69730-94-5

Upstream product

• 4801-58-5 N-hydroxypiperidine 
• 34418-91-2 2,3,4,5-tetrahydropyridine N-oxide 
• 83088-21-5 3-(β-methoxyethoxymethyloxy)-4-methoxybenzaldehyde 
• 82929-82-6 1-<3-(β-methoxyethoxymethyloxy)-4-methoxyphenyl>-3-buten-1-ol 

Downstream Products

• 66408-51-3 (+/-)-10-epi-desmethoxyabresoline 
• 53778-14-6 (+/-)-abresoline 
• 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 
• 77092-62-7 2-(p-methoxyphenylpropionoyloxy)(a)-4-(3'-hydroxy-4'-methoxyphenyl)(e)-trans-quinolizidine 
• 24806-81-3 2-(p-hydroxyphenylpropionyloxy)(a)-4-(3'-hydroxy-4'-methoxyphenyl)(e)-trans-quinolizidine 
• 77092-58-1 2-(p-MEMoxyphenylpropionoyloxy)(a)-4-(3'-MEMoxy-4'-methoxyphenyl)(e)-trans-quinolizidine 
• 77092-59-2 2-(p-methoxyphenylpropionoyloxy)(a)-4-(3'-MEMoxy-4'-methoxyphenyl)(e)-trans-quinolizidine 

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