836596-29-3

Upstream product

• 91-13-4 α,α'-dibromo-o-xylene 
• 93-91-4 1-phenylbutan-1,3-dione 

Downstream Products

• 91142-58-4 2,3-dihydro-2-methyl-1H-indene-2-carboxylic acid 
• 125866-03-7 2-phenyl-2,3-dihydro-1H-indene-2-carboxylic acid 
• 836596-53-3 C₂₆H₂₈O₄ 
• 836596-51-1 C₂₆H₂₈O₄ 
• 836596-49-7 C₂₄H₂₄O₄ 
• 836596-47-5 C₂₄H₂₄O₄ 
• 836596-45-3 C₂₃H₂₂O₄ 
• 836596-43-1 C₂₃H₂₂O₄ 

Relevant academic research and scientific papers

Mechanism and regioselectivity of the anionic oxidative rearrangement of 1,3-diketones towards all-carbon quaternary carboxylates

The oxidative rearrangement of 1,3-diketones is an underexplored alternative to enolate chemistry in the synthesis of all-carbon quaternary carboxylates. The mechanistic investigation of this reaction has resulted in a mild base mediated protocol, whose r

Synthesis of spiro[5.4]decenones and their transformation into bicyclo[4.4]deca-1,4-dien-3-ones by domino "elimination-double-Wagner- Meerwein-rearrangement" reactions

The [3+3] cyclization of 1,3-bis-silyl enol ethers with 1,1-diacylcyclopentanes allows a convenient synthesis of spiro[5.4]decenones. Treatment of these compounds with trifluoroacetic acid (TFA) afforded a great variety of bicyclo[4.4.0]deca-1,4-dien-3-on