6560-81-2

Upstream product

• 110-89-4 piperidine 
• 1655-07-8 ethyl 2-oxocyclohexane carboxylate 

Downstream Products

• 292043-65-3 piperidyl-2-oxocyclohex-2-enecarboxamide 
• 1246453-78-0 [9-(2-benzyloxy-ethyl)-2,3,4,9-tetrahydro-1H-carbazol-4-yl]-piperidin-1-yl-methanone 
• 1246453-77-9 2-bromo-6-(piperidine-1-carbonyl)-cyclohexanone 

Relevant academic research and scientific papers

In vivo imaging method for cancer

The present invention provides a method useful in the diagnosis and monitoring of cancer wherein there is an abnormal expression of PBR. The method of the invention is particularly useful in evaluating the severity of the cancer, e.g. PBR expression corre

In vivo imaging method of mood disorders

The present invention provides a method useful in the diagnosis and/or monitoring of mood disorders wherein there is an abnormal expression of PBR. The method of the invention is useful in the differential diagnosis of said mood disorders and other condit

IN VIVO IMAGING METHOD OF MOOD DISORDERS

The present invention provides a method useful in the diagnosis and/or monitoring of mood disorders wherein there is an abnormal expression of PBR. The method of the invention is useful in the differential diagnosis of said mood disorders and other condit

[2 + 2] Photocycloadditions and photorearrangements of 2- alkenylcarboxamido-2-cycloalken-1-ones

While intermolecular photocycloaddition of alkenes with 2- carboxamidocyclo-2-pent-1-enones was not an efficient process, photolysis of 2-alkenylcarboxamido-2-cycloalken-1-ones led regio- and stereospecifically to a faster [2 + 2] intramolecular reaction and therefore to the corresponding cyclobutanes. However, photorearrangements involving three different intramolecular H-abstraction processes, compete with the observed cycloaddition. To explain the results, we propose that different deactivation pathways are available to the excited state, depending on the conformers present in the starting material. (C) 2000 Elsevier Science Ltd.