82929-82-6

Upstream product

• 83088-21-5 3-(β-methoxyethoxymethyloxy)-4-methoxybenzaldehyde 
• 106-95-6 allyl bromide 

Downstream Products

• 82929-83-7 2-(2S,3aR)-Hexahydro-isoxazolo[2,3-a]pyridin-2-yl-1-[4-methoxy-3-(2-methoxy-ethoxymethoxy)-phenyl]-ethanol 
• 69730-94-5 (2R,4R,9aS)-4-[4-Methoxy-3-(2-methoxy-ethoxymethoxy)-phenyl]-octahydro-quinolizin-2-ol 
• 69730-94-5 (2S,4R,9aR)-4-[4-Methoxy-3-(2-methoxy-ethoxymethoxy)-phenyl]-octahydro-quinolizin-2-ol 
• 69730-96-7 (E)-3-[3-Methoxy-4-(2-methoxy-ethoxymethoxy)-phenyl]-acrylic acid (2R,4R,9aR)-4-[4-methoxy-3-(2-methoxy-ethoxymethoxy)-phenyl]-octahydro-quinolizin-2-yl ester 
• 96421-70-4 (E)-3-[4-(2-Methoxy-ethoxymethoxy)-phenyl]-acrylic acid (2R,4R,9aS)-4-[4-methoxy-3-(2-methoxy-ethoxymethoxy)-phenyl]-octahydro-quinolizin-2-yl ester 
• 66408-51-3 (+/-)-10-epi-desmethoxyabresoline 
• 53778-14-6 (+/-)-abresoline 

Relevant academic research and scientific papers

Synthetic Studies on Lythraceae Alkaloids via Cycloaddition. I. Total Synthesis of Some Simple Phenylquinolizidine Alkaloids and Ester Alkaloids 1,2)

A general synthetic route to Lythraceae alkaloids based on a regio- and stereoselective cycloaddition reaction has been developed.The cycloaddition of the nitrone 5 with the olefins 14 and 26 gave the adducts 15 and 27 which, upon treatment with