1315340-95-4

Upstream product

• 1315340-94-3 4-(2-benzyloxy-phenyl)-4-(tert-butyldimethylsilanyloxy)-1-(1,4,5,6,8-pentamethoxy-naphthalen-2-yl)-butan-2-one 
• 1315340-93-2 4-(2-benzyloxy-phenyl)-4-hydroxy-1-(1,4,5,6,8-pentamethoxy-naphthalen-2-yl)-butan-2-one 
• 1315340-90-9 1,2,4,5,8-pentamethoxy-6-(2-nitro-ethyl)-naphthalene 
• 1315340-92-1 5-(2-benzyloxy-phenyl)-3-(1,4,5,6,8-pentamethoxynaphthalen-2-ylmethyl)-4,5-dihydro-isoxazole 
• 122182-21-2 1,2,4,5,8-pentamethoxynaphthalene 
• 114263-49-9 1,4,5,6,8-pentamethoxynaphthalene-2-carbaldehyde 

Downstream Products

• 1315340-99-8 C₂₃H₂₂O₇ 
• 1315340-97-6 6-[4-(tert-butyldimethylsilanyloxy)-4-(2-hydroxy-phenyl)-2-oxo-butyl]-2,5,8-trimethoxy-[1,4]naphthoquinone 
• 1315340-98-7 6-[4-(tert-butyldimethylsilanyloxy)-4-(2-hydroxy-phenyl)-2-oxo-butyryl]-2,5,8-trimethoxy-[1,4]naphthoquinone 

Relevant academic research and scientific papers

Alternative spiroketalization methods toward purpuromycin: A hemiketal conjugate addition strategy and use of an electron-rich isocoumarin precursor

Two methods are presented that were designed to circumvent the persistent problem of benzofuran formation and instead yield a spiroketal of the rubromycin family type. First, using an alternative disconnection, a hemiketal conjugate addition to a naphthaq