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dc.contributor.authorSamarakoon, Thiwanka Bandara
dc.contributor.authorLoh, Joanna K.
dc.contributor.authorRolfe, Alan
dc.contributor.authorLe, Lisa S.
dc.contributor.authorYoon, Sun Young
dc.contributor.authorLushington, Gerald H.
dc.contributor.authorHanson, Paul R.
dc.date.accessioned2017-03-28T15:43:30Z
dc.date.available2017-03-28T15:43:30Z
dc.date.issued2011-10-07
dc.identifier.citationSamarakoon, T. B., Loh, J. K., Rolfe, A., Le, L. S., Yoon, S. Y., Lushington, G. H., & Hanson, P. R. (2011). Reaction Pairing: A Diversity-Oriented Synthesis Strategy for the Synthesis of Diverse Benzofused Sultams. Organic Letters, 13(19), 5148–5151. http://doi.org/10.1021/ol201962nen_US
dc.identifier.urihttp://hdl.handle.net/1808/23497
dc.description.abstractA reaction pairing strategy centered on utilization of a reaction triad (sulfonylation, SNAr addition and Mitsunobu alkylation) generating skeletally diverse benzofused tricyclic and bicyclic sultams is reported. Pairing sulfonylation and SNAr reactions yields bridged, tricyclic and bicyclic benzofused sultams. Application of the Mitsunobu reaction in a sulfonylation–Mitsunobu–SNAr pairing allows access to benzo-oxathiazocine-1,1-dioxides, while a simple change in the order of pairing to sulfonylation–SNAr–Mitsunobu affords structurally different, benzofused bridged tricyclic sultams.en_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://dx.doi.org/10.1021/ol201962n.en_US
dc.titleReaction Pairing: A Diversity-Oriented Synthesis Strategy for the Synthesis of Diverse Benzofused Sultamsen_US
dc.typeArticleen_US
kusw.kuauthorSamarkoon, Thiwanka Bandara
kusw.kuauthorLoh, Joanna K.
kusw.kuauthorRolfe, Alan
kusw.kuauthorLe, Lisa S.
kusw.kuauthorYoon, Young Sun
kusw.kuauthorLushington, Gerald H.
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.1021/ol201962nen_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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