613661-48-6

Upstream product

• 613661-39-5 Methanesulfonic acid (1R,4aS,5R,8aS)-4a,5,8a-trimethyl-2-oxo-decahydro-naphthalen-1-ylmethyl ester 
• 613661-38-4 (1R,4aS,5R,8aS)-1-hydroxymethyl-4a,5,8a-trimethyl-3,4,4a,5,6,7,8,8a-octahydro-1H-naphthalen-2-one 
• 613661-42-0 (4aS,5R,8aR)-4a,5,8a-trimethyl-1-methylene-3,4,4a,5,6,7,8,8a-octahydro-1H-naphthalen-2-one 
• 108-98-5 thiophenol 
• 252290-05-4 (-)-(4aS,5R)-4,4a,5,6,7,8-hexahydro-4a,5-dimethyl-2(3H)-naphthalenone 
• 252290-09-8 (4aS,5R)-3,4,4a,5,6,7-hexahydro-4a,5-dimethyl-2H-1-benzopyran-2-one 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 613661-47-5 (1S,4aS,5R,8aS)-1-phenylsulfanylmethyl-4a,5,8a-trimethyl-3,4,4a,5,6,7,8,8a-octahydro-1H-naphthalen-2-one 

Relevant academic research and scientific papers

Synthesis of (-)-nakamurol A and assignment of absolute configuration of diterpenoid (+)-nakamurol A

The total synthesis of the enantiomer of the marine sponge diterpenoid nakamurol A and determination of the absolute configuration of this natural product are reported. This first synthetic entry to thelepogane-type diterpenoids involves the use of the bi