877149-62-7Relevant articles and documents
Isoindolone formation via intramolecular Diels-Alder reaction
Ball, Matthew,Boyd, Alistair,Churchill, Gwydion,Cuthbert, Murray,Drew, Mark,Fielding, Mark,Ford, Gair,Frodsham, Lianne,Golden, Michael,Leslie, Kevin,Lyons, Sarah,McKeever-Abbas, Ben,Stark, Andrew,Tomlin, Paula,Gottschling, Stephen,Hajar, Abraham,Jiang, Ji-Long,Lo, Josephine,Suchozak, Bob
, p. 741 - 747 (2012/07/31)
The intramolecular Diels-Alder reaction provides a useful synthetic methodology to build biologically active and synthetically useful isoindolone ring systems. An application of this methodology, providing an efficient manufacturing route to an mGluR2 positive allosteric modulator via a 1,5,7-substituted isoindolone, is reported herein.
ISOINDOLONE COMPOUNDS AND THEIR USE AS METABOTROPIC GLUTAMATE RECEPTOR POTENTIATORS
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Page/Page column 81, (2008/06/13)
The present invention is directed to compounds of formula (I), wherein R1 is a ring and n is a number from 1 to 8. The invention also relates to use of the compounds in therapy as metabotropic glutamate receptor modulators, particularly in neurological and psychiatric disorders.