127129-06-0

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 491-07-6 (+/-)-menthone 
• 412324-05-1 C₁₀H₁₈O 
• 3391-87-5 l-menthone 

Downstream Products

• 139016-72-1 C₄₀H₆₆O₅ 
• 139016-71-0 (2R,3R,4S,5S,6S)-5-Benzyloxy-6-((2S,3S,6S,7R,10S)-7-isopropyl-3,10-dimethyl-1,5-dioxa-spiro[5.5]undec-2-yl)-2,4-dimethyl-heptane-1,3-diol 
• 139016-71-0 (2S,3S,4R,5R,6R)-5-Benzyloxy-6-((2R,3R,6R,7R,10S)-7-isopropyl-3,10-dimethyl-1,5-dioxa-spiro[5.5]undec-2-yl)-2,4-dimethyl-heptane-1,3-diol 
• 3391-87-5 l-menthone 
• 929033-28-3 (2S,3S,6R)-2-bromo-3-methyl-6-(prop-2-yl)-cyclohexanone 
• 105367-46-2 ((3S,6S)-6-Isopropyl-3-methyl-cyclohex-1-enyloxy)-trimethyl-silane 
• 74185-00-5 (3R,6S)-3-methyl-6-(prop-2-yl)-1-trimethylsilyloxy-cyclohexene 
• 89-80-5 p-menthan-2-one 
• 105252-07-1 r-2,t-3-Dimethyl-c-6-(1-methylethyl)-1-cyclohexanon 
• 105252-08-2 r-2,c-3-Dimethyl-c-6-(1-methylethyl)-1-cyclohexanon 
• 946524-55-6 t-3-Methyl-c-6-(1-methylethyl)-r-2-(2-propenyl)-1-cyclohexanon 
• 105252-10-6 c-3-Methyl-c-6-(1-methylethyl)-r-2-(2-propenyl)-1-cyclohexanon 
• 59781-56-5 1--1-ethanon 
• 68298-49-7 (3-Methyl-6-(1-methylethyl)-1-cyclohexen-1-yl)acetat 

Relevant academic research and scientific papers

Thermally induced cyclobutenone rearrangements and domino reactions

(Chemical Equation Presented) Four thermal-rearrangement pathways and a domino reaction leading to quinones arise from the thermolysis of cyclobutenones. The course of vinylcyclobutenone rearrangements is dictated by the nature of the substituent, R (see

Kinetic resolution of racemic 2-substituted cyclohexanones by enantioselective deprotonation

Incomplete deprotonation of racemic 2-substituted cyclohexanones (dl-4) by chiral lithium amides (2) in the presence of trimethylsilyl chloride was found to give the corresponding trimethylsilyl enol ethers (5) and the unreacted ketones (4) in reasonably high enantiomeric excesses.