作者:Matthew Ball、Alistair Boyd、Gwydion Churchill、Murray Cuthbert、Mark Drew、Mark Fielding、Gair Ford、Lianne Frodsham、Michael Golden、Kevin Leslie、Sarah Lyons、Ben McKeever-Abbas、Andrew Stark、Paula Tomlin、Stephen Gottschling、Abraham Hajar、Ji-long Jiang、Josephine Lo、Bob Suchozak
DOI:10.1021/op300002f
日期:2012.5.18
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.
分子内的狄尔斯-阿尔德反应提供了一种有用的合成方法,可以建立具有生物活性和合成意义的异吲哚酮环系统。本文报道了该方法的应用,其通过1,5,7-取代的异吲哚酮提供了向mGluR2阳性变构调节剂的有效制造途径。