76509-18-7

Upstream product

• 3389-21-7 3-(2-bromoethyl)-1H-indole 
• 76509-17-6 3-benzyloxypyridine 

Downstream Products

• 76509-20-1 5-Benzyloxy-1-[2-(1H-indol-3-yl)-ethyl]-1,2,3,6-tetrahydro-pyridine-2-carbonitrile 
• 76509-19-8 3-[2-(5-Benzyloxy-3,6-dihydro-2H-pyridin-1-yl)-ethyl]-1H-indole 
• 76509-21-2 3-benzyloxy-1,4,6,7,12,12b-hexahydroindolo<2,3-a>quinolizine 
• 56491-03-3 (+/-)-deplancheine 
• 114495-24-8 3-[2-(5-Benzyloxy-6-cyano-3,6-dihydro-2H-pyridin-1-yl)-ethyl]-indole-1-carboxylic acid tert-butyl ester 
• 114495-25-9 3-[2-(5-Benzyloxy-3,6-dihydro-2H-pyridin-1-yl)-ethyl]-indole-1-carboxylic acid tert-butyl ester 
• 114495-23-7 3-Benzyloxy-1-[2-(1H-indol-3-yl)-ethyl]-1,2,5,6-tetrahydro-pyridine-2-carbonitrile 

Relevant academic research and scientific papers

A total synthesis of the alkaloid deplancheine

The indole alkaloid deplancheine (1) has been synthesised utilising a Witting reaction on the octahydro[2,3-a]quinolizin-2-one (2) itself available in four synthetic steps from readily available materials.

NOVEL APPLICATIONS OF THE MODIFIED POLONOVSKI REACTION - IX A NEW ROUTE TO WENKERT'S ENAMINE

A practical synthetic entry to Wenkert's enamine 1 employing the modified Polonovski reaction is described.Complete 13 C NMR spectral data of 1 is presented.Conformational analysis of the intermediate 1-hydroxy- and 1-ethyl-1-hydroxy-indoloquinolizidines