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 SizeFormat 
open.202000175.pdf16,53 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons