Most Cited Publications
Papers with >100 citations (Web of Science)
(Updated 6 Aug 2024)
H-index = 52 (Web of Science), 61 (GoogleScholar).
1.
Fahmi Himo, Timothy Lovell, Robert Hilgraf, Vsevolod V. Rostovtsev, Louis Noodleman, K. Barry Sharpless, Valery V. Fokin,
Copper(I)-Catalyzed Synthesis of Azoles. DFT Study Predicts Unprecedented Reactivity and Intermediates,
J. Am. Chem. Soc. 2005, 127, 210-216.
[link] [1473 Citations]
Copper(I)-Catalyzed Synthesis of Azoles. DFT Study Predicts Unprecedented Reactivity and Intermediates,
J. Am. Chem. Soc. 2005, 127, 210-216.
[link] [1473 Citations]
2.
Margareta R.A. Blomberg, Tomasz Borowski, Fahmi Himo, Rong-Zhen Liao, Per E.M. Siegbahn,
Quantum Chemical Studies of Mechanisms for Metalloenzymes,
Chem. Rev. 2014, 114, 3601-3658.
[link] [469 Citations]
Quantum Chemical Studies of Mechanisms for Metalloenzymes,
Chem. Rev. 2014, 114, 3601-3658.
[link] [469 Citations]
3.
Fahmi Himo, Zachary P. Demko, Louis Noodleman, K. Barry Sharpless,
Why is Tetrazole Formation by Addition of Azide to Organic Nitriles Catalyzed by Zn(II) Salts?,
J. Am. Chem. Soc. 2003, 125, 9983-9987.
[link] [348 Citations]
Why is Tetrazole Formation by Addition of Azide to Organic Nitriles Catalyzed by Zn(II) Salts?,
J. Am. Chem. Soc. 2003, 125, 9983-9987.
[link] [348 Citations]
4.
Louis Noodleman, Timothy Lovell, Wen-Ge Han, Jian Li, Fahmi Himo,
Quantum Chemical Studies of Intermediates and Reaction Pathways in Selected Enzymes and Catalytic Synthetic Systems,
Chem. Rev. 2004, 104, 459-508.
[link] [326 Citations]
Quantum Chemical Studies of Intermediates and Reaction Pathways in Selected Enzymes and Catalytic Synthetic Systems,
Chem. Rev. 2004, 104, 459-508.
[link] [326 Citations]
5.
Fahmi Himo, Zachary P. Demko, Louis Noodleman, K. Barry Sharpless,
Mechanisms of Tetrazole Formation by Addition of Azide to Nitriles,
J. Am. Chem. Soc. 2002, 124, 12210-12216.
[link] [312 Citations]
Mechanisms of Tetrazole Formation by Addition of Azide to Nitriles,
J. Am. Chem. Soc. 2002, 124, 12210-12216.
[link] [312 Citations]
6.
Per E.M. Siegbahn, Fahmi Himo,
The Quantum Chemical Cluster Approach for Modeling Enzyme Reactions,
Wiley Interdisciplinary Reviews, Comput. Mol. Sci. 2011, 1, 323-336.
[link] [250 Citations]
The Quantum Chemical Cluster Approach for Modeling Enzyme Reactions,
Wiley Interdisciplinary Reviews, Comput. Mol. Sci. 2011, 1, 323-336.
[link] [250 Citations]
7.
Per E.M. Siegbahn, Fahmi Himo,
Recent Developments of the Quantum Chemical Cluster Approach for Modeling Enzyme Reactions,
J. Biol. Inorg. Chem. 2009, 14, 643-651.
[link] [248 Citations]
Recent Developments of the Quantum Chemical Cluster Approach for Modeling Enzyme Reactions,
J. Biol. Inorg. Chem. 2009, 14, 643-651.
[link] [248 Citations]
8.
Fahmi Himo, Per E.M. Siegbahn,
Quantum Chemical Studies of Radical-Containing Enzymes,
Chem. Rev. 2003, 103, 2421-2456.
[link] [246 Citations]
Quantum Chemical Studies of Radical-Containing Enzymes,
Chem. Rev. 2003, 103, 2421-2456.
[link] [246 Citations]
9.
Joel Malmgren, Stefano Santoro, Nazli Jalalian, Fahmi Himo, Berit Olofsson,
Arylation with Unsymmetrical Diaryliodonium Salts: a Chemoselectivity Study,
Chem. Eur. J. 2013, 19, 10334-10342.
[link] [207 Citations]
Arylation with Unsymmetrical Diaryliodonium Salts: a Chemoselectivity Study,
Chem. Eur. J. 2013, 19, 10334-10342.
[link] [207 Citations]
10.
Fahmi Himo,
Recent Trends in Quantum Chemical Modeling of Enzymatic Reactions,
J. Am. Chem. Soc. 2017, 139, 6780–6786.
[[link]] [179 Citations]
Recent Trends in Quantum Chemical Modeling of Enzymatic Reactions,
J. Am. Chem. Soc. 2017, 139, 6780–6786.
[[link]] [179 Citations]
11.
Fahmi Himo,
Quantum Chemical Modeling of Enzyme Active Sites and Reaction Mechanisms,
Theor. Chem. Acc. 2006, 116, 232-240.
[link] [179 Citations]
Quantum Chemical Modeling of Enzyme Active Sites and Reaction Mechanisms,
Theor. Chem. Acc. 2006, 116, 232-240.
