80249-84-9

Upstream product

• 79228-13-0 10-(Cyano-methanesulfonyloxy-methyl)-9-eth-(E)-ylidene-5,6,8,9,10,11,12,13-octahydro-7,13-diaza-cyclodeca[a]indene-7-carboxylic acid phenyl ester 
• 79228-04-9 (2R,12bS)-3-Eth-(E)-ylidene-2-hydroxymethyl-2,3,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-4-one 
• 79228-10-7 6-(1,3-dithiolan-2-yl)-5-E-ethylidene-3-phenoxycarbonyl-1,2,3,4,5,6,7,8-octahydro-9H-azecino<5,4-b>indole 
• 79228-12-9 10-(Cyano-hydroxy-methyl)-9-eth-(E)-ylidene-5,6,8,9,10,11,12,13-octahydro-7,13-diaza-cyclodeca[a]indene-7-carboxylic acid phenyl ester 
• 79228-11-8 9-Eth-(E)-ylidene-10-formyl-5,6,8,9,10,11,12,13-octahydro-7,13-diaza-cyclodeca[a]indene-7-carboxylic acid phenyl ester 
• 79228-08-3 (2R,12bS)-2-[1,3]Dithiolan-2-yl-3-eth-(E)-ylidene-2,3,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-4-one 
• 79235-45-3 (2R,12bS)-2-[1,3]Dithiolan-2-yl-3-eth-(E)-ylidene-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizine 
• 79228-07-2 (2R,12bS)-3-Eth-(E)-ylidene-4-oxo-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizine-2-carbaldehyde 
• 79235-46-4 10-(Chloro-cyano-methyl)-9-eth-(E)-ylidene-5,6,8,9,10,11,12,13-octahydro-7,13-diaza-cyclodeca[a]indene-7-carboxylic acid phenyl ester 

Downstream Products

• 80249-85-0 C₂₇H₂₈N₂O₄ 
• 6393-66-4 (+/-)-epi-pleiocarpamine 
• 7240-76-8 C₂₀H₂₅N₂O⁽¹⁺⁾*I^(1-) 

Relevant academic research and scientific papers

THE TOTAL SYNTHESIS OF (+-)-C-MAVACURINE

The processes of reductive opening and oxidative reclosing of the 3,4-bond have been applied to effect overall epimerisation at C-3 in the transformation of synthetic epi-geissoschizine analogues into mavacurine-type alkaloids.