246521-95-9

Upstream product

• 1333161-29-7 C₂₂H₃₂N₂O₅S 
• 1333161-21-9 C₂₅H₄₀N₂O₅SSi 
• 1333161-18-4 C₁₇H₂₄N₂O₃S 
• 246521-93-7 C₂₈H₂₆N₂O₄ 
• 246521-92-6 (4R,5R)-4-(allylbenzyloxycarbonylaminomethyl)-2-[4-(benzyloxy)phenyl]-5-vinyl-1,3-oxazoline 
• 246521-91-5 (4R,5R)-4-(benzyloxycarbonylaminomethyl)-2-[4-(benzyloxy)phenyl]-5-vinyl-1,3-oxazoline 
• 246521-90-4 (4R,5R)-2-[4-(benzyloxy)phenyl]-4-(azidomethyl)-5-vinyl-1,3-oxazoline 
• 246521-89-1 (4R,5R)-2-[4-(benzyloxy)phenyl]-4-(hydroxymethyl)-5-vinyl-1,3-oxazoline 
• 246521-88-0 (4R,5R)-2-[4-(benzyloxy)phenyl]-4-[(tert-butyldimethylsilanyloxy)methyl]-5-vinyl-1,3-oxazoline 

Downstream Products

• 158584-98-6 4-hydroxy-3-[4-(phenylmethoxy)benzoylamino]-1-(phenylmethoxycarbonyl)-hexahydroazepine 

Relevant academic research and scientific papers

Stereoselective synthesis of syn-β-amino propargylic ethers: Application to the asymmetric syntheses of (+)-β-conhydrine and (-)-balanol

The stereoselective synthesis of syn-β-amino propargylic ethers by the addition of racemic lithio 3-(methoxymethoxy)allenylcuprates, and more particularly (cyano) and (mesityl)cuprates, to enantiopure chiral N-tert-butylsulfinylimines is reported. The sco

Asymmetric synthesis of the balanol heterocycle via a palladium-mediated epimerization and olefin metathesis.

[formula: see text] The enantioselective formal synthesis of balanol, a potent protein kinase C inhibitor, was accomplished from D-serine utilizing a Pd-catalyzed equilibration of diastereomeric 5-vinyloxazolines to set the stereochemistry of the vicinal