823787-97-9

Upstream product

• 1779-49-3 Methyltriphenylphosphonium bromide 
• 823787-92-4 tert-butyl((1R,2S,5S)-5-{[tert-butyl(dimethyl)silyl]oxy}-2-methyl-3-oxocyclopentyl)methyl[(4-methylphenyl)sulfonyl]carbamate 
• 823787-96-8 N-(2-iodo-allyl)-4-methyl-N-(5-methyl-4-oxo-cyclopent-2-enylmethyl)-benzenesulfonamide 
• 823787-94-6 4-methyl-N-(5-methyl-4-oxo-cyclopent-2-enylmethyl)-N-prop-2-ynyl-benzenesulfonamide 
• 823787-93-5 4-methyl-N-{[(1R,5S)-5-methyl-4-oxo-2-cyclopenten-1-yl]methyl}benzenesulfonamide 
• 823787-91-3 (2S,3R,4S)-4-{[tert-butyl(dimethyl)silyl]oxy}-3-(hydroxymethyl)-2-methylcyclopentanone 
• 823788-10-9 (1S,2S,5S)-5-{[tert-butyl(dimethyl)silyl]oxy}-2-methyl-3-oxocyclopentanecarbaldehyde 
• 18303-04-3 N-[(tert-butoxy)carbonyl]-4-methylbenzenesulfonamide 
• 56745-67-6 (4S)-4-tert-butyldimethylsilyloxycyclopent-2-en-1-one 
• 950479-64-8 (4S,4aS,6S,7S,7aS)-6-benzyloxy-7-methyl-2-(p-toluenesulfonyl)-octahydro-1H-cyclopenta[c]pyridin-4-ol 
• 950479-63-7 (4S,4aS,6S,7S,7aS)-6-benzyloxy-4-methoxymethoxy-7-methyl-2-(p-toluenesulfonyl)octahydro-1H-cyclopenta[c]pyridine 
• 950479-62-6 (4S,4aS,6S,7S,7aS)-4-methoxymethoxy-7-methyl-2-(p-toluenesulfonyl)octahydro-1H-cyclopenta[c]pyridin-6-ol 
• 950479-60-4 (4S,6R,7S,7aS)-4-methoxymethoxy-7-methyl-2-(p-toluenesulfonyl)-1,2,3,4,7,7a-hexahydro-1H-cyclopenta[c]pyridin-6-ol 
• 950479-56-8 (4S,7S,7aS)-4-methoxymethoxy-7-methyl-2-(p-toluenesulfonyl)-1,2,3,4,7,7a-hexahydro-6H-cyclopenta[c]pyridin-6-one 

Downstream Products

• 823788-09-6 bis[(4R,4aS,6R,7S,7aR)-2,4,7-trimethyloctahydro-1H-cyclopenta[c]pyridin-6-yl] 2,4-bis(3-methoxy-4-{[(4-methylphenyl)sulfonyl]oxy}phenyl)cyclobutane-1,3-dicarboxylate 
• 823788-03-0 (4R,4aS,6R,7S,7aR)-2,4,7-trimethyloctahydro-1H-cyclopenta[c]pyridin-6-yl 4-nitrobenzoate 
• 145307-22-8 (4R,4aS,6R,7S,7aR)-2,4,7-trimethyloctahydro-1H-cyclopenta[c]pyridin-6-ol 
• 823787-98-0 (4aR,6S,7S,7aR)-6-{[tert-butyl(dimethyl)silyl]oxy}-7-methyl-4-methylene-2-[(4-methylphenyl)sulfonyl]octahydro-1H-cyclopenta[c]pyridine 

Relevant academic research and scientific papers

Diastereoselective formal synthesis of a monoterpene alkaloid, (-)-incarvilline

(Chemical Equation Presented) Diastereoselective formal synthesis of a monoterpene alkaloid, (-)-incarvilline, the key intermediate for the synthesis of (-)-incarvillateine, was achieved by using an intramolecular Pauson-Khand reaction of (5)-N-[(E)-2-but

Total synthesis of (-)-incarvilline, (+)-incarvine C, and (-)-incarvillateine

The first total syntheses of new monoterpene alkaloids (-)-incarvilline, (+)-incarvine C, and (-)-incarvillateine, corresponding to the natural enantiomers, have been accomplished. The strategy for the synthesis of these natural products utilized 6-epi-in