Andrew Whiting andy.whiting@durham.ac.uk
Emeritus Professor
Andrew Whiting andy.whiting@durham.ac.uk
Emeritus Professor
Katrina S. Madden
Sylvain David
Jonathan P. Knowles
Vinyliodide reacts chemoselectively under Heck-Mizoroki conditions with terminal alkenes, including vinylboronate esters, to give dienes. The resulting dienylboronates undergo Suzuki-Miyaura coupling with aryl, heteroaryl and alkenyl halides to access dienes and trienes.
Whiting, A., Madden, K. S., David, S., & Knowles, J. P. (2015). Heck-Mizoroki Coupling of Vinyliodide and Applications in The Synthesis of Dienes and Trienes. Chemical Communications, 51(57), 11409-11412. https://doi.org/10.1039/c5cc03273c
Journal Article Type | Article |
---|---|
Acceptance Date | Jun 10, 2015 |
Publication Date | Jul 21, 2015 |
Deposit Date | Jun 11, 2015 |
Publicly Available Date | Jun 10, 2016 |
Journal | Chemical Communications |
Print ISSN | 1359-7345 |
Electronic ISSN | 1364-548X |
Publisher | Royal Society of Chemistry |
Peer Reviewed | Peer Reviewed |
Volume | 51 |
Issue | 57 |
Pages | 11409-11412 |
DOI | https://doi.org/10.1039/c5cc03273c |
Public URL | https://durham-repository.worktribe.com/output/1406630 |
Accepted Journal Article
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