dc.contributor.author |
O’Broin, Calvin Q. |
dc.contributor.author |
Fernández, Patricia |
dc.contributor.author |
Martínez, Claudio |
dc.contributor.author |
Muñiz, Kilian |
dc.date.accessioned |
2018-01-15T16:04:33Z |
dc.date.accessioned |
2018-02-15T10:27:51Z |
dc.date.available |
2018-01-15T16:04:33Z |
dc.date.available |
2018-02-15T10:27:51Z |
dc.date.issued |
2016 |
dc.identifier.uri |
http://hdl.handle.net/2072/226361 |
dc.identifier.uri |
http://hdl.handle.net/2072/305800 |
dc.language.iso |
eng |
dc.publisher |
ACS publications |
dc.relation |
Ministerio de Economia y Competitivad |
dc.relation |
Cellex ICIQ |
dc.relation |
Fellowship program ICIQ |
dc.relation |
Explora grants to K. M |
dc.relation |
and Severo Ochoa Excellence Accreditation 2014-2018 to ICIQ |
dc.relation |
Photoyodocat (Mineco Explora) |
dc.relation.ispartof |
Organic Letters |
dc.rights |
2016 American Chemical Society |
dc.title |
N-Iodosuccinimide promoted Hofmann-Löffler Reactions of Sulfonimides under Visible Light |
dc.type |
info:eu-repo/semantics/article |
dc.relation.projectID |
CTQ2013-50105-EXP |
dc.relation.projectID |
CTQ2011-25027 |
dc.relation.projectID |
SEV-2013-0319 |
dc.identifier.doi |
https://dx.doi.org/10.1021/acs.orglett.5b03476 |
dc.rights.accessLevel |
info:eu-repo/semantics/openAccess |
dc.description.abstract |
Conditions for an attractive and productive protocol for the position-selective intramolecular C-H amination of aliphatic groups (Hofmann-Löffler reaction) are reported employing sulfonimides as nitrogen sources. N-Iodosuccinimide is the only required promoter for this transformation, which is conveniently initiated by visible light. The overall transformation provides pyrrolidines under mild and selective conditions as demonstrated for 17 different substrates. |