778591-61-0

Upstream product

• 1666-13-3 diphenyl diselenide 
• 778591-57-4 (6R,12bS)-12-(tert-butoxycarbonyl)-1,2,3,4,6,7,12,12b-octahydro-4-oxoindolo[2,3-a]quinolizine-6-carboxylic acid 
• 6026-86-4 methyl 4-formylbutanoate 
• 24424-99-5 di-tert-butyl dicarbonate 
• 153-94-6 D-tryptophan 
• 778591-60-9 (6R,12bS)-tert-butyl-6-formyl-1,2,3,4,6,7-hexahydro-4-oxoindolo[2,3-a]quinolizine-12(12bH)-carboxylate 
• 778591-56-3 (6R,12bS)-1,2,3,6,7,12b-hexahydro-6-(hydroxymethyl)indolo[2,3-a]quinolizin-4(12H)-one 
• 778591-59-6 (6R,12bS)-4-oxo-1,2,3,4,6,7,12,12b-octahydropyrido[2,1-a]β-carboline-6-carbaldehyde 
• 154-09-6 (2R)-2-amino-3-(1H-indol-3-yl)propan-1-ol 

Relevant academic research and scientific papers

A highly stereoselective synthesis of the indolo[2,3-a]quinolizine ring system and application to natural product synthesis

We present a facile and highly stereoselective approach to the indolo[2,3-a]quinolizine ring system from a readily available, non-racemic chiral template. We demonstrate the potential for application of this methodology to natural product synthesis throug

An asymmetric synthesis of both enantiomers of the indole alkaloid deplancheine

(Chemical Equation Presented). We report a novel, facile and asymmetric approach to both enantiomers of the indole alkaloid deplancheine from a readily available, nonracemic chiral template. The natural product and its antipode are isolated with >95% ee.