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Formal [4+3] Epoxide Cascade Reaction via a Complementary Ambiphilic Pairing Strategy
| dc.contributor.author | Rolfe, Alan | |
| dc.contributor.author | Samarakoon, Thiwanka Bandara | |
| dc.contributor.author | Hanson, Paul R. | |
| dc.date.accessioned | 2017-03-23T16:03:51Z | |
| dc.date.available | 2017-03-23T16:03:51Z | |
| dc.date.issued | 2010-03-19 | |
| dc.identifier.citation | Rolfe, A., Samarakoon, T. B., & Hanson, P. R. (2010). Formal [4+3] Epoxide Cascade Reaction via a Complementary Ambiphilic Pairing Strategy. Organic Letters, 12(6), 1216–1219. http://doi.org/10.1021/ol100035e | en_US |
| dc.identifier.uri | http://hdl.handle.net/1808/23472 | |
| dc.description.abstract | A formal [4+3] epoxide cascade protocol utilizing ambiphilic sulfonamides and a variety of epoxides (masked ambiphiles) has been developed for the generation of benzothiaoxazepine-1,1′-dioxides and oxathiazepine-1,1′-dioxides. This protocol combines an epoxide ring-opening with either an SNAr or oxa-Michael cyclization pathway. | en_US |
| dc.publisher | American Chemical Society | en_US |
| dc.rights | This 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/ol100035e | en_US |
| dc.title | Formal [4+3] Epoxide Cascade Reaction via a Complementary Ambiphilic Pairing Strategy | en_US |
| dc.type | Article | en_US |
| kusw.kuauthor | Rolfe, Alan | |
| kusw.kuauthor | Samarakoon, Thiwanka Bandara | |
| kusw.kudepartment | Chemistry | en_US |
| dc.identifier.doi | 10.1021/ol100035e | en_US |
| kusw.oaversion | Scholarly/refereed, author accepted manuscript | en_US |
| kusw.oapolicy | This item meets KU Open Access policy criteria. | en_US |
| dc.rights.accessrights | openAccess |
