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. Catalytic Nitrene Homocoupling by an Iron(II) Bis(alkoxide) Complex: Bulking Up the Alkoxide Enables a Wider Range of Substrates and Provides Insight into the Reaction Mechanism. Yousif M; Wannipurage D; Huizenga CD; Washnock-Schmid E; Peraino NJ; Ozarowski A; Stoian SA; Lord RL; Groysman S Inorg Chem; 2018 Aug; 57(15):9425-9438. PubMed ID: 30015481 [TBL] [Abstract][Full Text] [Related]
3. Catalytic N-N coupling of aryl azides to yield azoarenes via trigonal bipyramid iron-nitrene intermediates. Mankad NP; Müller P; Peters JC J Am Chem Soc; 2010 Mar; 132(12):4083-5. PubMed ID: 20199026 [TBL] [Abstract][Full Text] [Related]
4. Deciphering Iron-Catalyzed C-H Amination with Organic Azides: N Stroek W; Keilwerth M; Malaspina LA; Grabowsky S; Meyer K; Albrecht M Chemistry; 2024 Jan; 30(4):e202303410. PubMed ID: 37916523 [TBL] [Abstract][Full Text] [Related]
5. Road Map for the Construction of High-Valued Roy S; Das SK; Khatua H; Das S; Chattopadhyay B Acc Chem Res; 2021 Dec; 54(23):4395-4409. PubMed ID: 34761918 [TBL] [Abstract][Full Text] [Related]
6. Navigating the Unnatural Reaction Space: Directed Evolution of Heme Proteins for Selective Carbene and Nitrene Transfer. Yang Y; Arnold FH Acc Chem Res; 2021 Mar; 54(5):1209-1225. PubMed ID: 33491448 [TBL] [Abstract][Full Text] [Related]
7. Nitrene Radical Intermediates in Catalytic Synthesis. Kuijpers PF; van der Vlugt JI; Schneider S; de Bruin B Chemistry; 2017 Oct; 23(56):13819-13829. PubMed ID: 28675476 [TBL] [Abstract][Full Text] [Related]
8. Isoelectronic Manganese and Iron Hydrogenation/Dehydrogenation Catalysts: Similarities and Divergences. Gorgas N; Kirchner K Acc Chem Res; 2018 Jun; 51(6):1558-1569. PubMed ID: 29863334 [TBL] [Abstract][Full Text] [Related]
9. Bioinspired Manganese and Iron Complexes for Enantioselective Oxidation Reactions: Ligand Design, Catalytic Activity, and Beyond. Sun W; Sun Q Acc Chem Res; 2019 Aug; 52(8):2370-2381. PubMed ID: 31333021 [TBL] [Abstract][Full Text] [Related]
10. Recent progress in asymmetric bifunctional catalysis using multimetallic systems. Shibasaki M; Kanai M; Matsunaga S; Kumagai N Acc Chem Res; 2009 Aug; 42(8):1117-27. PubMed ID: 19435320 [TBL] [Abstract][Full Text] [Related]
11. Exploration of earth-abundant transition metals (Fe, Co, and Ni) as catalysts in unreactive chemical bond activations. Su B; Cao ZC; Shi ZJ Acc Chem Res; 2015 Mar; 48(3):886-96. PubMed ID: 25679917 [TBL] [Abstract][Full Text] [Related]
12. Mechanism of cobalt(II) porphyrin-catalyzed C-H amination with organic azides: radical nature and H-atom abstraction ability of the key cobalt(III)-nitrene intermediates. Lyaskovskyy V; Suarez AI; Lu H; Jiang H; Zhang XP; de Bruin B J Am Chem Soc; 2011 Aug; 133(31):12264-73. PubMed ID: 21711027 [TBL] [Abstract][Full Text] [Related]
13. Beyond the Second Coordination Sphere: Engineering Dirhodium Artificial Metalloenzymes To Enable Protein Control of Transition Metal Catalysis. Lewis JC Acc Chem Res; 2019 Mar; 52(3):576-584. PubMed ID: 30830755 [TBL] [Abstract][Full Text] [Related]
14. Highly selective biaryl cross-coupling reactions between aryl halides and aryl Grignard reagents: a new catalyst combination of N-heterocyclic carbenes and iron, cobalt, and nickel fluorides. Hatakeyama T; Hashimoto S; Ishizuka K; Nakamura M J Am Chem Soc; 2009 Aug; 131(33):11949-63. PubMed ID: 19639999 [TBL] [Abstract][Full Text] [Related]
15. Iron- and Cobalt-Catalyzed Alkene Hydrogenation: Catalysis with Both Redox-Active and Strong Field Ligands. Chirik PJ Acc Chem Res; 2015 Jun; 48(6):1687-95. PubMed ID: 26042837 [TBL] [Abstract][Full Text] [Related]
17. Interplay between Theory and Experiment for Ammonia Synthesis Catalyzed by Transition Metal Complexes. Tanaka H; Nishibayashi Y; Yoshizawa K Acc Chem Res; 2016 May; 49(5):987-95. PubMed ID: 27105472 [TBL] [Abstract][Full Text] [Related]
18. Transition-metal-catalyzed C-N bond forming reactions using organic azides as the nitrogen source: a journey for the mild and versatile C-H amination. Shin K; Kim H; Chang S Acc Chem Res; 2015 Apr; 48(4):1040-52. PubMed ID: 25821998 [TBL] [Abstract][Full Text] [Related]