287728-33-0

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 287728-32-9 (S)-4-phthalimido-1-(tert-butyldimethylsilyloxy)butan-2-ol 
• 136918-14-4 phthalimide 
• 287728-23-8 (S)-4-phthalimido-2-(tert-butyldiphenylsilyl)oxy-1-(tert-butyldimethylsilyl)oxybutane 
• 287728-30-7 (S)-2,2-dimethyl-4-(2-phthalimidoethyl)-1,3-dioxolane 
• 287728-31-8 (S)-4-phthalimido-1,2-butanediol 

Downstream Products

• 287728-34-1 ethyl (2E,4S)-6-(1,3-dihydro-3-hydroxy-1-oxoisoindol-2-yl)-4-(tert-butyldiphenylsilyl)oxyhex-2-enoate 
• 287728-24-9 ethyl (2E,4S)-4-(tert-butyldiphenylsilyl)oxy-6-phthalimidohex-2-enoate 
• 287728-28-3 (1R,2S,10bR)-1,2,3,10b-tetrahydro-1-ethoxycarbonylmethyl-2-(tert-butyldiphenylsilyl)oxypyrido[2,1-a]isoindol-6(4H)-one 
• 287728-22-7 ethyl (2E,4S)-6-(1,3-dihydro-3-phenylsulfanyl-1-oxoisoindol-2-yl)-4-(tert-butyldiphenylsilyl)oxyhex-2-enoate 
• 287728-26-1 (1S,2S,10bS)-1,2,3,10b-tetrahydro-1-ethoxycarbonylmethyl-10b-phenylsulfanyl-2-(tert-butyldiphenylsilyl)oxypyrido[2,1-a]isoindol-6(4H)-one 
• 618388-51-5 4-(1-allyl-3-oxo-1-phenylsulfanyl-1,3-dihydro-isoindol-2-yl)-2-(tert-butyl-diphenyl-silanyloxy)-butyraldehyde 
• 618388-44-6 (2S)-4-(1,3-dihydro-3-hydroxy-1-oxoisoindol-2-yl)-2-(tert-butyldiphenylsilyl)oxy-1-(tert-butyldimethylsilyl)oxybutane 
• 618388-45-7 (2S)-4-(3-allyl-2,3-dihydro-3-phenylsulfanyl-1-oxoisoindol-2-yl)-2-(tert-butyldiphenylsilyl)oxy-1-butanol 
• 618388-49-1 2-[4-(tert-butyl-dimethyl-silanyloxy)-3-(tert-butyl-diphenyl-silanyloxy)-butyl]-3-phenylsulfanyl-2,3-dihydro-isoindol-1-one 
• 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 
• 618388-48-0 [2-(tert-butyl-diphenyl-silanyloxy)-6-oxo-1,2,3,4,6,10b-hexahydro-pyrido[2,1-a]isoindol-1-yl]-acetic acid ethyl ester 
• 287728-23-8 (S)-4-phthalimido-2-(tert-butyldiphenylsilyl)oxy-1-(tert-butyldimethylsilyl)oxybutane 
• 618388-42-4 (S)-4-phthalimido-2-(tert-butyldiphenylsilyl)oxy-1-butanal 

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

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

Stereoselective cyclisation of malic acid-derived α-sulfanyllactam (1) via radical and carbanionic intermediates affords stereo-defined tetrahydropyrido[2,1-a]isoindolones as model compounds for the D/E cis-ring fusion of the Tacaman indole alkaloid skele