118336-75-7

Upstream product

• 87504-85-6 N-phenyl-2-<(phenylsulfonyl)methyl>propenamide 
• 118336-55-3 4-<(tert-butyldimethylsilyl)oxy>-6,10-dimethyl-N-phenyl-2-<(phenylseleno)methyl>-2,9-undecadienamide 
• 118336-40-6 4-hydroxy-6,10-dimethyl-2-methylene-N-phenyl-3-(phenylsulfonyl)-9-undecenamide 
• 118336-64-4 4-<(tert-butyldimethylsilyl)oxy>-3-hydroxy-6,10-dimethyl-2-methylene-N-phenyl-9-undecenamide 
• 106-23-0 3,7-dimethyl-oct-6-enal 
• 118336-67-7 (3R_*,4S_*)-4-<(tert-butyldimethylsilyl)oxy>-6,10-dimethyl-2-methylene-3-(mesyloxy)-N-phenyl-9-undecenamide 
• 118336-67-7 (3R_*,4R_*)-4-<(tert-butyldimethylsilyl)oxy>-6,10-dimethyl-2-methylene-3-(mesyloxy)-N-phenyl-9-undecenamide 
• 118336-46-2 4-<(tert-butyldimethylsilyl)oxy>-6,10-dimethyl-2-methylene-N-phenyl-3-(phenylsulfonyl)-9-undecenamide 

Relevant academic research and scientific papers

Dianion of N-Phenyl-2-propenamide as a Versatile Reagent for the Preparation of α-Methylene Carbonyl Compounds

A general synthetic route to α-methylene β-lactams is described that involves the regioselective electrophilic substitution of the dianion 2 generated from N-phenyl-2-propenamide (1).A convergent synthesis of conocandin N-phenylami