852202-18-7

Upstream product

• 139437-47-1 (R)-2-{[1-Furan-2-yl-meth-(E)-ylidene]-amino}-2-phenyl-ethanol 
• 106-95-6 allyl bromide 
• 56613-80-0 D-2-phenylglycinol 
• 98-01-1 furfural 

Downstream Products

• 936227-00-8 (R)-3-[(R)-1-(furan-2-yl)but-3-enyl]-4-phenyloxazolidin-2-one 

Relevant academic research and scientific papers

Asymmetric synthesis of di- and trisubstituted pyrrolidinones via zirconium-mediated intramolecular coupling of N-3-alkenyl carbamates

N-3-Alkenyl carbamates, which are readily available in enantiomerically pure form, undergo a stereoselective intramolecular coupling under the effect of a Cp2ZrCl2/2n-BuLi reagent. The influence of the carbamate structure on the ster

Indium-mediated asymmetric barbier-type allylation of aldimines in alcoholic solvents: Synthesis of optically active homoallylic amines

(Chemical Equation Presented) Chiral aldimines derived from phenylglycinol were diastereoselectively allylated with indium powder/allyl bromide in alcoholic solvents. Both aliphatic and aromatic aldimines provided good yield of the desired products with h