908338-99-8

Upstream product

• 908338-93-2 triethyl-[1,4,5,7,8-pentamethoxy-3-(2-nitro-ethyl)-naphthalen-2-yloxy]-silane 
• 67191-36-0 1-(benzyloxy)-2-ethenylbenzene 
• 105518-05-6 3,4,6-trimethoxy-phthalic acid dimethyl ester 
• 908338-91-0 2,3-bis-(tert-butyl-dimethyl-silanyloxymethyl)-1,4,5,6,8-pentamethoxy-naphthalene 
• 908339-10-6 3-(tert-butyl-dimethyl-silanyloxymethyl)-1,4,5,6,8-pentamethoxy-naphthalene-2-carbaldehyde 
• 908339-12-8 [1,4,5,7,8-pentamethoxy-3-(2-nitro-ethyl)-naphthalen-2-yl]-methanol 
• 154955-86-9 1,4-dihydroxy-5,6,8-trimethoxy-naphthalene-2,3-dicarboxylic acid dimethyl ester 
• 908339-08-2 1,4,5,6,8-pentamethoxy-naphthalene-2,3-dicarboxylic acid dimethyl ester 
• 908339-13-9 1,4,5,7,8-pentamethoxy-3-(2-nitro-ethyl)-naphthalene-2-carbaldehyde 
• 908339-09-3 (3-hydroxymethyl-1,4,5,7,8-pentamethoxy-naphthalen-2-yl)-methanol 
• 908338-92-1 tert-butyl-dimethyl-[1,4,5,7,8-pentamethoxy-3-(2-nitro-ethyl)-naphthalen-2-ylmethoxy]-silane 

Downstream Products

• 908339-17-3 4-(2-benzyloxy-phenyl)-4-hydroxy-1-(3-hydroxy-1,4,5,6,8-pentamethoxy-naphthalen-2-yl)-butan-2-one 
• 908339-25-3 3-[5-(2-benzyloxy-phenyl)-4,5-dihydro-isoxazol-3-ylmethyl]-1,4,5,7,8-pentamethoxy-naphthalen-2-ol 

Relevant academic research and scientific papers

Investigation of a convergent route to purpuromycin: Benzofuran formation vs spiroketalization

A mild and efficient [3+2] nitrile oxide/olefin cycloaddition allows coupling of the highly functionalized naphthalene and isocoumarin hemispheres of purpuromycin. A rationale of the inability of advanced keto alcohols to spirocyclize is presented based u