhept-6-en-3-one 
• 1419186-74-5 C₂₆H₄₃NO₇ 

Relevant academic research and scientific papers

Formal total synthesis of spirangien A

A formal total synthesis of the spiroketal containing cytotoxic myxobacteria metabolite spirangien A (1) is described. The approach utilizes a late introduction of the C20 alcohol that mirrors the biosynthesis of this compound. The key steps involved a hi