Change search
ReferencesLink to record
Permanent link

Direct link
Palladium- and Nickel-Catalyzed Alkenylation of Enolates
Stockholm University, Faculty of Science, Department of Organic Chemistry.
Stockholm University, Faculty of Science, Department of Organic Chemistry.
2013 (English)In: Chemistry - A European Journal, ISSN 0947-6539, E-ISSN 1521-3765, Vol. 19, no 6, 1858-1871 p.Article, review/survey (Refereed) Published
Abstract [en]

Transition-metal-catalyzed alkenylation of enolates provides a direct method to synthesize broadly useful ,-unsaturated carbonyl compounds from the corresponding carbonyl compound and alkenyl halides. Despite being reported in the early seventies, this reaction class saw little development for many years. In the past decade, however, efforts to develop this reaction further have increased considerably, and many research groups have reported efficient coupling protocols, including enantioselective versions. These reactions most commonly employ palladium catalysts, but there are also some important reports using nickel. There are many examples of this powerful transformation being used in the synthesis of complex natural products.

Place, publisher, year, edition, pages
2013. Vol. 19, no 6, 1858-1871 p.
Keyword [en]
catalysis, CC coupling, enantioselectivity, enolates, natural products, nickel, palladium
National Category
Chemical Sciences
URN: urn:nbn:se:su:diva-88268DOI: 10.1002/chem.201202798ISI: 000314217100001OAI: diva2:610815
Swedish Research Council


Available from: 2013-03-13 Created: 2013-03-12 Last updated: 2013-03-13Bibliographically approved

Open Access in DiVA

No full text

Other links

Publisher's full text
By organisation
Department of Organic Chemistry
In the same journal
Chemistry - A European Journal
Chemical Sciences

Search outside of DiVA

GoogleGoogle Scholar
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

Altmetric score

Total: 36 hits
ReferencesLink to record
Permanent link

Direct link