478930-77-7

Upstream product

• 58795-27-0 (4aS,8aS)-1,1,4a-Trimethyl-5,6-dimethylene-decahydro-naphthalene 
• 166900-19-2 C₁₅H₂₄O 
• 178394-53-1 Formic acid (1S,4aS,8aS)-5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-ylmethyl ester 
• 3243-36-5 (1S,4aS,8aS)-1,2,3,4,4a,5,6,7,8,8a-decahydro-5,5,8a-trimethyl-2-methylene-1-naphthaleneacetaldehyde 
• 31207-72-4 13,14,15,16-tetranorlabd-8⁽¹⁷⁾-en-12-ol 
• 54632-04-1 albicanol 
• 596-85-0 (+)-manool 
• 10266-75-8 4-((1S,4aS,8aS)-5,5,8a-trimethyl-2-methylene-decahydronaphthalen-1-yl)butan-2-one 
• 29065-24-5 2-((1S, 4aS, 8aS)-5,5,8a-trimethyl-2-methylenedecahydronaphthalen-1-yl)acetic acid 
• 2139-44-8 2-(4-(tetrahydro-2H-pyran-2-yloxy)phenoxy)tetrahydro-2H-pyran 
• 155551-30-7 (1S,4aS,8aS)-3H-2-methylene-1,4,4a,5,6,7,8,8a-octahydro-5,5,8a-trimethylnaphthalene-1-carboxaldehyde 

Downstream Products

• 39707-56-7 (+)-zonarone 
• 478930-78-8 (-)-ent-zonarol di-THP ether 

Relevant academic research and scientific papers

New access to sesquiterpene hydroquinones: Synthesis of (+)-ent-chromazonarol

A facile access to optically active (+)-ent-chromazonarol ent-1, isolated from the sponge Disidea pallescens, is reported from commercially available (+)-manool 4. Copyright Taylor & Francis LLC.

Highly efficient synthesis of the optically active sesquiterpene hydroquinone (+)-zonarol and the sesquiterpene quinone (+)-zonarone

A facile synthesis of the sesquiterpene hydroquinone (+)-zonarol 5 and sesquiterpene quinone (+)-zonarone 6 from manool is reported in 7 and 8 steps, respectively.