64566-29-6

Upstream product

• 2816-57-1 2,6-dimethylcyclohexanone 
• 26954-26-7 ethyl lithioacetate 
• 105-36-2 ethyl bromoacetate 
• 766-43-8 trans-2,6-dimethylcyclohexanone 
• 766-42-7 cis-2,6-dimethylcyclohexanone 

Downstream Products

• 91056-59-6 <2,6-Dimethyl-cyclohexen-(1)-yl-(1)>-essigsaeure 
• 61140-39-4 1-Diazo-3-(2,6-dimethyl-cyclohex-1-enyl)-propan-2-one 
• 123992-60-9 ethyl (ξ-acetoxy-2β,6β-dimethyl-1-cyclohexyl)acetate 
• 123992-69-8 ethyl (ξ-acetoxy-2β,6α-dimethyl-1-cyclohexyl)acetate 
• 123992-75-6 2-(diazoacetonylidene)-1α,3β-dimethylcyclohexane 
• 123992-71-2 ethyl (2α,6β-dimethyl-1-cyclohexylidene)acetate 
• 123992-57-4 (2α,6β-dimethyl-1-cyclohexylidene)acetic acid 
• 123992-74-5 2-(diazoacetonylidene)-1β,3β-dimethylcyclohexane 
• 123992-70-1 ethyl (2β,6β-dimethyl-1-cyclohexylidene)acetate 
• 123992-56-3 (2β,6β-dimethyl-1-cyclohexylidene)acetic acid 
• 61346-66-5 ethyl 2,6-dimethyl-1-cyclohexeneacetate 

Relevant academic research and scientific papers

A Direct Retro-Reformatsky Fragmentation: Formal Ring Enlargement of Cyclic Ketones for Novel and Practical Synthesis of Heterocyclic Enamines

A novel and practical synthesis of heterocyclic enamines has been developed from the formal ring enlargement of cyclic ketones, which comprised the retro-Reformatsky fragmentation reaction as a key step. Under alkaline bromination conditions, the Reformat

A New, General Cyclopentenone Synthesis

A new synthesis of cyclopentenones, involving an Rh(II)-catalyzed, intramolecular carbon-hydrogen insertion of diazomethyl ketones derived from α,β-unsaturated acids, is described.