88995-99-7

Upstream product

• 42856-43-9 1-benzylpiperidine-2,6-dione 
• 64-17-5 ethanol 

Downstream Products

• 88996-07-0 1-benzyl-6-ethoxy-3-<5-(trimethylsilyl)-3-pentynyl>-2-piperidinone 
• 88996-17-2 7-Benzyl-5-vinylidene-7-aza-bicyclo[4.2.2]decan-8-one 
• 88996-15-0 6-Benzyl-4-vinylidene-6-aza-bicyclo[3.2.2]nonan-7-one 
• 121823-63-0 1-benzyl-6-ethoxy-3-<6-(trimethylsilyl)-4-hexenyl>-2-piperidinone 
• 121823-72-1 1-Benzyl-3-hex-5-enyl-3,4-dihydro-1H-pyridin-2-one 
• 121823-71-0 7-Benzyl-5-vinyl-7-aza-bicyclo[4.2.2]decan-8-one 
• 88996-16-1 6-benzyl-4-endo-vinyl-6-azabicyclo<3.2.2>nonan-7-one 
• 88996-16-1 6-benzyl-4-exo-vinyl-6-azabicyclo<3.2.2>nonan-7-one 
• 88996-08-1 1-benzyl-6-ethoxy-3-<5-(trimethylsilyl)-3-pentenyl>-2-piperidinone 
• 88996-17-2 7-benzyl-5-vinylidene-7-azabicyclo<4.2.2>decan-8-one 
• 88996-09-2 1-benzyl-6-ethoxy-3-<6-(trimethylsilyl)-4-hexynyl>-2-piperidinone 
• 121823-53-8 1-benzyl-6-ethoxy-3-<4-(trimethylsilyl)-2-butynyl>-2-piperidinone 

Relevant academic research and scientific papers

ω-Alkoxy Lactams as Dipolar Synthons. Silicon-Assisted Synthesis of Azabicycles and a γ-Amino Acid

Alkylation of the lithium enolates derived from ω-alkoxy lactams 1a-c with unsaturated iodides 4 affords 5 in high yields (Table I).Those alkylation products 5, which contain an allyl- or propargylsilane moiety, undergo cyclization on acid treatment to fu

A novel synthetic route to 6-azabicyclooct-3-enes via silicon directed N-acyliminium chemistry. Synthesis of (+/-)-gabaculine

Alkylation of the lithium enolate, derived from 5-ethoxy-2-pyrrolidone 1 (Scheme 1), using alkyl halides containing either the vinylsilane or 2-propynylsilane moiety, provides substrates 3 for cyclization studies passing through N-acyliminium intermediate