39891-70-8Relevant academic research and scientific papers
The discovery and SAR of indoline-3-carboxamides - A new series of 5-HT6 antagonists
Reid, Mark,Carlyle, Ian,Caulfield, Wilson L.,Clarkson, Tom R.,Cusick, Fiona,Epemolu, Ola,Gilfillan, Robert,Goodwin, Richard,Jaap, David,O'Donnell, Elise C.,Presland, Jeremy,Rankovic, Zoran,Spinks, Daniel,Spinks, Gayle,Thomson, Anne M.,Thomson, Fiona,Strain, James,Wishart, Grant
scheme or table, p. 3713 - 3716 (2010/09/04)
Antagonists of the 5-HT6 receptor have been shown to improve cognitive function in a wide range of animal models and as such may prove to be attractive agents for the symptomatic treatment of cognitive disorders such as Alzheimer's disease (AD) and schizophrenia. We report herein the identification and SAR around N-(2-aminoalkyl)-1-(arylsulfonyl)indoline-3-carboxamides - a novel chemotype of 5-HT6 antagonists.
Stereoselective synthesis of optically active cyclic α- And β-amino esters through lipase-catalyzed transesterification or interesterification processes
Alatorre-Santamaria, Sergio,Gotor-Fernandez, Vicente,Gotor, Vicente
experimental part, p. 2307 - 2313 (2010/11/05)
A series of cyclic α- and β-amino esters belonging to a family of indolines and quinolines have been efficiently synthesized to study their behavior in lipase-mediated kinetic resolution reactions. The influence of the fused ring structure to the benzene ring and the position of the ester functionality relative to the amino group have been demonstrated, finding excellent values of enantiodiscrimination in the transesterification reaction of methyl indoline-3-carboxylate with n-butanol catalyzed by Candida antarctica lipase B being observed. On the other hand, low to moderate selectivities have been found when using a wide panel of lipases toward methyl indoline-2- carboxylate or 1,2,3,4-tetrahydroquinoline derivatives in alkoxycarbonylation, transesterification or interesterification reactions.
