618388-49-1

Upstream product

• 108-98-5 thiophenol 
• 618388-44-6 (2S)-4-(1,3-dihydro-3-hydroxy-1-oxoisoindol-2-yl)-2-(tert-butyldiphenylsilyl)oxy-1-(tert-butyldimethylsilyl)oxybutane 
• 287728-30-7 (S)-2,2-dimethyl-4-(2-phthalimidoethyl)-1,3-dioxolane 
• 287728-32-9 (S)-4-phthalimido-1-(tert-butyldimethylsilyloxy)butan-2-ol 
• 287728-33-0 (S)-4-phthalimido-2-(tert-butyldiphenylsilyl)oxy-1-butanol 
• 287728-23-8 (S)-4-phthalimido-2-(tert-butyldiphenylsilyl)oxy-1-(tert-butyldimethylsilyl)oxybutane 
• 287728-31-8 (S)-4-phthalimido-1,2-butanediol 
• 136918-14-4 phthalimide 

Downstream Products

• 618388-50-4 3-allyl-2-[4-(tert-butyl-dimethyl-silanyloxy)-3-(tert-butyl-diphenyl-silanyloxy)-butyl]-3-phenylsulfanyl-2,3-dihydro-isoindol-1-one 
• 618388-51-5 4-(1-allyl-3-oxo-1-phenylsulfanyl-1,3-dihydro-isoindol-2-yl)-2-(tert-butyl-diphenyl-silanyloxy)-butyraldehyde 
• 618388-45-7 (2S)-4-(3-allyl-2,3-dihydro-3-phenylsulfanyl-1-oxoisoindol-2-yl)-2-(tert-butyldiphenylsilyl)oxy-1-butanol 

Relevant academic research and scientific papers

Stereoselective tetrapyrido[2,1-a]isoindolone synthesis via carbanionic and radical intermediates: a model study for the Tacaman alkaloid D/E ring fusion.

Cyclization under both radical and carbanionic conditions of N-substituted 3-phenylsulfanylisoindolin-1-one 14 containing a chiral N-tether incorporating an enoate ester as the acceptor leads to tetrahydropyrido[2,1-a]isoindolones stereoselectively. The m