130913-07-4

Upstream product

• 130913-06-3 (1R,4R)-5-Hydroxy-5-phenyl-bicyclo[2.2.2]octan-2-one 
• 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 
• 130913-04-1 C₁₀H₁₄O₃ 
• 130913-05-2 C₁₆H₂₀O₃ 
• 76478-52-9 (1S,4S)-(-)-bicyclo<2.2.2>oct-7-ene-2,5-dione 
• 1131282-53-5 (1R,4R,5S,6S)-6-hydroxy-5-phenylbicyclo[2.2.2]octan-2-one 
• 1351983-75-9 (1R,2S,3S,4R)-6-oxo-3-phenylbicyclo[2.2.2]octan-2-yl methanesulfonate 
• 930-68-7 cyclohexenone 
• 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 
• 130913-06-3 5-hydroxy-5-phenylbicyclo<2.2.2>octan-2-one 

Downstream Products

• 1374793-36-8 (1R,4R)-5-phenylbicyclo[2.2.2]octa-2,5-dien-2-yl trifluoromethanesulfonate 
• 1374793-25-5 (1R,4R)-2-phenyl-5-(o-tolyl)bicyclo[2.2.2]octa-2,5-diene 
• 1374793-16-4 C₂₁H₂₂O 
• 1374793-32-4 (1R,4R)-2-(naphthalen-2-yl)-5-phenylbicyclo[2.2.2]octa-2,5-diene 
• 1374793-23-3 C₂₄H₂₂O 
• 1374793-30-2 (1R,4R)-2-([1,1'-biphenyl]-4-yl)-5-phenylbicyclo[2.2.2]octa-2,5-diene 
• 1374793-21-1 C₂₆H₂₄O 
• 1374793-28-8 (1R,4R)-2-(4-phenoxyphenyl)-5-phenylbicyclo[2.2.2]octa-2,5-diene 
• 1374793-19-7 C₂₆H₂₄O₂ 
• 1374793-29-9 2-((1R,4R)-5-phenylbicyclo[2.2.2]octa-2,5-dien-2-yl)thiophene 
• 1374793-37-9 (1R,4R)-2-methyl-5-phenylbicyclo[2.2.2]octa-2,5-diene 
• 1374793-38-0 (1R,4R)-2-benzyl-5-phenylbicyclo[2.2.2]octa-2,5-diene 
• 1374793-39-1 (1R,4R)-2-isobutyl-5-phenylbicyclo[2.2.2]octa-2,5-diene 
• 1374793-33-5 (1R,4R)-2-(3,5-difluorophenyl)-5-phenylbicyclo[2.2.2]octa-2,5-diene 

Relevant academic research and scientific papers

PREPARATION OF BICYCLO[2.2.2]OCTAN-2-ONE COMPOUNDS

The present invention relates to a new process for the preparation of 6-hydroxy-5-arylbicyclo[2.2.2]octan-2-one compounds of the formula (II); which may subsequently be further transformed to compounds of the formula (I): The present invention further relates to novel compounds as such, which compounds are useful intermediates in the above process.

PREPARATION OF BICYCLO[2.2.2]OCTAN-2-ONE COMPOUNDS

The present invention relates to a new process for the preparation of 6-hydroxy-5-arylbicyclo[2.2.2]octan-2-one compounds of the formula (II); which may subsequently be further transformed to compounds of the formula (I): The present invention further relates to novel compounds as such, which compounds are useful intermediates in the above process.

Scalable synthesis of enantiomerically pure bicyclo[2.2.2]octadiene ligands

An operationally simple and scalable synthesis of enantiomerically pure bicyclo[2.2.2]octadiene (bod) ligands relying on an organocatalytic one-pot Michael addition-aldol reaction with cheap 2-cyclohexenone and phenylacetaldehyde is presented. The crystalline bicyclic product 4a (6-hydroxy-5-phenylbicyclo[2.2.2]octan-2-one) is transformed into phenylbicyclo[2.2.2]oct-5-en-2-one 2, a versatile starting material for the 2-step synthesis of both symmetrical, such as Hayashi's Ph-bod* ligand, as well as novel unsymmetrical chiral dienes.

Design and scale-up of a practical enantioselective route to 5-Phenylbicyclo[2.2.2]oct-5-en-2-one

A practical enantioselective route to chiral 5-phenylbicyclo[2.2.2]oct-5- en-2-one 1 has been designed and developed. The target compound has been obtained as colorless crystals in 22% yield from 2-cyclohexenone, with an enantiomeric ratio higher than 99.5:0.5 and notably high chemical purity (> 99%). Three intermediates out of nine chemical steps are isolated. It is noteworthy that this process is devoid of any chromatography or distillation although all but one intermediate are oils. Key to success was the optimization of an intramolecular aldol reaction of an in situ prepared ketone aldehyde leading to the solid intermediate (1R,4R,4S,6S)-6-hydroxybicyclo[2.2.2]octan-2- one 9a that is isolated in very high chemical and chiral purity. This is an example of an intramolecular crystallization-induced diastereomer transformation (CIDT). The dehydration of this secondary alcohol to 1 required an extensive screen of reaction conditions to secure an excellent purity, essential for crystallization of this low-melting compound. The final process is simple and concentrated as demonstrated by an expeditious synthesis of 1 kg of 1 in a 30-L reactor in 10 working days.

DIASTEREOSELECTIVE PREPARATION OF BICYCLO[2.2.2]OCTAN-2-ONE COMPOUNDS

The present invention relates to a new process for the diastereoselective preparation of (1R*,4R*,5S*,6S*)-6-hydroxy-5-arylbicyclo[2.2.2]octan-2-one compounds, the compounds of the formula (II), which may subsequently be further transformed to 5-aryl-bicy

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