Browse by author
Lookup NU author(s): Dr Matt HopkinsonORCiD
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
Due to the strong potential of C-H activation in many areas of organic chemistry, the use of a pre-existing carbonyl group for the installation of a directing group to enable selective and predictable α-alkenylation with activated olefins as coupling partners is described. This Heck-type reaction would then lead either to β,γ-unsaturated ketones or to variously substituted 1,4-butadienes depending on the conditions used for the cleavage of the directing group. © 2014 American Chemical Society.
Author(s): Boultadakis-Arapinis M, Hopkinson MN, Glorius F
Publication type: Article
Publication status: Published
Journal: Organic Letters
Year: 2014
Volume: 16
Issue: 6
Pages: 1630-1633
Print publication date: 21/03/2014
Online publication date: 03/03/2014
Acceptance date: 23/01/2014
ISSN (print): 1523-7060
ISSN (electronic): 1523-7052
Publisher: American Chemical Society
URL: https://doi.org/10.1021/ol500258q
DOI: 10.1021/ol500258q
PubMed id: 24588566
Altmetrics provided by Altmetric