62733-86-2

Upstream product

• 64-18-6 formic acid 
• 33235-14-2 1-methyl-3-oxocyclohexane-1-carbonitrile 
• 1193-18-6 3-methylcyclohexen-2-one 
• 124-38-9 carbon dioxide 
• 151-50-8 potassium cyanide 
• 56294-19-0 methyl 1-methyl-3-oxocyclohexane-1-carboxylate 

Downstream Products

• 56840-25-6 (1S,3S)-3-(4-Methoxy-phenyl)-1-methyl-cyclohexanecarboxylic acid methyl ester 
• 56840-25-6 (1S,3R)-3-(4-Methoxy-phenyl)-1-methyl-cyclohexanecarboxylic acid methyl ester 
• 56840-21-2 1-methyl-t-3-p-methoxyphenylcyclohexane-r-1-carboxylic acid 
• 56840-21-2 1-methyl-c-3-p-methoxyphenylcyclohexane-r-1-carboxylic acid 
• 56840-28-9 5-methyl-1-phenylbicyclo<3.2.1>octan-6-one 
• 56840-24-5 (1S,3R)-1-Methyl-3-phenyl-cyclohexanecarboxylic acid methyl ester 
• 56840-19-8 1-methyl-c-3-phenylcyclohexane-r-1-carboxylic acid 
• 91513-01-8 ethyl 3-methoxycarbonyl-3-methyl-1-(p-methoxyphenyl)cyclohexylcyanoacetate 
• 90995-42-9 ethyl 3-methoxycarbonyl-3-methyl-1-phenylcyclohexylcyanoacetate 
• 344552-43-8 methyl 3-methoxycarbonyl-3-methyl-1-(p-methoxyphenyl)cyclohexylacetate 
• 344868-51-5 methyl 3-methoxycarbonyl-3-methyl-1-phenylcyclohexylacetate 
• 90995-41-8 ethyl 3-methoxycarbonyl-3-methylcyclohexylidenecyanoacetate 
• 90995-60-1 (1S,5R)-7-[1-Hydroxy-meth-(E)-ylidene]-1-(4-methoxy-phenyl)-5-methyl-bicyclo[3.2.1]octan-6-one 
• 56840-23-4 c-3-hydroxy-1-methyl-t-3-p-methoxyphenylcyclohexane-r-1,3-carbolactone 

Relevant academic research and scientific papers

Chemical Transformation of Terpenoids. VII. Syntheses of Chiral Segments, Key Building-Blocks for the Right Half of Taxane-Type Diterpenoids

Two kinds of chiral segments, i.e. segment B-I (4) and segment B-II (5), which are potentially versatile building-blocks for construction of the right half of taxane-type diterpenoids, were synthesized from 3-methyl-2-cyclohexen-1-one (6) via optical reso

Regioselectivity in the Intramolecular Carbon-Hydrogen Insertion in Metal-catalysed Decomposition of some cis-1-Methyl-3-arylcyclohexyl Diazomethyl Ketones. A Highly Efficient Homogeneous Nickel Catalyst for Carbenoid Insertion

The comparative effectiveness of a variety of copper catalysts and a few transition-metal chelates have been examined in the carbenoid decomposition of cis,cis-1,5-dimethyl-3-phenylcyclohexyl diazomethyl ketone (11),

ELECTROCHEMICAL CARBOXYLATION OF alpha , beta -UNSATURATED KETONES WITH CARBON DIOXIDE.

Several aromatic and aliphatic alpha , beta -unsaturated ketones were converted to the corresponding gamma -keto acids by the electrochemical reduction in acetonitrile in the presence of CO//2. The yields of the keto acid were 73-82% when the enones have at least one aromatic substituent. In the case of aliphatic enones, the yields of the carboxylation reaction were 67% for 2-cyclohexen-1-one and 44% for 3-buten-2-one.