135405-09-3

Upstream product

• 67-56-1 methanol 
• 383-83-5 2-methyl-3-chloropropanoylfluoride 

Downstream Products

• 142699-41-0 1-methoxy-1-ethenyl-2-(1'-hydroxy-2'-methylprop-2'-en-1'-yl)cyclohexane 
• 142699-41-0 1-methoxy-1-ethenyl-2-(1'-hydroxy-2'-methylprop-2'-en-1'-yl)cyclohexane 
• 142699-41-0 1-methoxy-1-ethenyl-2-(1'-hydroxy-2'-methylprop-2'-en-1'-yl)cyclohexane 
• 142699-41-0 1-methoxy-1-ethenyl-2-(1'-hydroxy-2'-methylprop-2'-en-1'-yl)cyclohexane 
• 135405-10-6 1-methoxy-1-ethynyl-2-(2'-methyl-1'-oxoprop-2'-enyl)cyclohexane 
• 135405-10-6 1-methoxy-1-ethynyl-2-(2'-methyl-1'-oxoprop-2'-enyl)cyclohexane 
• 135405-10-6 1-(2-Ethynyl-2-methoxy-cyclohexyl)-2-methyl-propenone 

Relevant academic research and scientific papers

The sequence of a stepwise Ade reaction and intramolecular Pauson-Khand cycloaddition as an entry into the synthesis of polycyclic compounds

A stepwise AdE acylmethoxylation across the double bond of dicobalt hexacarbonyl complexes (DCHCC) of conjugated enynes was elaborated as an efficient and general route for the synthesis of DCHCC of 1,6-enynes containing a combination of five-

An unusual case of Khand-Pauson cyclization involving the participation of a conjugated double bond. A promising sequence for the assemblage of polycyclic framework

A short and convergent route for the synthesis of polycyclic linearly and/or angularly fused compounds is proposed based on the intramolecular alkyne-alkene-carbonyl cycloaddition with participation of the double bond bearing an electron withdrawing group