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Selective GlyT1 inhibitors: discovery of [4-(3-fluoro-5-trifluoromethylpyridin-2-yl)piperazin-1-yl][5-methanesulfonyl-2-((S)-2,2,2-trifluoro-1-methylethoxy)phenyl]methanone (RG1678), a promising novel medicine to treat schizophrenia.

Alexander Alanine, Markus Bender, Edilio Borroni, 2010, Journal of medicinal chemistry.

Synthesis of 4,6-Dihydro-4-oxopyrido[2,1-a]isoindroles and 4,6-Dihydro-6-oxothieno[2',3',:3,4]pyrrolo[1,2-a]pyridines

U. Widmer, S. Burner, R. Canesso, 1994 .

Discovery of benzoylisoindolines as a novel class of potent, selective and orally active GlyT1 inhibitors.

Markus Bender, Edilio Borroni, Daniela Alberati, 2010, Bioorganic & medicinal chemistry letters.

Radiosynthesis of [5-[ 11C]methanesulfonyl-2-((S)-2,2,2- trifluoro-1-methyl-ethoxy)-phenyl]-[5-(tetrahydro-pyran-4-yl)-1, 3-dihydro-isoindol-2-yl]-methanone ([ 11C]RO5013853), a novel PET tracer for the glycine transporter type i (GlyT1)

Thomas Hartung, Daniel P. Holt, Robert F. Dannals, 2011 .