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Redox-Neutral Cross-Coupling Amination with Weak N- Nucleop..:

Chen Zhu (445894) ; Ajit Prabhakar Kale (1643506) ; Huifeng Yue (1461376).
https://figshare.com/articles/journal_contribution/Redox-Neutral_Cross-Coupling_Amination_with_Weak_i_N-_i_Nucleophiles_Arylation_of_Anilines_Sulfonamides_Sulfoximines_Carbamates_and_Imines_via_Nickelaelectrocatalysis/14788118. , 2021

Link: https://doi.org/10.1021/jacsau.1c00148.s001

RT Journal
T1 <Title>Redox-Neutral Cross-Coupling Amination with Weak N- Nucleophiles: Arylation of Anilines, Sulfonamides, Sulfoximines, Carbamates, and Imines via Nickelaelectrocatalysis</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_14788118&Exemplar=1&LAN=DE
				
A1 Chen Zhu (445894)
A1 Ajit Prabhakar Kale (1643506)
A1 Huifeng Yue (1461376)
A1 Magnus Rueping (1489489)
YR 2021
K1 Biophysics
K1 Biochemistry
K1 Molecular Biology
K1 Pharmacology
K1 Ecology
K1 Immunology
K1 Environmental Sciences not elsewhere classified
K1 Biological Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 Physical Sciences not elsewhere classified
K1 electron-deficient anilines
K1 reductive elimination pathway
K1 benzophenone imine
K1 sulfonamide
K1 nickel-catalyzed cross-coupling ami
K1 Weak N
K1 nitrogen nucleophiles
K1 product selectivity
K1 Aryl halides
K1 Redox-Neutral Cross-Coupling Amination
K1 base switch
K1 imine product
K1 DFT calculations support
K1 aryl tosylates
JF https://figshare.com/articles/journal_contribution/Redox-Neutral_Cross-Coupling_Amination_with_Weak_i_N-_i_Nucleophiles_Arylation_of_Anilines_Sulfonamides_Sulfoximines_Carbamates_and_Imines_via_Nickelaelectrocatalysis/14788118
LK http://dx.doi.org/https://doi.org/10.1021/jacsau.1c00148.s001
DO https://doi.org/10.1021/jacsau.1c00148.s001
SF ELIB - SuUB Bremen

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