Journal
ORGANIC LETTERS
Volume 10, Issue 5, Pages 793-796Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol702922c
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A mild and facile Pd-catalyzed intramolecular chloroamination of unactivated alkenes has been described. This reaction takes place at room temperature and is tolerant of synthetically useful acid-sensitive functional groups. Generally high exo-selectivities are observed in the formation of a variety of 5- and 6-membered rings. This system is unique in its ability to tolerate multidentate ligands on palladium, which opens up the possibility of controlling the absolute sense of induction using a chiral ligand.
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