Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/99176
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dc.contributor.authorChen, Keen
dc.contributor.authorPullarkat, Sumod A.en
dc.date.accessioned2013-10-31T07:44:01Zen
dc.date.accessioned2019-12-06T20:04:08Z-
dc.date.available2013-10-31T07:44:01Zen
dc.date.available2019-12-06T20:04:08Z-
dc.date.copyright2012en
dc.date.issued2012en
dc.identifier.citationChen, K., & Pullarkat, S. A. (2012). A tandem Heck–aza-Michael addition protocol for the one-pot synthesis of isoindolines from unprotected amines. Organic & biomolecular chemistry, 10(32), 6600-6606.en
dc.identifier.urihttps://hdl.handle.net/10356/99176-
dc.identifier.urihttp://hdl.handle.net/10220/17155en
dc.description.abstractA palladacycle-catalyzed tandem Heck-intramolecular aza-Michael reaction protocol has been developed for the one-pot synthesis of 1-substituted isoindolines from N-unprotected 2-bromobenzylamines and acrylates with high yields.en
dc.language.isoenen
dc.relation.ispartofseriesOrganic & biomolecular chemistryen
dc.subjectDRNTU::Science::Chemistry::Organic chemistryen
dc.titleA tandem Heck–aza-Michael addition protocol for the one-pot synthesis of isoindolines from unprotected aminesen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.identifier.doi10.1039/c2ob25854den
item.fulltextNo Fulltext-
item.grantfulltextnone-
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