80324-11-4

Upstream product

• 106-95-6 allyl bromide 
• 6346-05-0 3-benzyloxy-4-methoxybenzaldehyde 

Downstream Products

• 1449790-36-6 2-[3-(benzyloxy)-4-methoxyphenyl]-2-methyl-2,3,4,5-tetrahydro-1-benzoxepine 
• 1449790-25-3 2-[3-(benzyloxy)-4-methoxyphenyl]-2,3,4,5-tetrahydro-1-benzoxepine 
• 1449790-08-2 2-[3-(benzyloxy)-4-methoxyphenyl]-5-(2-bromophenyl)pentan-2-ol 
• 1449789-98-3 1-[3-(benzyloxy)-4-methoxyphenyl]-4-(2-bromophenyl)butan-1-ol 
• 1449789-88-1 1-[3-(benzyloxy)-4-methoxyphenyl]-4-(2-bromophenyl)butan-1-one 
• 24806-77-7 (2R,4R,9aS)-4-(3-Benzyloxy-4-methoxy-phenyl)-octahydro-quinolizin-2-ol 
• 24806-77-7 (2S,4R,9aR)-4-(3-Benzyloxy-4-methoxy-phenyl)-octahydro-quinolizin-2-ol 
• 24806-77-7 (2R,4R,9aR)-4-(3-Benzyloxy-4-methoxy-phenyl)-octahydro-quinolizin-2-ol 
• 52656-92-5 (2R,4R,9aS)-4-(3-Hydroxy-4-methoxy-phenyl)-octahydro-quinolizin-2-ol 
• 52656-92-5 (2R,4R,9aR)-4-(3-Hydroxy-4-methoxy-phenyl)-octahydro-quinolizin-2-ol 
• 80324-15-8 Benzoic acid (2R,4R,9aR)-4-(3-benzyloxy-4-methoxy-phenyl)-octahydro-quinolizin-2-yl ester 
• 57907-27-4 Acetic acid (2R,4R,9aR)-4-(3,4-dimethoxy-phenyl)-octahydro-quinolizin-2-yl ester 
• 89771-49-3 (±)-lasubine II 

Relevant academic research and scientific papers

Transition metals catalyzed C-C and C-O bonds formation: Facile synthesis of flavans and benzoxepines

A simple and practical method has been developed based on intermolecular [Pd]-catalyzed C-C and an intramolecular [Cu]-catalyzed C-O bond formations for the synthesis of flavans and benzoxepines. Interestingly, the method is amenable for the synthesis of

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