161465-54-9

Upstream product

• 91-00-9 Benzhydrylamine 

Downstream Products

• 161465-61-8 (4R)-1-diphenylmethyl-4-p-tolylsulfanylazetidin-2-one 
• 171015-56-8 (3S,4R)-1-diphenylmethyl-3-ethyl-4-p-tolylsulfinylazetidin-2-one 
• 171015-55-7 (3S,4R)-1-diphenylmethyl-3-ethyl-4-p-tolylsulfanylazetidin-2-one 
• 171231-53-1 (3R,4R)-1-diphenylmethyl-3-ethyl-4-methoxycarbonylmethylazetidin-2-one 
• 171015-57-9 (3R,4R)-1-diphenylmethyl-3-ethyl-4-hydroxyethylazetidin-2-one 

Relevant academic research and scientific papers

A highly asymmetric Pummerer-type cyclization of chiral, non-racemic β-amidosulfoxides induced by O-silylated ketene acetals

The first highly asymmetric Pummerer-type cyclization of chiral, non-racemic β-amidosulfoxides leading to enantiomerically enriched β-lactams (80-85% ee) is described. S- and R-sulfoxides (S-2a-d and R-2a-c) were treated with O-methyl-O-tert-butyldimethyl

Highly asymmetric Pummerer-type cyclization of chiral, non-racemic β-amido sulfoxides

The first highly asymmetric Pummerer-type cyclization of chiral, non-racemic β-amido sulfoxides to enantiomerically enriched β-lactams (80-85percent ee) is described.S- and R-Silfoxides (S-2a-d and R-2a-c) were treated with O-methyl-O-tert-butyldimethylsi