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54James P. Blinco, Kathryn E. Fairfull-Smith, Aaron S. Micallef and Steven E. Bottle*.
Highly efficient, stoichiometric radical exchange reactions using isoindoline profluorescent nitroxides, Polym. Chem., 2010, 1, 1009. Chao Wang, Xiao-Hua Chen, Shi-Ming Zhou and Liu-Zhu Gong.
Asymmetric organocatalytic formal double-arylation of azomethines for the synthesis of highly enantiomerically enriched isoindolines, Chem. Commun., 2010, 46, 1275. Kristen Nicole Clary, Masood Parvez and Thomas George Back.
Preparation of 1-aryl-substituted isoindoline derivatives by sequential Morita–Baylis–Hillman and intramolecular Diels–Alder reactions, Org. Biomol. Chem., 2009, 7, 1226. Paweł DydioPresent address: Van't Hoff Institute for Molecular Sciences, University of Amsterdam, Science Park 904, 1098 XH, Amsterdam, The Netherlands., Dawid Lichosyt and Janusz Jurczak.
Amide- and urea-functionalized pyrroles and benzopyrroles as synthetic, neutral anion receptors, Chem. Soc. Rev., 2011, 40, 2971. David Heckman, Mohamed I. Attia, Mira A. M. Behnam, Amal M. Y. Mohsen, Christian Markl, Justin Julius, Shalini Sethi, Paula A. Witt-Enderby and Darius P. Zlotos.
2-[(1,3-Dihydro-2H-isoindol-2-yl)methyl]melatonin – a novel MT-selective melatonin receptor antagonist, Med. Chem. Commun., 2011, 2, 991. Ke Chen and Sumod A. Pullarkat.
A tandem Heck–aza-Michael addition protocol for the one-pot synthesis of isoindolines from unprotected amines, Org. Biomol. Chem., 2012, 10, 6600. Daniel L. Priebbenow, Scott G. Stewart and Frederick M. Pfeffer.
A general approach to N-heterocyclic scaffolds using domino Heck–aza-Michael reactions, Org. Biomol. Chem., 2011, 9, 1508. Fan et al..
Unexpected E-stereoselective reductive A3-coupling reaction of terminal alkynes with aldehydes and amines, Nature Communications, 2014 A Novel Reaction of Tetracyanoethylene with N-Aryl-Isoindolines, Organic Free Radicals