Z-selective ring-closing metathesis reactions
US-9073801-B2 · Jul 7, 2015 · US
US9586981B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9586981-B2 |
| Application number | US-201314649725-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 12, 2013 |
| Priority date | Dec 12, 2012 |
| Publication date | Mar 7, 2017 |
| Grant date | Mar 7, 2017 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A novel chelated ruthenium-based metathesis catalyst bearing an N-2,6-diisopropylphenyl group is reported and displays near-perfect selectivity for the Z-olefin (>95%), as well as unparalleled TONs of up to 7,400, in a variety of homodimerization and industrially relevant metathesis reactions. This derivative and other new catalytically-active species were synthesized using an improved method employing sodium carboxylates to induce the salt metathesis and C—H activation of these chelated complexes. All of these new ruthenium-based catalysts are highly Z-selective in the homodimerization of terminal olefins.
Opening claim text (preview).
What is claimed is: 1. A process for preparing a macrocyclic compound comprising reacting a C—H activated metathesis catalyst represented by formula 9 with a diene, wherein the diene is represented by the formula 18a and the macrocyclic compound is represented by the formula 18 2. A process for preparing a macrocyclic compound comprising reacting a C—H activated metathesis catalyst represented by formula 9 with a diene, wherein the diene is represented by the formula 19a and the macrocyclic compound is represented by the formula 19 3. A process for preparing a macrocyclic compound comprising reacting a C—H activated metathesis catalyst represented by formula 9 with a diene, wherein the diene is represented by the formula 20a and the macrocyclic compound is represented by the formula 20
Heterocyclic compounds containing rings of more than six members having one oxygen atom as the only ring hetero atom · CPC title
Carbenes or carbynes, i.e.(image) · CPC title
Metal-hydrocarbon complexes · CPC title
Olefin oligomerisation or telomerisation · CPC title
Ruthenium · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.