72402-47-2

Upstream product

• 56-54-2 (6-Methoxy-quinolin-4-yl)-((1S,2S,4S,5R)-5-vinyl-1-aza-bicyclo[2.2.2]oct-2-yl)-methanol 
• 908578-83-6 N-bromoquinotoxine 
• 56-54-2 quinindine 

Downstream Products

• 130-95-0 quinine 
• 56-54-2 quinine 
• 1393601-64-3 (8R,9S)-6'-methoxy-9-phenyl-9-cinchonanol 
• 1393601-69-8 (8S,9R)-6'-methoxy-9-phenyl-9-cinchonanol 
• 1393601-66-5 (8R,9S)-6'-methoxy-9-(3-aminophenyl)-9-cinchonanol 

Relevant academic research and scientific papers

Rabe rest in peace: Confirmation of the rabe-kindler conversion of d-quinotoxine into quinine: Experimental affirmation of the woodward-doering formal total synthesis of quinine

(Chemical Equation Presented) Put to rest: The three-step conversion of d-quinotoxine into quinine, as originally reported by Rabe and Kindler in 1918, has been experimentally verified. This conversion serves to reaffirm the formal total synthesis of quin

Synthetic approaches to 9-arylated Cinchona alkaloids: Stereoselective addition of Grignard reagents to cinchonanones and hydroxylation of 9-phenylcinchonanes

All 8,9-isomers of the 9-phenyl Cinchona alkaloids were obtained by autoxidation of 9-deoxy-9-phenyl-alkaloids and by the addition of Grignard reagents to the respective ketones. The diastereoselective addition of phenyl-, methyl-, and vinylmagnesium reag

Barium Permanganate, Ba(MnO4)2; An Efficient and Mild Oxidizing Agent for Use Under Non-aqueous and Aprotic Conditions

Barium permanganate is used for the efficient oxidation of different types of alcohols and acyloins to the corresponding carbonyl compounds in boiling acetonitrile.The mildness of this reagent is shown by the oxidative S,S-coupling of several thiols to disulfides.