327615-03-2

Upstream product

• 104129-40-0 2,5-dimethoxy-3,6-dimethylbenzaldehyde 
• 137-18-8 2,5-Dimethyl-1,4-benzoquinone 
• 4885-02-3 Dichloromethyl methyl ether 
• 2674-32-0 1,4-dimethoxy-2,5-dimethylbenzene 
• 4962-28-1 2,5-dimethyl-4-methoxyphenol 
• 863705-22-0 2-hydroxy-5-methoxy-3,6-dimethylbenzaldehyde 

Downstream Products

• 863705-27-5 2,5-dimethyl-3-(phenoxymethyl)-2,5-cyclohexadiene-1,4-dione 
• 863705-26-4 1-(phenoxymethyl)-2,5-dimethoxy-3,6-dimethylbenzene 
• 863705-15-1 2,5-dimethyl-3-(phenoxymethyl)-6-pyrrolidino-2,5-cyclohexadiene-1,4-dione 
• 91244-98-3 1-chloromethyl-2,5-dimethoxy-3,6-dimethylbenzene 

Relevant academic research and scientific papers

Photoactivation of amino-substituted 1,4-benzoquinones for release of carboxylate and phenolate leaving groups using visible light

Upon exposure to visible light, 2-pyrrolidino-substituted 3,6-dimethyl-1,4-benzoquinones photocyclize to give benzoxazolines with quantum yields of 0.07-0.10 in CH2Cl2, 0.02-0.04 in CH 3CN, and 3/su

Photochemical cyclization with release of carboxylic acids and phenol from pyrrolidino-substituted 1,4-benzoquinones using visible light

(Chemical Equation Presented) Visible light irradiation of 5-acyloxymethyl- and 5-phenoxymethyl-2-pyrrolidino-1,4-benzoquinones effects photoisomerization to labile oxazolidines, which undergo elimination of carboxylate or phenolate leaving groups in high

TRICYCLIC DIHYDROBENZOFURAN DERIVATIVES, PROCESS FOR THE PREPARATION THEREOF AND AGENTS

A compound represented by the formula: wherein Ring A is a non-aromatic 5- to 7-membered nitrogen-containing heterocyclic ring which may be further substituted, Ring B is benzene ring which is further substituted, Ring C is a dihydrofuran ring which may b