Metal controlled regioselectivity in the cyclometallation of 2-(1-naphthyl)-pyridine.
Författare
Summary, in English
Cyclometallation of 2-(1-naphthyl)-pyridine is described. While cyclopalladation results in a five-membered metallacycle, cycloauration displays a completely orthogonal regioselectivity, resulting in the six-membered ring analogue. Bromination of the gold metallacycle results in the new C-H functionalisation product 2-(8-bromonaphth-1-yl)pyridine.
Publiceringsår
2015
Språk
Engelska
Sidor
911-913
Publikation/Tidskrift/Serie
Chemical Communications
Volym
51
Issue
5
Dokumenttyp
Artikel i tidskrift
Förlag
Royal Society of Chemistry
Ämne
- Chemical Sciences
Status
Published
ISBN/ISSN/Övrigt
- ISSN: 1364-548X