80765-07-7

Upstream product

• 24138-10-1 (+/-)-(4aβ,5β)-4,4a,5,6,7,8-hexahydro-5-hydroxy-1,4a-dimethylnaphthalen-2(3H)-one 
• 80765-03-3 trans-octahydro-1α-<(2,5-dimethoxyphenyl)methyl>-1β,4aβ-dimethyl-5β-hydroxy-2(1H)-naphthalenone 
• 80765-04-4 trans-decahydro-5α-<(2,5-dimethoxyphenyl)methyl>-5β,8aβ-dimethyl-6-methylene-1-naphthalenol 
• 60732-17-4 2,5-dimethoxybenzyl bromide 
• 80765-06-6 trans-decahydro-5α-<(2,5-dimethoxyphenyl)methyl>-5β,6β,8aβ-trimethyl-1-naphthalenol 

Downstream Products

• 61214-98-0 (4aS,5R,6S,8aS)-5-(2,5-Dimethoxy-benzyl)-1,5,6,8a-tetramethyl-decahydro-naphthalen-1-ol 
• 80795-33-1 (+/-)-avarol dimethyl ether 
• 80795-32-0 (+/-)-avarol 

Relevant academic research and scientific papers

Synthetic Studies of trans-Clerodane Diterpenoids and Congeners: Stereocontrolled Total Synthesis of (+/-)-Avarol

A stereocontrolled total synthesis of (+/-)-avarol, a sesquiterpenoid hydroquinone, has been accomplished in eight steps, by a flexible route which is potentially useful in the synthesis of related natural products containing a functionalized bicyclo4.4.