199180-36-4

Upstream product

• 199180-35-3 (1R,2S,4aR,8aS)-1-(2,5-Dimethoxy-benzyl)-1,2,4a-trimethyl-5-methylene-decahydro-naphthalene 
• 113666-06-1 (-)-(4aR)-1,4a-dimethyl-4,4a,7,8-tetrahydronaphthalene-2,5(3H,6H)-dione 
• 199180-20-6 5,8a-dimethyl-3,4,8,8a-tetrahydro-2H-spiro[naphthalene-1,2′-[1,3]dioxolan]-6(7H)-one 
• 199180-32-0 C₂₄H₃₆O₅ 
• 199180-34-2 (4aS,5R,6S,8aR)-5-(2,5-Dimethoxy-benzyl)-5,6,8a-trimethyl-octahydro-naphthalen-1-one 
• 199180-28-4 C₁₉H₃₂O₄ 
• 199180-31-9 C₁₇H₂₈O₂ 
• 199180-21-7 C₁₄H₂₂O₃ 
• 199180-33-1 C₂₆H₃₅F₃O₆ 
• 475301-82-7 C₂₅H₃₃F₃O₅ 
• 475301-81-6 C₂₃H₃₄O₄ 
• 475301-84-9 (1R,2S,4aR,8aS)-1-(2-Methoxy-benzyl)-1,2,4a-trimethyl-5-methylene-decahydro-naphthalene 
• 475301-83-8 (4aS,5R,6S,8aR)-5-(2-Methoxy-benzyl)-5,6,8a-trimethyl-octahydro-naphthalen-1-one 
• 199180-19-3 cis-decaline 

Downstream Products

• 87764-13-4 (+)-arenarol 

Relevant academic research and scientific papers

An efficient synthesis of (+)-aureol via boron trifluoride etherate-promoted rearrangement of (+)-arenarol

A novel marine natural product, (+)-aureol (1), was efficiently synthesized starting from the cis-fused decalin derivative 4. The synthetic method features boron trifluoride etherate-promoted rearrangement/cyclization reaction of (+)-arenarol (2) to form

Studies toward the synthesis of popolohuanone E: Synthesis of natural (+)-arenarol related to the proposed biogenetic precursor of popolohuanone E

The cis-fused decalin segment 6 required for the total synthesis of popolohuanone E (1) was efficiently synthesized starting from the enantiomerically pure (-)-Wieland-Miescher ketone derivative 9; the method features ortho ester Claisen rearrangement of