162599-35-1

Upstream product

• 101067-78-1 (+/-)-(3R,4S)-3-hydroxy-4-phenyl-N-(4-methoxyphenyl)azetidin-2-one 
• 2873-29-2 D-glucal triacetate 
• 783-08-4 [4-(benzylideneamino)phenyl]methanol 
• 131968-76-8 (+/-)-(3R,4S)-3-acetoxy-N-(4-methoxyphenyl)-4-phenylazetidin-2-one 

Downstream Products

• 146924-95-0 (-)-(3S,4R)-3-acetoxy-1-(4-methoxyphenyl)-4-phenylazetidin-2-one 
• 194234-99-6 Acetic acid (2S,3R,6S)-6-[(3S,4S)-1-(4-methoxy-phenyl)-2-oxo-4-phenyl-azetidin-3-yloxy]-2-methyl-3,6-dihydro-2H-pyran-3-yl ester 
• 194235-00-2 Acetic acid (2S,3R,6S)-6-[(3R,4R)-1-(4-methoxy-phenyl)-2-oxo-4-phenyl-azetidin-3-yloxy]-2-methyl-3,6-dihydro-2H-pyran-3-yl ester 
• 194235-02-4 (3S,4S)-3-hydroxy-1-(4-methoxyphenyl)-4-phenyl-2-azetidinone 
• 101067-78-1 trans-3-hydroxy-1-(4-methoxyphenyl)-4-phenylazetidin-2-one 
• 146924-91-6 (-)-cis-(3S,4R)-3-hydroxy-1-(4-methoxyphenyl)-4-phenyl-2-azetidinone 

Relevant academic research and scientific papers

Stereospecific novel glycosylation of hydroxy β-lactams via iodine-catalyzed reaction: A new method for optical resolution

Glycosylation of racemic and optically active α-hydroxy β-lactams by reaction with a few glycal derivatives in the presence of catalytic amounts of iodine has provided stereospecific formation of α-glycosides. This method has been extended for the prepara

Stereospecific Glycosylation via Ferrier Rearrangement for Optical Resolution

Diastereospecific glycosylation of racemic alcohols by reaction with suitable glycal derivatives in the presence of iodine provides easy access to both enantiomers as illustrated by the preparation of an optically pure α-hydroxy β-lactam that is an intermediate for the semisynthesis of taxol.