812646-66-5

Upstream product

• 267898-02-2 (E)-3-(But-2-enyloxy)-4-methoxybenzaldehyde 
• 621-59-0 isovanillin 
• 812646-63-2 2-[(2E)-but-2-enyl]-5-hydroxy-4-methoxybenzaldehyde 
• 74-88-4 methyl iodide 

Downstream Products

• 812646-69-8 1-[2-(2-butenyl)-4,5-dimethoxyphenyl]-2-propen-1-ol 
• 1391762-46-1 (E)-3-(2-(but-2-enyl)-4,5-dimethoxyphenyl)-1,5-bis(3,4,5-trimethoxyphenyl)pentane-1,5-dione 
• 1391762-48-3 (E)-4-(2-(but-2-enyl)-4,5-dimethoxyphenyl)-2,6-bis(3,4,5-trimethoxyphenyl)pyridine 
• 1391762-45-0 (E)-3-(2-(but-2-enyl)-4,5-dimethoxyphenyl)-1,5-diphenylpentane-1,5-dione 
• 1391762-47-2 (E)-4-(2-(but-2-enyl)-4,5-dimethoxyphenyl)-2,6-diphenylpyridine 
• 1414943-11-5 (E)-N-(1-(2-cinnamyl-4,5-dimethoxyphenyl)propan-2-yl)benzenesulfonamide 
• 1414943-12-6 (E)-N-(1-(2-(but-2-enyl)-4,5-dimethoxyphenyl)propan-2-yl)benzenesulfonamide 
• 1414943-18-2 3-benzenesulfonyl-7,8-dimethoxy-2-methyl-2,3-dihydro-1H-benzo[d]azepine 
• 1414942-96-3 7,8-dimethoxy-2-methyl-3-phenylsulfonyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine 
• 812646-79-0 1-[2-((E)-But-2-enyl)-4,5-dimethoxy-phenyl]-propenone 
• 10103-06-7 2,3-dimethoxynaphthalene 
• 1414943-04-6 1-but-2-enyl-4,5-dimethoxy-2-(2-nitropropenyl)benzene 

Relevant academic research and scientific papers

Synthesis of 2-hydroxymethyl-2,3-dihydrobenzofurans

A one-pot protocol toward 2-hydroxymethyl-2,3-dihydrobenzofurans (1) starting with oxygenated o-allylbenzaldehydes (3) was described. The facile one-pot process was carried out by the oxidation of o-allylbenzaldehydes (3) with Oxone in the co-solvent of acetone and DMF in the presence of aqueous EDTA solution and then intramolecular ring-closure of the resulting o-allylphenols (2) in acceptable yields.

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

Synthesis of substituted indenes from isovanillin via claisen rearrangement and ring-closing metathesis

A new synthesis of substituted indenes was studied. Based on Claisen rearrangement, Wittig reaction and ring-closing metathesis (RCM), a series of substituted indenes was synthesized from isovanillin in good yields.

A synthesis of substituted 3,6-dihydro-1H-benzo[c]oxocines via Claisen rearrangement and ring-closing metathesis

Started from isovanillin, based on Claisen rearrangement and ring-closing metathesis (RCM) reaction, a series of substituted 3,6-dihydro-1H-benzo[c]oxocines were synthesized in moderate yields.

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