24326-89-4

Upstream product

• 556-56-9 allyl iodid 
• 379736-69-3 (1R,4S)-2-(2-Benzyloxy-acetyl)-1,7,7-trimethyl-2-aza-bicyclo[2.2.1]heptan-3-one 
• 74-88-4 methyl iodide 
• 15082-42-5 lithium benzyloxide 

Downstream Products

• 250209-18-8 (1R,4S)-2-Benzyl-1,7,7-trimethyl-2-aza-bicyclo[2.2.1]heptan-3-one 
• 674303-46-9 (1S,4R)-3-{(3S)-3-azido-3-phenylpropyl}-3-aza-4,7,7-trimethylbicyclo[2.2.1]heptan-2-one 
• 911708-82-2 (1R,4S)-1,7,7-trimethyl-2-[2-(triphenylphosphanylidene)-acetyl]-2-aza-bicyclo[2.2.1]heptan-3-one 
• 916179-00-5 (1R,4S)-1,7,7-trimethyl-2-[2-(triphenylphospanylidene)propionyl]-2-azabicyclo[2.2.1]heptan-3-one 
• 139278-49-2 (1R,4S)-2-(4,6-Dimethyl-cyclohex-3-enecarbonyl)-1,7,7-trimethyl-2-aza-bicyclo[2.2.1]heptan-3-one 
• 250209-15-5 2-Benzyl-1,7,7-trimethyl-2-azabicyclo[2.2.1]heptane 
• 898827-35-5 (1R,4S)-2-(2-Methoxy-6-methyl-phenylethynyl)-1,7,7-trimethyl-2-aza-bicyclo[2.2.1]heptan-3-one 

Relevant academic research and scientific papers

Toward the development of a general chiral auxiliary. 9. Highly diastereoselective alkylations and acylations to form tertiary and quaternary centers.

[reaction--see text] Enolates of a new camphor-derived lactam auxiliary are shown to monoalkylate with very high diastereoselectivity. A second alkylation occurs with reactive alkylating agents to afford quaternary centers also with high diastereoselectiv