Please use this identifier to cite or link to this item: doi:10.22028/D291-33244
Title: Stereoselective Allylic Alkylations of Amino Ketones and Their Application in the Synthesis of Highly Functionalized Piperidines
Author(s): Prudel, Cynthia
Huwig, Kai
Kazmaier, Uli
Language: English
Title: Chemistry - A European Journal
Volume: 26
Issue: 14
Pages: 3181-3188
Publisher/Platform: Wiley
Year of Publication: 2020
Free key words: allylic alkylation
chelates
enolates
ketones
palladium
piperidines
DDC notations: 500 Science
540 Chemistry
600 Technology
Publikation type: Journal Article
Abstract: Chelated ketone enolates are excellent nucleophiles for allylic alkylations. Electron-withdrawing groups on the allyl moiety allow subsequent intramolecular Michael additions giving rise to piperidines with up to five stereogenic centers.
DOI of the first publication: 10.1002/chem.202000051
Link to this record: urn:nbn:de:bsz:291--ds-332441
hdl:20.500.11880/30595
http://dx.doi.org/10.22028/D291-33244
ISSN: 1521-3765
0947-6539
Date of registration: 9-Feb-2021
Description of the related object: Supporting Information
Related object: https://chemistry-europe.onlinelibrary.wiley.com/action/downloadSupplement?doi=10.1002%2Fchem.202000051&file=chem202000051-sup-0001-misc_information.pdf
Faculty: NT - Naturwissenschaftlich- Technische Fakultät
Department: NT - Chemie
Professorship: NT - Prof. Dr. Uli Kazmaier
Collections:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

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