478314-20-4

Upstream product

• 2244-16-8 (S)-p-mentha-6,8-dien-2-one 
• 478314-44-2 (S)-5-Isopropenyl-2-methyl-6-(3-methyl-but-2-enyl)-cyclohex-2-enone 
• 870-63-3 prenyl bromide 
• 478314-18-0 (5R,6S)-6-Hydroxymethyl-5-isopropenyl-2-methyl-6-(3-methyl-but-2-enyl)-cyclohex-2-enone 

Downstream Products

• 478314-24-8 (S)-2-[(1R,2S,3S,4R)-2-(tert-Butyl-dimethyl-silanyloxymethyl)-3-methoxymethoxy-4-methyl-2-(3-methyl-but-2-enyl)-cyclohexyl]-propan-1-ol 
• 478314-22-6 tert-Butyl-[(1S,2S,3R,6R)-6-isopropenyl-2-methoxymethoxy-3-methyl-1-(3-methyl-but-2-enyl)-cyclohexylmethoxy]-dimethyl-silane 
• 478314-26-0 2,2-Dimethyl-propionic acid (S)-2-[(1R,2S,3S,4R)-2-hydroxymethyl-3-methoxymethoxy-4-methyl-2-(3-methyl-but-2-enyl)-cyclohexyl]-propyl ester 

Relevant academic research and scientific papers

Total synthesis and absolute configuration of marine bisnor-diterpenoid elisabethin C

Total synthesis of marine bisnor-diterpenoid elisabethin C was successfully carried out by stereoselective construction of bicyclo[4.3.0]nonane ring system with Dieckmann cyclization as the key step. The absolute configuration of elisabethin C was determined based on this total synthesis.