Halogenations of Aryl Substituted Sydnones

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Halogenations of Aryl Substituted Sydnones

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dc.contributor Turnbull, Kenneth
dc.contributor Benson, Jennifer
dc.contributor Clark, Ashley
dc.contributor Liddy, Kyle
dc.contributor Morehead, Jeffrey
dc.contributor Oxman, Kyle
dc.contributor.author Brown, Daniel
dc.date.accessioned 2012-05-21T15:06:36Z
dc.date.available 2012-05-21T15:06:36Z
dc.date.created 2012-04-13
dc.date.issued 2012-04-13
dc.identifier.other celebration_abstract12_brown_d
dc.identifier.uri http://hdl.handle.net/2374.WSU/6028
dc.description.abstract

Recently, a novel avenue to the iodination of sydnones at the 4-position has been developed using N-iodosuccinimide in acetic acid (cf. 1 to 2). The scope of this concept will be enumerated using various activated and deactivated arylsydnones, and extended by means of other halogenating reagents, such as N- chlorosuccinimide and N-bromosuccinimide.

dc.language.iso en_US en_US
dc.publisher Wright State University en_US
dc.relation.ispartof Celebration of Research, Scholarship, and Creative Activities en_US
dc.rights.uri http://www.wright.edu/web/copyright.html
dc.subject Brown, Daniel en_US
dc.subject Turnbull, Kenneth en_US
dc.subject Benson, Jennifer en_US
dc.subject Clark, Ashley en_US
dc.subject Liddy, Kyle en_US
dc.subject Morehead, Jeffrey en_US
dc.subject Oxman, Kyle en_US
dc.subject Wright State University. College of Science and Mathematics. Department of Chemistry en_US
dc.title Halogenations of Aryl Substituted Sydnones en_US
dc.type Presentation en_US
dc.permissions World
dc.publisher.digital Digital Services Department, Wright State University Libraries en_US
dc.date.digitized 2012-04-13
dc.publisher.OLinstitution Wright State University en_US

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