Please use this identifier to cite or link to this item:
doi:10.22028/D291-33182
Title: | The Allylic Alkylation of Ketone Enolates |
Author(s): | Junk, Lukas Kazmaier, Uli |
Language: | English |
Title: | ChemistryOpen |
Volume: | 9 |
Issue: | 9 |
Pages: | 929-952 |
Publisher/Platform: | Wiley |
Year of Publication: | 2020 |
Free key words: | allylic alkylations enolates ketones palladium transition metals |
DDC notations: | 500 Science 540 Chemistry |
Publikation type: | Journal Article |
Abstract: | The palladium-catalyzed allylic alkylation of non-stabilized ketone enolates was thought for a long time to be not as efficient as the analogous reactions of stabilized enolates, e. g. of malonates and β-ketoesters. The field has experienced a rapid development during the last two decades, with a range of new, highly efficient protocols evolved. In this review, the early developments as well as current methods and applications of palladium-catalyzed ketone enolate allylations will be discussed. |
DOI of the first publication: | 10.1002/open.202000175 |
Link to this record: | urn:nbn:de:bsz:291--ds-331821 hdl:20.500.11880/30519 http://dx.doi.org/10.22028/D291-33182 |
ISSN: | 2191-1363 |
Date of registration: | 1-Feb-2021 |
Faculty: | NT - Naturwissenschaftlich- Technische Fakultät |
Department: | NT - Chemie |
Professorship: | NT - Prof. Dr. Uli Kazmaier |
Collections: | SciDok - Der Wissenschaftsserver der Universität des Saarlandes |
Files for this record:
File | Description | Size | Format | |
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open.202000175.pdf | 16,53 MB | Adobe PDF | View/Open |
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