130913-06-3

Upstream product

• 130913-05-2 C₁₆H₂₀O₃ 
• 130913-04-1 C₁₀H₁₄O₃ 
• 76478-52-9 (1S,4S)-(-)-bicyclo<2.2.2>oct-7-ene-2,5-dione 
• 1192365-33-5 5-(ethylenedioxy)-2-phenylbicyclo<2.2.2>octan-2-ol 
• 132435-30-4 5-(ethylenedioxy)bicyclo<2.2.2>octan-2-one 
• 57346-05-1 Bicyclo<2.2.2>octane-2,4-dione 
• 17660-74-1 bicyclo[2.2.2]oct-7-ene-2,5-dione 
• 76478-53-0 1R,4S-(-)-bicyclo<2.2.2>octane-2,5-dione 

Downstream Products

• 132486-17-0 (1R,4R)-5-phenylbicyclo[2.2.2]oct-5-en-2-one 
• 130913-09-6 (R)-2-Phenyl-bicyclo[2.2.2]octane 
• 130913-08-5 (1R,4R,5S)-5-Phenyl-bicyclo[2.2.2]octan-2-one 
• 130913-08-5 (1R,4R,5R)-5-Phenyl-bicyclo[2.2.2]octan-2-one 
• 130913-07-4 2-phenylbicyclo<2.2.2>oct-2-en-5-one 
• 130913-08-5 endo-5-phenylbicyclo<2.2.2>octan-2-one 
• 130913-08-5 exo-5-phenylbicyclo<2.2.2>octan-2-one 
• 132267-83-5 endo-2-phenyl<5,5,6,6-²H4>bicyclo<2.2.2>octane 

Relevant academic research and scientific papers

Stereomutation of 7-Tropylionorbornane, 2-Tropyliobicyclooctane, and 2-Tropylioadamantane: Evidence for the Intermediacy of Heptafulvenes

The perchlorates of 7-tropylionorbornane (3), 2-tropyliobicyclooctane (4), and 2-tropylioadamantane (5) were found to undergo stereomutation in acetonitrile at 25-85 deg C, as evidenced by following the change in the 13C NMR spectra of their deuter

SYNTHESES AND RACEMIZATION VIA INTERMOLECULAR PROTOTROPY OF OPTICALLY ACTIVE ALKYLTROPYLIUM IONS. A NOVEL SCALE FOR THE KINETIC BROENSTED BASICITY OF ORGANIC SOLVENTS

Optically active (1-methylpropyl)tropylium ion (1) and (2-bicyclooctyl)tropylium ion (2) have been synthesized.The first-order rate constants of racemization via intermolecular prototropy of 1 provide a novel scale for the kinetic Broensted basicit