91524-50-4

Upstream product

• 1444-65-1 (RS)-2-phenylcyclohexanone 
• 618-36-0 rac-methylbenzylamine 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 822-87-7 2-Chlorocyclohexanone 
• 2627-86-3 (S)-1-phenyl-ethylamine 

Downstream Products

• 144462-24-8 (2S,6S)-2-(2,2-Bis-benzenesulfonyl-ethyl)-6-phenyl-cyclohexanone 
• 943229-17-2 α-(methylthio)-N-(2-phenylcyclohexen-1-yl)-N-[(R)-1-phenylethyl]acetamide 
• 943229-19-4 2,3,3a,4,5,6-hexahydro-3-methylthio-1-[(R)-1-phenylethyl]-3a-phenylindol-2-one 
• 19988-39-7 (-)-cis-2-Phenyl cyclohexylamine hydrochloride 
• 19988-39-7 (+)-cis-2-Phenyl cyclohexylamine hydrochloride 
• 135972-03-1 (αS,1S,2S)-(-)-cis-2-Phenyl-N-(1-phenylethyl)cyclohexanamin 
• 79315-79-0 ((1R,2R)-2-Phenyl-cyclohexyl)-((R)-1-phenyl-ethyl)-amine; hydrochloride 
• 793624-27-8 (αR,1R,2R)-(-)-cis-2-Phenyl-N-(1-phenylethyl)cyclohexanamin 

Relevant academic research and scientific papers

Stereoselective synthesis of cis and trans-fused 3a-aryloctahydroindoles using cyclization of N-vinylic α-(methylthio)acetamides: synthesis of (-)-mesembrane

Treatment of N-(2-arylcyclohex-1-en-1-yl)-α-(methylthio)acetamides with N-chlorosuccinimide (NCS) gave 3a-aryl-2,3,3a,4,5,6-hexahydro-3-(methylthio)indol-2-ones. Desulfurization of the cyclization products followed by a catalytic hydrogenation of the resu

Asymmetric Michael Addition of Chiral Enaminoesters to Phenyl Vinyl Sulfone and 1,1-bis(Phenylsulfonyl)ethylene

Key words: Asymmetric Michael reactions; chiral enantioesters; phenyl vinyl sulfone; 1,1-bis(phenylsulfonylethylene. Enaminoester (S)-9 was added to phenyl vinyl sulfone, leading to adduct (S)-10.In contrast addition of 9 to 1,1-bis(phenylsulfonyl) ethyle

Asymmetric Reductive Amination of Cycloalkanones, VII: Asymmetric Synthesis of cis-1R,2R- and cis-1S,2S,-2-Arylcyclohexanamines

The asymmetric synthesis of cis-2-arylcyclohexanamines 4 by a three-step procedure is reported: condensation of racemic 2-arylcyclohexanones 1 with the chiral auxiliary R-(+)- or S-(-)-1-phenylethylamine, respectively, leads to a mixture of the imin isomers 2.Upon hydrogenation with Raney-Nickel just one secondary amin of type 3 is obtained, which is hydrogenolyzed to the optically active primary cis-2-arylcyclohexanamines 4.The relative configuration as well as the conformation were derived from 1H-NMR data.The absolute configuration of the highly enantiomericallypure compounds 4 was determined by CD spectra.

Asymmetric Reductive Amination of Cycloalkanones, 2. Synthesis and Absolute Configuration of 2-Substituted Cyclohexanamines

Asymmetric synthesis of 2-substituted cyclohexanamines from racemic cyclohexanones by means of reductive amination in a three-step procedure is described.Condensation of the ketones 5 with the optically active auxiliary amines 6 leads to the imines 7, which are hydrogenated to the secondary amines 8 with Raney nickel.Hydrogenolysis with palladium-on-charcoal yields the primary amines 9.With Raney nickel as catalyst the synthesis of the amines 8 and 9 runs with high chemical yield under complete diastereomeric and high grade enantiomeric control, respectively.Enantiomeric excess is determined via the diastereomeric acylamines 10 by means of HPLC.Stereochemical analysis including the absolute configuration of 8 and 9 is performed with 1H, 13C NMR spectroscopy, via the CD of the salicylidenes 11 and the X-ray spectrum of the amine 9c. - Reaction mechanism is investigated via the partially deuterated amine 13 to come up as a kinetically controlled asymmetric hydrogenation combined with a thermodynamically controlled transformation.

ASYMMETRIC SYNTHESIS OF CIS-2-SUBSTITUTED CYCLOHEXANAMINES WITH HIGHT OPTICAL PURITY

Asymmetric reductive amination of racemic 2-substituted cyclohexanones (R= methyl, ethyl, phenyl, benzyl) using optically active 1-phenyl-ethylamines yields optically active cis-cyclohexanamines.