863705-24-2

Upstream product

• 4962-28-1 2,5-dimethyl-4-methoxyphenol 
• 863705-22-0 2-hydroxy-5-methoxy-3,6-dimethylbenzaldehyde 
• 863705-23-1 2-hydroxy-5-methoxy-3,6-dimethylbenzenemethanol 

Downstream Products

• 863705-20-8 2-[(benzoyloxy)methyl]-3,6-dimethyl-5-pyrrolidino-2,5-cyclohexadiene-1,4-dione 
• 863705-21-9 2-[(phenylacetyloxy)methyl]-3,6-dimethyl-5-pyrrolidino-2,5-cyclohexadiene-1,4-dione 
• 863705-28-6 2-[(4-cyanobenzoyloxy)methyl]-3,6-dimethyl-5-pyrrolidino-2,5-cyclohexadiene-1,4-dione 
• 906477-65-4 2,5-dimethyl-3-[(4-cyanophenoxy)methyl]-6-pyrrolidino-2,5-cyclohexadiene-1,4-dione 
• 906477-66-5 2,5-dimethyl-3-[(4-trifluoromethylphenoxy)methyl]-6-pyrrolidino-2,5-cyclohexadiene-1,4-dione 
• 863705-25-3 2-(hydroxymethyl)-3,6-dimethyl-5-pyrrolidino-2,5-cyclohexadiene-1,4-dione 

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