These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. Synthetic and Mechanistic Implications of Chlorine Photoelimination in Nickel/Photoredox C(sp Kariofillis SK; Doyle AG Acc Chem Res; 2021 Feb; 54(4):988-1000. PubMed ID: 33511841 [TBL] [Abstract][Full Text] [Related]
3. Photoredox Mediated Nickel Catalyzed Cross-Coupling of Thiols With Aryl and Heteroaryl Iodides via Thiyl Radicals. Oderinde MS; Frenette M; Robbins DW; Aquila B; Johannes JW J Am Chem Soc; 2016 Feb; 138(6):1760-3. PubMed ID: 26840123 [TBL] [Abstract][Full Text] [Related]
4. General Paradigm in Photoredox Nickel-Catalyzed Cross-Coupling Allows for Light-Free Access to Reactivity. Sun R; Qin Y; Nocera DG Angew Chem Int Ed Engl; 2020 Jun; 59(24):9527-9533. PubMed ID: 32189408 [TBL] [Abstract][Full Text] [Related]
5. Nickel-Catalyzed C-Heteroatom Cross-Coupling Reactions under Mild Conditions via Facilitated Reductive Elimination. Zhu C; Yue H; Jia J; Rueping M Angew Chem Int Ed Engl; 2021 Aug; 60(33):17810-17831. PubMed ID: 33252192 [TBL] [Abstract][Full Text] [Related]
7. Mechanistic Evidence of a Ni(0/II/III) Cycle for Nickel Photoredox Amide Arylation. Bradley RD; McManus BD; Yam JG; Carta V; Bahamonde A Angew Chem Int Ed Engl; 2023 Oct; 62(43):e202310753. PubMed ID: 37684220 [TBL] [Abstract][Full Text] [Related]
8. Highly Chemoselective Iridium Photoredox and Nickel Catalysis for the Cross-Coupling of Primary Aryl Amines with Aryl Halides. Oderinde MS; Jones NH; Juneau A; Frenette M; Aquila B; Tentarelli S; Robbins DW; Johannes JW Angew Chem Int Ed Engl; 2016 Oct; 55(42):13219-13223. PubMed ID: 27436532 [TBL] [Abstract][Full Text] [Related]
9. Elucidation of a Redox-Mediated Reaction Cycle for Nickel-Catalyzed Cross Coupling. Sun R; Qin Y; Ruccolo S; Schnedermann C; Costentin C; Daniel G Nocera J Am Chem Soc; 2019 Jan; 141(1):89-93. PubMed ID: 30563318 [TBL] [Abstract][Full Text] [Related]
10. Investigating the Mechanism of Ni-Catalyzed Coupling of Photoredox-Generated Alkyl Radicals and Aryl Bromides: A Computational Study. Sanosa N; Ruiz-Campos P; Ambrosi D; Sampedro D; Funes-Ardoiz I Int J Mol Sci; 2023 May; 24(11):. PubMed ID: 37298098 [TBL] [Abstract][Full Text] [Related]
11. Halide Noninnocence and Direct Photoreduction of Ni(II) Enables Coupling of Aryl Chlorides in Dual Catalytic, Carbon-Heteroatom Bond-Forming Reactions. Chrisman CH; Kudisch M; Puffer KO; Stewart TK; Lamb YML; Lim CH; Escobar R; Thordarson P; Johannes JW; Miyake GM J Am Chem Soc; 2023 Jun; 145(22):12293-12304. PubMed ID: 37204458 [TBL] [Abstract][Full Text] [Related]
12. Photocatalytic Activation of Less Reactive Bonds and Their Functionalization via Hydrogen-Evolution Cross-Couplings. Chen B; Wu LZ; Tung CH Acc Chem Res; 2018 Oct; 51(10):2512-2523. PubMed ID: 30280898 [TBL] [Abstract][Full Text] [Related]
13. Indole Nucleophile Triggers Mechanistic Divergence in Ni-Photoredox N-Arylation. Liang KJ; Taylor OR; López AL; Woo RJ; Bahamonde A Chemistry; 2024 Jul; ():e202402524. PubMed ID: 39060220 [TBL] [Abstract][Full Text] [Related]
14. Using Data Science To Guide Aryl Bromide Substrate Scope Analysis in a Ni/Photoredox-Catalyzed Cross-Coupling with Acetals as Alcohol-Derived Radical Sources. Kariofillis SK; Jiang S; Żurański AM; Gandhi SS; Martinez Alvarado JI; Doyle AG J Am Chem Soc; 2022 Jan; 144(2):1045-1055. PubMed ID: 34985904 [TBL] [Abstract][Full Text] [Related]