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dc.contributor.authorMaity, Pradip K.
dc.contributor.authorKainz, Quirin M.
dc.contributor.authorFaisal, Saqib
dc.contributor.authorRolfe, Alan
dc.contributor.authorSamarakoon, Thiwanka Bandara
dc.contributor.authorBasha, Fatima Z.
dc.contributor.authorReiser, Oliver
dc.contributor.authorHanson, Paul R.
dc.date.accessioned2017-02-22T20:50:30Z
dc.date.available2017-02-22T20:50:30Z
dc.date.issued2012-06-14
dc.identifier.citationMaity, Pradip K., Quirin M. Kainz, Saqib Faisal, Alan Rolfe, Thiwanka. B. Samarakoon, Fatima Z. Basha, Oliver Reiser, and Paul R. Hanson. "Intramolecular Monomer-on-monomer (MoM) Mitsunobu Cyclization for the Synthesis of Benzofused Thiadiazepine-dioxides." Chemical Communications 47.46 (2011): 12524.en_US
dc.identifier.urihttp://hdl.handle.net/1808/23222
dc.description.abstractThe utilization of a monomer-on-monomer (MoM) intramolecular Mitsunobu cyclization reaction employing norbornenyl-tagged (Nb-tagged) reagents is reported for the synthesis of benzofused thiadiazepine-dioxides. Facile purification was achieved via ring-opening metathesis (ROM) polymerization initiated by one of three metathesis catalyst methods: (i) free metathesis catalyst, (ii) surface-initiated catalyst-armed silica, or (iii) surface-initiated catalyst-armed Co/C magnetic nanoparticles.en_US
dc.publisherRoyal Society of Chemistryen_US
dc.titleIntramolecular monomer-on-monomer (MoM) mitsunobu cyclization for the synthesis of benzofused thiadiazepine-dioxidesen_US
dc.typeArticleen_US
kusw.kuauthorHanson, Paul R.
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.1039/c1cc14807aen_US
kusw.oaversionScholarly/refereed, author accepted manuscripten_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.rights.accessrightsopenAccess


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