215609-78-2

Upstream product

• 40597-44-2 N-(2,2-diethoxy-ethyl)-4-methylbenzenesulfonamide 
• 215609-74-8 2-(3,4-methylenedioxyphenyl)-3-[(methoxycarbonyl)oxy]-1-cyclohexene 
• 215609-92-0 2-(3,4-methylenedioxyphenyl)-3-[(diethylphosphoryl)oxy]-1-cyclohexene 
• 335371-05-6 carbonic acid 2-benzo[1,3]dioxol-5-yl-cyclohex-2-enyl ester vinyl ester 
• 335371-06-7 2-(3,4-methylenedioxyphenyl)-3-[(isopropenyloxycarbonyl)oxy]-1-cyclohexene 
• 98-59-9 p-toluenesulfonyl chloride 
• 645-36-3 2,2-diethoxy-ethanamine 

Downstream Products

• 639-41-8 (+)-crinamine 
• 677301-64-3 (3R,3aS,7aS)-N-p-tolylsulfonyl-3-acetyloxy-3a-(3,4-methylenedioxyphenyl)-6-formyloxy-2,3,3a,6,7,7a-hexahydroindole 
• 215609-83-9 (3R,3aS,6R,7aS)-N-p-tolylsulfonyl-3-acetyloxy-3a-(3,4-methylenedioxyphenyl)-6-methoxy-2,3,3a,6,7,7a-hexahydroindole 
• 215609-85-1 (3R,3aS,6S,7aS)-N-p-tolylsulfonyl-3-acetyloxy-3a-(3,4-methylenedioxyphenyl)-6-methoxy-2,3,3a,6,7,7a-hexahydroindole 
• 215609-81-7 (3R,3aS,6R,7aS)-N-p-tolylsulfonyl-3-acetyloxy-3a-(3,4-methylenedioxyphenyl)-2,3,3a,6,7,7a-hexahydroindole 
• 677301-66-5 (3R,3aS,6S,7aS)-N-p-tolylsulfonyl-3-acetyloxy-3a-(3,4-methylenedioxyphenyl)-6-hydroxy-2,3,3a,6,7,7a-hexahydroindole 
• 215609-79-3 (3R,3aS,7aS)-N-p-tolylsulfonyl-3-acetyloxy-3a-(3,4-methylenedioxyphenyl)-2,3,3a,6,7,7a-hexahydroindole 
• 215609-76-0 (3R,3aS,7aS)-N-p-tolylsulfonyl-3-hydroxy-3a-(3,4-methylenedioxyphenyl)-2,3,3a,6,7,7a-hexahydroindole 
• 215609-75-9 N-((S)-2-Benzo[1,3]dioxol-5-yl-cyclohex-2-enyl)-4-methyl-N-(2-oxo-ethyl)-benzenesulfonamide 

Relevant academic research and scientific papers

Pd-catalyzed asymmetric allylic amination using aspartic acid derived P-chirogenic diaminophosphine oxides: DIAPHOXs

(Chemical Equation Presented) A Pd-catalyzed asymmetric allylic amination using aspartic acid derived P-chirogenic diaminophosphine oxides (DIAPHOXs) is described. Asymmetric allylic amination of both linear and cyclic substrates proceeded at room temperature to give the chiral allylic amines in 72-99% ee.