851-36-5

Upstream product

• 35227-78-2 diethyl (ethoxymagnesio)malonate 
• 3535-37-3 3,4-dimethoxybenzoic acid chloride 
• 93-07-2 Veratric acid 
• 105-53-3 diethyl malonate 

Downstream Products

• 53979-19-4 diethyl 2-(3,4-dimethoxybenzyl)malonate 
• 4687-37-0 ethyl 3,4-dimethoxybenzoylacetate 
• 1131-62-0 1-(3,4-dimethoxyphenyl)ethanone 
• 114855-49-1 diethyl α-bromo-3,4-dimethoxybenzylmalonate 
• 4687-40-5 threo-diethyl 2,3-bis-(3,4-dimethoxybenzoyl)butane-1,4-dioate 
• 72536-39-1 threo-2,3-bis-(α-hydroxy-3,4-dimethoxybenzyl)butane-1,4-diol 
• 944329-82-2 C₂₆H₂₈O₁₀ 

Relevant academic research and scientific papers

Simple synthesis of eudesmin through oxidative coupling of carbanions and reductive catalytic hydrogenation of diketo diester

A simple synthesis of eudesmin (1) is described. The key fragments were diol 13, dicarbethoxyethane 4, and diketo diester 5, which were prepared via reductive catalytic hydrogenation and oxidative intermolecular coupling of carbanions. This method is useful to generate the core skeleton of an endo-endo furofuran ring. Copyright Taylor & Francis Group, LLC.

BENZOPHENANTHRIDINES V. INVESTIGATION OF THE RODIONOV-SUVOROV SCHEME. SYNTHESIS OF 3,3-DIETHOXYCARBONYL-2-(3,4-DIMETHOXYPHENYL)-6,7-DIMETHOXY-1-TETRALONE

Triethyl 1,3-bis(3,4-dimethoxyphenyl)propane-1,2,2-tricarboxylate was synthesized by the alkylation of the lithium enolate of ethyl homoveratrate with α-bromo(3,4-dimethoxybenzyl)malonic ester.It was converted by intramolecular acylation, catalyzed by BF3