Iron(III)-catalysed carbonyl–olefin metathesis
Jacob R. Ludwig,
Paul M. Zimmerman,
Joseph B. Gianino and
Corinna S. Schindler ()
Additional contact information
Jacob R. Ludwig: University of Michigan, Willard Henry Dow Laboratory, 930 North University Avenue
Paul M. Zimmerman: University of Michigan, Willard Henry Dow Laboratory, 930 North University Avenue
Joseph B. Gianino: University of Michigan, Willard Henry Dow Laboratory, 930 North University Avenue
Corinna S. Schindler: University of Michigan, Willard Henry Dow Laboratory, 930 North University Avenue
Nature, 2016, vol. 533, issue 7603, 374-379
Abstract:
The olefin metathesis reaction of two unsaturated substrates is one of the most powerful carbon–carbon-bond-forming reactions in organic chemistry; here, a catalytic carbonyl–olefin ring-closing metathesis reaction is demonstrated that uses iron, an abundant and environmentally benign metal, as a catalyst.
Date: 2016
References: Add references at CitEc
Citations:
Downloads: (external link)
https://www.nature.com/articles/nature17432 Abstract (text/html)
Access to the full text of the articles in this series is restricted.
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:nature:v:533:y:2016:i:7603:d:10.1038_nature17432
Ordering information: This journal article can be ordered from
https://www.nature.com/
DOI: 10.1038/nature17432
Access Statistics for this article
Nature is currently edited by Magdalena Skipper
More articles in Nature from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().