123995-08-4

Upstream product

• 123995-09-5 (4α,4aα,8aβ)-octahydro-7,7-dimethoxy-4-(methoxymethoxy)-4a-methyl-1(2H)-naphthalenone 
• 123995-12-0 (2α,4aα,5α,8α,8aβ)-1-(decahydro-8-hydroxy-5-(methoxymethoxy)-4a,8-dimethyl-2-naphthalenyl)ethanone 
• 123995-13-1 (1α,4α,4aα,7α,8aβ)-decahydro-4-(methoxymethoxy)-1,4a-dimethyl-7-(1-methylethenyl)-1-naphthalenol 
• 123995-11-9 (1α,4α,4aα,8aβ)-decahydro-7-ethylidene-4-(methoxymethoxy)-1,4a-dimethyl-1-naphthalenol 
• 123995-10-8 (4α,4aα,8α,8aβ)-octahydro-8-hydroxy-5-(methoxymethoxy)-4a,8-dimethyl-1(2H)-naphthalenone 
• 87262-05-3 4β-Hydroxy-4aβ-methyl-3,4,4a,5,6,8aα-hexahydronaphthalene-1(2H),7(8H)-dione 7-dimethyl acetal 
• 123995-14-2 (1α,4α,4aα,7α,8aβ)-decahydro-4-(methoxymethoxy)-1,4a-dimethyl-7-(1-methylethyl)-1-naphthalenol 
• 124095-91-6 (1α,4α,4aα,7α,8aβ)-decahydro-1,4a-dimethyl-7-(1-methylethyl)-1,4-naphthalenediol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 124095-90-5 (+/-)-5-epi-nardol 

Relevant academic research and scientific papers

Base-Induced and -Directed Rearrangements of 4-Monotosylated Perhydronaphthalene-1,4-diols. Synthesis of (+/-)-5-epi-Nardol

The utility of perhydronaphthalene precursors for the synthesis of sesquiterpenes which possess a cis-fused perhydroazulene skeleton with an exocyclic methylene unit has been examined.For this purpose the tosylates 3, 4, 28, and 29 were prepared, and thei