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dc.contributor.authorRayabarapu, Dinesh Kumar
dc.contributor.authorZhou, Aihua
dc.contributor.authorJeon, Kyu Ok
dc.contributor.authorSamarakoon, Thiwanka Bandara
dc.contributor.authorRolfe, Alan
dc.contributor.authorSiddiqui, Hina
dc.contributor.authorHanson, Paul R.
dc.date.accessioned2017-04-17T20:58:38Z
dc.date.available2017-04-17T20:58:38Z
dc.date.issued2009-04-18
dc.identifier.citationRayabarapu, Dinesh Kumar et al. “α-Haloarylsulfonamides: Multiple Cyclization Pathways to Skeletally Diverse Benzofused Sultams.” Tetrahedron 65.16 (2009): 3180–3188.en_US
dc.identifier.urihttp://hdl.handle.net/1808/23721
dc.description.abstractThe development of new methods to skeletally diverse sultams based on a central α-halo benzene sulfonamide building block is reported. Several salient features of this building block are utilized in multiple reaction pathways, including the Heck reaction, C- and O-arylation, Sonogashira-Pauson-Khand, Sonogashira-intramolecular hydroamination, lithiative cyclization and domino aza-Michael Heck for the generation of 5-, 6- and 7-membered benzofused bicyclic and tricyclic sultams.en_US
dc.publisherElsevieren_US
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 3.0 (CC BY-NC-ND 3.0 US), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/
dc.titleα-Haloarylsulfonamides: Multiple Cyclization Pathways to Skeletally Diverse Benzofused Sultamsen_US
dc.typeArticleen_US
kusw.kuauthorHanson, Paul R.
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.1016/j.tet.2008.11.053en_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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This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 3.0 (CC BY-NC-ND 3.0 US), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
Except where otherwise noted, this item's license is described as: This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 3.0 (CC BY-NC-ND 3.0 US), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.