206358-46-5

Upstream product

• 112712-55-7 deux références XF130 et XF154 

Downstream Products

• 175844-90-3 (4R,5S,2'R)-3-(α-bromopropionyl)-1,5-dimethyl-4-phenylimidazolidin-2-one 
• 176018-05-6 (4R,5S,2'S)-3-(α-bromopropionyl)-1,5-dimethyl-4-phenylimidazolidin-2-one 
• 169219-76-5 (4S,5R)-1-N-(phenylacetyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one 
• 92841-65-1 (4R,5S)-1,5-dimethyl-4-phenylimidazolidin-2-one 
• 175844-92-5 (4S,5R)-1-((S)-2-Benzylamino-propionyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one 
• 176018-06-7 (4S,5R)-1-((R)-2-Benzylamino-propionyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one 
• 206358-50-1 (4R,5S)-1,5-Dimethyl-4-phenyl-3-((R)-2-piperidin-1-yl-propionyl)-imidazolidin-2-one 

Relevant academic research and scientific papers

Diastereoselective Oxidative Coupling of Enolates of Chiral Carboxylic Acid Derivatives

Enolates of chiral propionic acid amides were oxidatively dimerized with cupric salts or iodine with high simple as well as induced diastereselectivity of up to 99:1.Intramolecular coupling of chiral dienolates of 1,7-heptanediamides led to a 1,2-substituted cyclopentane and a derivative of 1,2,6,7-cyclodecane tetracarboxylic acid.