526217-86-7

Upstream product

• 24470-78-8 isopropyltriphenylphosphonium iodide 
• 526217-85-6 (5E,7Z)-(2R,4S)-2-[2,5-Bis-(tert-butyl-dimethyl-silanyloxy)-4-methoxy-3-methyl-phenyl]-4-methyl-nona-5,7-dienal 
• 526217-87-8 4-benzyl-3-{[2,5-bis-(tert-butyl-dimethyl-silanyloxy)-4-methoxy-3-methyl-phenyl]-acetyl}-oxazolidin-2-one 
• 526217-78-7 [2,5-bis-(tert-butyl-dimethyl-silanyloxy)-4-methoxy-3-methyl-phenyl]-acetic acid ethyl ester 
• 526217-79-8 [2,5-bis-(tert-butyl-dimethyl-silanyloxy)-4-methoxy-3-methyl-phenyl]-acetic acid 
• 526217-76-5 1-bromo-2,5-bis-(tert-butyl-dimethyl-silanyloxy)-4-methoxy-3-methyl-benzene 
• 526217-80-1 (E)-(R)-4-Methyl-5-trityloxy-pent-2-enoic acid methoxy-methyl-amide 
• 526217-82-3 C₂₇H₂₈O 
• 526217-81-2 (E)-(R)-4-Methyl-5-trityloxy-pent-2-enal 
• 526217-83-4 (2Z,4E)-(R)-7-Iodo-6-methyl-hepta-2,4-diene 
• 526217-89-0 (3E,5Z)-(R)-2-Methyl-hepta-3,5-dien-1-ol 
• 7149-92-0 2,4-dimethoxy-3-methylbenzaldehyde 
• 19676-67-6 2,4-dimethoxy-3-methylphenol 
• 2207-57-0 2-methoxy-3-methyl-1,4-benzoquinone 

Relevant academic research and scientific papers

Total synthesis of elisabethin A: Intramolecular Diels-Alder reaction under biomimetic conditions

We describe the first total synthesis of the marine diterpenoid elisabethin A. The synthesis uses (S)-hydroxy-2-methyl-propionate as the chiral starting material, which is elaborated into a dienyl-iodide and added to an aryl acetic acid ester via enolate