143236-20-8

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 143236-18-4 1-((4R,5R)-4,5-Diphenyl-4,5-dihydro-isoxazol-3-yl)-but-3-en-1-ol 

Downstream Products

• 143236-21-9 3-(tert-Butyl-dimethyl-silanyloxy)-3-((4S,5S)-4,5-diphenyl-4,5-dihydro-isoxazol-3-yl)-propionaldehyde 
• 143216-91-5 3-(tert-Butyl-dimethyl-silanyloxy)-3-((4S,5S)-4,5-diphenyl-4,5-dihydro-isoxazol-3-yl)-1-phenyl-propan-1-ol 
• 143236-22-0 (R)-3-(tert-Butyl-dimethyl-silanyloxy)-3-((4S,5S)-4,5-diphenyl-4,5-dihydro-isoxazol-3-yl)-1-phenyl-propan-1-one 
• 143236-22-0 (S)-3-(tert-Butyl-dimethyl-silanyloxy)-3-((4S,5S)-4,5-diphenyl-4,5-dihydro-isoxazol-3-yl)-1-phenyl-propan-1-one 

Relevant academic research and scientific papers

Lewis Acid Promoted Stereoselective Carbon-Carbon Bond Formation of 3-Formyl-Δ2-isoxazolines

4,5-Disubstituted 3-formyl-Δ2-isoxazolines undergo the aldol, allylation, and carbonyl ene reactions in the presence of appropriate Lewis acid to give the adducts with an effective 1,3-asymmetric induction.The stereoselectivity of the reaction