Show simple item record

dc.contributor.authorHenderson, Anna R. P.
dc.contributor.authorKosowan, Joel R.
dc.contributor.authorWood, Tabitha E.
dc.date.accessioned2020-03-04T22:14:14Z
dc.date.available2020-03-04T22:14:14Z
dc.date.issued2017-01-16
dc.identifier.citationHenderson, Anna R. P., Joel R. Kosowan, and Tabitha E. Wood, "The Truce-Smiles rearrangement and related reactions: a review." Canadian Journal of Chemistry 95(5) (2017): 483-504. DOI: 10.1139/cjc-2016-0594.en_US
dc.identifier.issn0008-4042
dc.identifier.urihttp://hdl.handle.net/10680/1777
dc.descriptionpost-printen_US
dc.description.abstractThe Truce–Smiles rearrangement is an X → C aryl migration reaction that is achieved by an intramolecular nucleophilic aromatic substitution pathway. The reaction exhibits a wide substrate scope with respect to a migrating aryl ring and leaving group, appearing in many different tandem reaction sequences, to achieve a wide variety of product outcomes. We present an extensive survey of reported examples of the Truce–Smiles rearrangement from the chemistry literature (1950s until present) organized by various substrate design variables or aspects of the reaction method. Present deficiencies in our understanding of the reaction are identified with recommendations for future research directions and useful developments in the application of the reaction are celebrated.en_US
dc.description.urihttps://www.nrcresearchpress.com/doi/full/10.1139/cjc-2016-0594#.XmAlnKhKgdMen_US
dc.language.isoenen_US
dc.publisherNRC Research Pressen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectOrganic chemistryen_US
dc.subjectNamed organic reactionsen_US
dc.subjectRearrangement reactionen_US
dc.subjectAryl migration reactionen_US
dc.subjectReaction methodologyen_US
dc.titleThe Truce–Smiles rearrangement and related reactions: a reviewen_US
dc.typeArticleen_US
dc.identifier.doi10.1139/cjc-2016-0594en_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record