195251-76-4

Upstream product

• 2627-86-3 (S)-1-phenyl-ethylamine 
• 583-60-8 2-Methylcyclohexanone 

Downstream Products

• 79265-63-7 ((1S,2R)-2-Methyl-cyclohexyl)-((S)-1-phenyl-ethyl)-amine; hydrochloride 
• 79265-63-7 ((1S,2R)-2-Methyl-cyclohexyl)-((S)-1-phenyl-ethyl)-amine; hydrochloride 
• 695809-23-5 (αS,1S,2R)-(-)-cis-2-Methyl-N-(1-phenylethyl)cyclohexanamin 
• 53068-89-6 (R)-(+)-2-(2'-carbomethoxyethyl)-2-methylcyclohexanone 
• 10049-61-3 (+)-cis-2-Methyl cyclohexylamine hydrochloride 
• 10049-61-3 (-)-cis-2-Methyl cyclohexylamine hydrochloride 
• 91306-30-8 (R)-(+)-2-methyl-2-(3-oxobutyl)cyclohexanone 
• 2627-86-3 (S)-1-phenyl-ethylamine 
• 63975-59-7 (R)-(-)-4a-methyl-4,4a,5,6,7,8-hexahydro-3H-naphthalene-2-one 
• 33449-59-1 8-Methyl-4,4a,5,6,7,8-hexahydronaphthalen-2(3H)-one 

Relevant academic research and scientific papers

Photochemical Rearrangement of Chiral Oxaziridines in Continuous Flow: Application Toward the Scale-Up of a Chiral Bicyclic Lactam

A method for synthesizing chiral lactams from chiral oxaziridines in continuous flow is described. The oxaziridines are readily available from cyclic ketones. Photolysis of the oxaziridines using the Booker-Milburn flow system provides conversion to the chiral lactams in good yield and short residence times. Application of this chemistry toward the synthesis of a chiral bicyclic lactam is described.

Pyrrolopyrazinyl Urea Kinase Inhibitors

The present invention relates to the use of novel pyrrolopyrazinyl urea derivatives of Formula I, wherein the variables R1, R2, R3, R4, and R5 are defined as described herein, which inhibit JAK and are useful for the treatment of auto-immune and inflammatory diseases.

Asymmetric strecker synthesis of the four α-quaternary 1-amino-2-methylcyclohexanecarboxylic acids

The synthesis of the four 1-amino-2-methylcyclohexanecarboxylic acids 13, 14, 15, and 16 from diastereomeric mixtures of the α-amino nitriles 1-4 by successive application of conc. H2SO4, Pd/C H2, and conc. HCl is describe

Synthesis of Tridensone, a Sesquiterpene Ketone Isolated from the Liverwort Bazzania tridens. Structure Revision and Absolute Configuration

The title compound and its isomer have been synthesized as optically active forms.The spectral data of the natural compounds 1 were identical with those of our synthetic isomer 1a showing that its structure should be revised and its absolute configuration

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.