70144-20-6

Upstream product

• 14679-29-9 (+/-)-1-methyl-cyclohex-4-ene-1r,2c-dicarboxylic acid-2-methyl ester 
• 357418-52-1 cis-(1S,2R)-(-)-1-methyl-1,2,3,6-tetrahydrophthalic anhydride 
• 31915-48-7 (+/-)-1-methyl-cyclohex-4-ene-1r,2c-dicarboxylic acid 
• 67-56-1 methanol 
• 25357-31-7 1-methyl-cis-4-cyclohexene-1,2-dicarboxylic anhydride 

Downstream Products

• 14679-45-9 cis-1,2-Dihydroxymethyl-1-methyl-4-cyclohexen 
• 70090-48-1 (1R,6S)-6-Methyl-6-((S)-1-phenyl-ethylcarbamoyl)-cyclohex-3-enecarboxylic acid methyl ester 
• 70090-48-1 (1S,6R)-6-Methyl-6-((S)-1-phenyl-ethylcarbamoyl)-cyclohex-3-enecarboxylic acid methyl ester 
• 61214-26-4 Methanesulfonic acid (1S,6R)-6-methanesulfonyloxymethyl-1-methyl-cyclohex-3-enylmethyl ester 

Relevant academic research and scientific papers

Bond Fixation in Annulenes. 8. Assessment of the Ring Inversion and Bond Shifting Barriers in 1,2,3-trimethylcyclooctatetraene. Resolution, Absolute Configuration and Circular Dichroism Behavior of an Annulene Hydrocarbon

A synthesis of racemic 1,2,3-trimethylcyclooctatetraene (13) based upon the expectation that 1,7,8-trimethylbicycloocta-2,4,7-triene (12) would open disrotatorily under orbital symmetry control was realized.This annulene demonstrated a ready pro