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1 Ergebnisse
1
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
Redox-Neutral Cross-Coupling Amination with Weak N- Nucleophiles: Arylation of Anilines, Sulfonamides, Sulfoximines, Carbamates, and Imines via Nickelaelectrocatalysis
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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