58711-32-3

Upstream product

• 58711-07-2 1-ethyl-2-oxocyclohexaneacetic acid 
• 74-88-4 methyl iodide 
• 4423-94-3 2-ethylcyclohexanone 
• 96-32-2 bromoacetic acid methyl ester 
• 3274-96-2 2-ethylcyclohexanol 

Downstream Products

• 103012-99-3 1-ethyl-2-oxocyclohex-3-eneacetic acid methyl ester 
• 115867-83-9 1-ethyl-2-oxo-4(phenylmethyl)cyclohexaneacetic acid methyl ester 
• 112126-57-5 [(1S,4S)-1-Ethyl-4-(2-methyl-allyl)-2-oxo-cyclohexyl]-acetic acid methyl ester 
• 112126-57-5 [(1S,4R)-1-Ethyl-4-(2-methyl-allyl)-2-oxo-cyclohexyl]-acetic acid methyl ester 
• 106464-30-6 ((1S,4S)-4-Allyl-1-ethyl-2-oxo-cyclohexyl)-acetic acid methyl ester 
• 106464-30-6 ((1S,4R)-4-Allyl-1-ethyl-2-oxo-cyclohexyl)-acetic acid methyl ester 

Relevant academic research and scientific papers

Substituted 2-oxocyclohexaneacetic acid esters

Process for the production of substituted 2-oxocyclohexaneacetic acid esters and intermediates used for their production. The substituted 2-oxocyclohexaneacetic acid esters are themselves useful intermediates for the manufacture of substituted 2,3,4,9-tet

1,4-DIASTEREOSELECTIVITY IN THE ADDITION OF ALLYLSTANNANES TO 1-ALKYL-2-OXOCYCLOHEX-3-ENEACETIC ACID METHYL ESTERS

Cyclohexanones 1 were allowed to react with allyltrimethylsilane and three allyltributylstannanes in the presence of titanium tetrachloride.Products 2 and 3 were formed in ratios ranging from 7:1 to 26:1 (2:3).Ratios resulting from the use of other Lewis acids support 4 as an intermediate which accounts for the observed stereoselectivity.

Process for preparing substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives and methods for their preparation and use are disclosed. The compounds are useful analgesic and antiinflammatory agents.

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives and methods for their preparation and use are disclosed. The compounds are useful analgesic and antiinflammatory agents.

Production of substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives and methods for their preparation. The compounds are useful analgesic and anti-inflammatory agents.

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid, compositions and use

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives and methods for their preparation and use are disclosed. The compounds are useful analgesic and antiinflammatory agents.

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives, compositions and use

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives and methods for their preparation and use are disclosed. The compounds are useful analgesic and antiinflammatory agents.

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid, compositions and use

Substituted 2,3,4,9-tetrahydro-1H-carbazole-1-acetic acid derivatives and methods for their preparation and use are disclosed. The compounds are useful analgesic and antiinflammatory agents.

Carbazole acetic acid derivatives

Tetrahydrocyclopent[b]indole-3-acetic acid, tetrahydrocarbazole-1-acetic acid and hexahydrocyclohept[b]-indole-6-acetic acid derivatives in which the carbon bearing alkyl, lower alkenyl or lower cycloalkyl are disclosed. The compounds are useful antiinflammatory agents and methods for their preparation and use are described.

Cycloalkanoindoles. I. Synthesis and antiinflammatory actions of some acidic tetrahydrocarbazoles, cyclopentindoles, and cycloheptindoles

A novel series of acidic cycloalkanoindoles comprising tetrahydrocarbazole, cyclopentindole, and cycloheptindole 1 acetic acids has been synthesized via the Fischer indolization between a phenylhydrazine and a 1 alkyl 2 oxocycloalkaneacetic acid ester. Th