133056-52-7

Upstream product

• 133056-49-2 (+)-(4S,5S)-4-(Methoxymethyl)-5-phenyl-2-(1,4,5-trimethoxy-2-naphthyl)-4,5-dihydroxooxazole 
• 134276-82-7 2-(2-bromo-3,5-dimethoxy-phenyl)-[1,3]dioxolane 
• 134276-83-8 2-(2-bromo-3,5-dimethoxyphenyl)-5,5-dimethyl-1,3-dioxane 
• 123796-58-7 1,4,5-Trimethoxynaphthalene-2-carbonitrile 
• 134276-84-9 2-(3-benzyloxy-2-bromo-5-methoxyphenyl)-1,3-dioxane 
• 134276-85-0 2-(3-benzyloxy-2-bromo-5-methoxyphenyl)-5,5-dimethyl-1,3-dioxane 
• 133056-50-5 2-(2-Bromo-3,5-dimethoxyphenyl)-1,3-dioxane 

Downstream Products

• 133056-49-2 (+)-(4S,5S)-4-(Methoxymethyl)-5-phenyl-2-(1,4,5-trimethoxy-2-naphthyl)-4,5-dihydroxooxazole 

Relevant academic research and scientific papers

Synthetic Approaches to the Naphthyl-isoquinoline Alkaloids. Part 2. The Total Synthesis of (-)-O-Methylancistrocladine and (+)-O-Methylhamatine and their Enantiomers

An asymmetric total synthesis of the naphthyl-isoquinoline alkaloids (-)-O-methylancistrocladine 39 is described; the synthetic method also provides routes to the atropisomer (+)-O-methylhamatine 43 and the enantiomers of these alkaloids.The asymmetric co

Synthetic Approaches to the Alkaloids of the Ancistrocladaceae. Part 3. The Total Synthesis of (-)-Ancistrocladinine: Control of the Diastereoisomer Excess in the Synthesis of Axially Chiral Biaryls.

The total synthesis of the naphthylisoquinoline alkaloid (-)-ancistrocladinine is described.The key step was the construction of the disymmetric bi