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Mendeleev Communications, 2022, Volume 32, Issue 5, Pages 619–621
DOI: https://doi.org/10.1016/j.mencom.2022.09.016
(Mi mendc744)
 

This article is cited in 3 scientific papers (total in 3 papers)

Communications

Highly enantioselective amination of η3-(2-fluorocycloheptenyl)palladium complexes bearing chiral P,P- and P,N-ligands

A. Yu. Bobrovaa, M. A. Novikova, R. A. Novikova, P. V. Dorovatovskiib, A. D. Volodinc, A. A. Korlyukovc, Yu. V. Tomilova

a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b National Research Centre 'Kurchatov Institute', Moscow, Russian Federation
c A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (410 kB) Citations (3)
Abstract: The key enantioselectivity-determining step in Pd-catalyzed asymmetric amination of 2-fluoroallylic substrates was optimized using model reaction of η3-(2-fluorocycloheptenyl)-palladium complexes bearing chiral P,P- and P,N-ligands with various amines. (S)-ButPHOX was found to be the most effective ligand allowing the formation of 2-fluoroallyl amines and anilines with high enantioselectivity.
Keywords: fluoroalkenes, 2-fluoroallyl amines, enantioselective catalysis, chiral palladium complexes, allylic amination.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.7 Mb)


Citation: A. Yu. Bobrova, M. A. Novikov, R. A. Novikov, P. V. Dorovatovskii, A. D. Volodin, A. A. Korlyukov, Yu. V. Tomilov, “Highly enantioselective amination of η3-(2-fluorocycloheptenyl)palladium complexes bearing chiral P,P- and P,N-ligands”, Mendeleev Commun., 32:5 (2022), 619–621
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  • This publication is cited in the following 3 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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