73483-87-1

Upstream product

• 115376-21-1 (4aS,5S,6S,8aS)-(-)-3,4,4a,5,6,7,8,8a-Octahydro-6-hydroxy-8a-methoxymethoxymethyl-5-methyl-5-(prop-2-enyl)naphthalen-1(2H)-one Ethylene Acetal 
• 115376-26-6 (1S,2S,4aS,8aS)-(-)-5,5-Ethylenedioxydecahydro-4a-methoxymethoxymethyl-1-methyl-1-(prop-2-enyl)naphthalen-2-yl S-Methyl Dithiocarbonate 
• 115376-29-9 (4aS,5S,8aS)-8a-Methoxymethoxymethyl-5-methyl-5-(4-methyl-pent-3-enyl)-1-oxo-decahydro-naphthalene-2-carboxylic acid methyl ester 
• 115376-30-2 (4aS,5S,8aS)-8a-Methoxymethoxymethyl-2,5-dimethyl-5-(4-methyl-pent-3-enyl)-octahydro-naphthalen-1-one 
• 115376-32-4 (4aS,5S,8aS)-8a-[1,3]Dioxolan-2-yl-2,5-dimethyl-5-(4-methyl-pent-3-enyl)-octahydro-naphthalen-1-one 
• 115376-31-3 (1S,4aS,8aS)-1,6-Dimethyl-1-(4-methyl-pent-3-enyl)-5-oxo-octahydro-naphthalene-4a-carbaldehyde 
• 115376-24-4 (4aS,5S,8aS)-8a-Hydroxymethyl-2,5-dimethyl-5-(4-methyl-pent-3-enyl)-octahydro-naphthalen-1-one 
• 115376-20-0 (4aS,5S,8aS)-(+)-3,4,4a,5,8,8a-Hexahydro-8a-methoxymethoxymethyl-5-methyl-5-(prop-2-enyl)naphthalene-1,6(2H,7H)-dione 1-Ethylene Acetal 
• 115392-88-6 (4aS,5S,8aS)-(-)-3,4,4a,5,6,7,8,8a-Octahydro-8a-methoxymethoxymethyl-5-methyl-5-(4-methylpent-3-enyl)naphthalen-1(2H)-one Ethylene Acetal 
• 98770-79-7 (S)-5,5-(ethylenedioxy)-2,3,4,4a,5,6,7,8-octahydro-4a-<(methoxymethoxy)methyl>-1-methylnaphthalene-2-one 
• 115376-28-8 (-)-3-<(1S,4aS,8aS)-5,5-Ethylenedioxydecahydro-4a-methoxymethoxymethyl-1-methylnaphthalen-1-yl>propanal 
• 115376-27-7 (4aS,5S,8aS)-(-)-3,4,4a,5,6,7,8,8a-Octahydro-8a-methoxymethoxymethyl-5-methyl-5-(prop-2-enyl)naphthalen-1(2H)-one Ethylene Acetal 
• 115376-23-3 (4aS,5S,8aS)-(-)-3,4,4a,5,6,7,8,8a-Octahydro-8a-methoxymethoxymethyl-5-methyl-5-(4-methylpent-3-enyl)naphthalen-1(2H)-one 
• 115376-22-2 (4aS,4S,8aS)-(-)-3,4,4a,5,6,7,8,8a-Octahydro-5-(3-hydroxypropyl)-8a-methoxymethoxymethyl-5-methyl-naphthalen-1(2H)-one Ethylene Acetal 

Relevant academic research and scientific papers

Total Synthesis of (+)-Perrottetianal A

The total synthesis of (+)-perrottetianal A, one of the sacculatane-type diterpenes isolated from liverworts, has been achieved starting from an optically active Wieland-Miescher ketone analogue.The ethylene glycol monoacetal of the starting material was

A Total Synthesis of (+)-Perrottetianal A

A total synthesis of (+)-perrottetianal A (1), one of the sacculatane diterpenes, has been achieved; the absolute stereochemistry of (1) is thus established as 4S,5S,10R.