812646-71-2

Upstream product

• 621-59-0 isovanillin 
• 812646-63-2 2-[(2E)-but-2-enyl]-5-hydroxy-4-methoxybenzaldehyde 
• 267898-02-2 (E)-3-(But-2-enyloxy)-4-methoxybenzaldehyde 
• 1826-67-1 vinyl magnesium bromide 
• 812646-68-7 5-(benzyloxy)-2-(but-2-enyl)-4-methoxybenzaldehyde 

Downstream Products

• 812646-81-4 1-[5-Benzyloxy-2-((E)-but-2-enyl)-4-methoxy-phenyl]-propenone 
• 79928-74-8 2-(benzyloxy)-3-methoxynaphthalene 

Relevant academic research and scientific papers

Syntheses of substituted naphthalenes and naphthols

Syntheses of substituted naphthalenes and naphthols are described. Based on Claisen rearrangement, ring-closing metathesis (RCM), and related reactions, isovanillin was successfully transformed into a series of substituted naphthalenes and naphthols with

A novel synthesis of substituted naphthalenes via Claisen rearrangement and RCM reaction

A novel synthesis of substituted naphthalenes was studied. Starting from isovanillin, basing on Claisen rearrangement and ring-closing metathesis (RCM), a series of 1-alkoxy-2-methoxynaphthalenes and 1-alkoxy-2-methoxy-8-methylnaphthalenes together with a