172796-22-4

Upstream product

• 67001-73-4 4-(tert-butyl)cyclohex-1-ene-1-carboxylic acid 
• 98-73-7 4-(1,1-dimethylethyl)benzoic acid 
• 31673-51-5 4-tert-butyl-1,5-cyclohexadiene-1-carboxylic acid 
• 76489-69-5 4-t-butyl-1,2,3,4-tetrahydrobenzoic acid 

Downstream Products

• 342894-27-3 N-<(4'-t-butylcyclohex-1'-enyl)methyl>pyrrolidine 
• 75646-66-1 4-t-butyl-1-methyl-2-methylenecyclohexabecarbaldehyde 
• 75646-68-3 cis-4-t-butyl-1-methyl-2-methylenecyclohexanecarboxylic acid 
• 75646-65-0 2-Bromomethyl-4-tert-butyl-1-methyl-cyclohexene 
• 75646-64-9 3-t-butyl-6-methyl-2,3,4,5-tetrahydrobenzyl alcohol 
• 75646-62-7 3-t-butyl-6-methyl-2,3,4,5-tetrahydrobenzaldehyde 
• 42900-72-1 5-t-butyl-2-methylcyclohexanecarbaldehyde 
• 75646-60-5 N-(4'-t-butyl-2',3',4',5'-tetrahydrobenzoyl)pyrrolidine 

Relevant academic research and scientific papers

Electroorganic reactions. Part 45. The highly stereoselective electrochemical hydrodimerisation of methyl 4-tert-butylcyclohex-1-enecarboxylate

Methyl 4-tert-butylcyclohex-1-enecarboxylate undergoes 1 F reduction at a mercury cathode in DMF solution to give as the major single product a hydrodimer in which the cyclohexyl rings are joined axially and the methoxycarbonyl groups are also axial. The

Studies on Intramolecular Alkylation. XII. Stereochemical Aspects of the Preparation of β,γ-Unsaturated Aldehydes from the -Sigmatropic Rearrangement of Ammonium Ylides

The -sigmatropic rearrangement of a series of acetonitrile-derived allylic ammonium ylides +(C4H8)-CHCN; R = 4'-t-butylcyclohexylidenemethyl (3), 4'-t-butylcyclohex-1-enyl (10), 5'-t-butyl-2'-methylcyclohex-1-enyl (14), 4'