1392302-95-2

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 1392302-85-0 (R)-(+)-O-[1-(4-fluorophenyl)-3-butene-1-yl]hydroxylamine 
• 879005-60-4 (S)-(-)-1-(4’-fluorophenyl)but-3-en-1-ol 
• 459-57-4 4-fluorobenzaldehyde 

Downstream Products

• 1392303-06-8 (3S,5R)-(+/-)-N-tert-butoxycarbonyl-3-(methoxycarbonylmethyl)-5-(4-fluorophenyl)isoxazolidine 
• 1392303-20-6 methyl (3S,5R)-(+)-3-(tert-butoxycarbamoyl)-5-hydroxy-5-(4-fluorophenyl)valerate 
• 1392303-25-1 tert-butyl (2R,4S)-(+)-2-(4-fluorophenyl)-6-oxotetrahydro-2H-pyran-4-yl-carbamate 

Relevant academic research and scientific papers

Stereoselective palladium-catalyzed functionalization of homoallylic alcohols: A convenient synthesis of di- and trisubstituted isoxazolidines and β-amino-δ-hydroxy esters

Enantiopure, Boc-protected alkoxyamines 12 and 13, derived from the readily available homoallylic alcohols 4 via a reaction that involves either inversion or retention of configuration, undergo a diastereoselective Pd-catalyzed ring-closing carbonylative