[link] [179 Citations]
12.
Armando Cordova, Henrik Sunden, Anders Bogevig, Mikael Johansson, Fahmi Himo,
The Direct Catalytic Asymmetric α-Aminooxylation Reaction: Development of Stereoselective Routes to 1,2-Diols and 1,2-Amino Alcohols and Density Functional Calculations,
Chem. Eur. J. 2004, 10, 3673-3684.
[link] [163 Citations]
The Direct Catalytic Asymmetric α-Aminooxylation Reaction: Development of Stereoselective Routes to 1,2-Diols and 1,2-Amino Alcohols and Density Functional Calculations,
Chem. Eur. J. 2004, 10, 3673-3684.
[link] [163 Citations]
13.
Ismail Ibrahem, Ramon Rios, Jan Vesely, Peter Hammar, Lars Eriksson, Fahmi Himo, Armando Cordova,
Enantioselective Organocatalytic Hydrophosphination of α,β-Unsaturated Aldehydes,
Angew. Chem. Int. Ed. 2007, 46, 4507-4510.
[link] [156 Citations]
Enantioselective Organocatalytic Hydrophosphination of α,β-Unsaturated Aldehydes,
Angew. Chem. Int. Ed. 2007, 46, 4507-4510.
[link] [156 Citations]
14.
Jeremy N. Harvey, Fahmi Himo, Feliu Maseras, Lionel Perrin,
Scope and Challenge of Computational Methods for Studying Mechanism and Reactivity in Homogeneous Catalysis,
ACS Catal. 2019, 9, 6803-6813.
[link] [148 Citations]
Scope and Challenge of Computational Methods for Studying Mechanism and Reactivity in Homogeneous Catalysis,
ACS Catal. 2019, 9, 6803-6813.
[link] [148 Citations]
15.
Tommaso Marcelli, Peter Hammar, Fahmi Himo,
Phosphoric Acid-Catalyzed Enantioselective Transfer Hydrogenation of Imines: a Density Functional Theory Study of the Reaction Mechanism and Origins of Stereoselectivity,
Chem. Eur. J. 2008, 14, 8562-8571.
[link] [148 Citations]
Phosphoric Acid-Catalyzed Enantioselective Transfer Hydrogenation of Imines: a Density Functional Theory Study of the Reaction Mechanism and Origins of Stereoselectivity,
Chem. Eur. J. 2008, 14, 8562-8571.
[link] [148 Citations]
16.
Per E.M. Siegbahn, Leif Eriksson, Fahmi Himo, Maria Pavlov,
Hydrogen Atom Transfer in Ribonucleotide Reductase (RNR),
J. Phys. Chem. B 1998, 102, 10622-10629.
[link] [141 Citations]
Hydrogen Atom Transfer in Ribonucleotide Reductase (RNR),
J. Phys. Chem. B 1998, 102, 10622-10629.
[link] [141 Citations]
17.
Arianna Bassan, Weibiao Zou, Efraim Reyes, Fahmi Himo, Armando Cordova,
The Origin of Stereoselectivity in Primary Amino Acid Catalyzed Intermolecular Aldol Reactions,
Angew. Chem. Int. Ed. 2005, 44, 7028-7032.
[link] [131 Citations]
The Origin of Stereoselectivity in Primary Amino Acid Catalyzed Intermolecular Aldol Reactions,
Angew. Chem. Int. Ed. 2005, 44, 7028-7032.
[link] [131 Citations]
18.
Fahmi Himo, Leif A. Eriksson, Feliu Maseras, Per E.M. Siegbahn,
Catalytic Mechanism of Galactose Oxidase: A Theoretical Study,
J. Am. Chem. Soc. 2000, 122, 8031-8036.
[link] [119 Citations]
Catalytic Mechanism of Galactose Oxidase: A Theoretical Study,
J. Am. Chem. Soc. 2000, 122, 8031-8036.
[link] [119 Citations]
19.
Fahmi Himo, Astrid Gräslund, Leif A. Eriksson,
Density Functional Calculations on Model Tyrosyl Radicals,
Biophys. J. 1997, 72, 1556-1567.
[link] [116 Citations]
Density Functional Calculations on Model Tyrosyl Radicals,
Biophys. J. 1997, 72, 1556-1567.
[link] [116 Citations]
20.
Ismail Ibrahem, Stefano Santoro, Fahmi Himo, Armando Cordova,
Enantioselective Conjugate Silyl Additions to α,β-Unsaturated Aldehydes Catalyzed by Combination of Transition Metal and Chiral Amine Catalysts,
Adv. Synth. Catal. 2011, 353, 245-252.
[link] [112 Citations]
Enantioselective Conjugate Silyl Additions to α,β-Unsaturated Aldehydes Catalyzed by Combination of Transition Metal and Chiral Amine Catalysts,
Adv. Synth. Catal. 2011, 353, 245-252.
[link] [112 Citations]
21.
Louis Noodleman, Timothy Lovell, Tiqing Liu, Fahmi Himo, Rhonda Torres,
Insights into Properties and Energetics of Iron-Sulfur Proteins from Simple Clusters to Nitrogenase,
Current Opinion in Chemical Biology 2002, 6, 259-273.
[link] [112 Citations]
Insights into Properties and Energetics of Iron-Sulfur Proteins from Simple Clusters to Nitrogenase,
Current Opinion in Chemical Biology 2002, 6, 259-273.
[link] [112 Citations]
22.
Ana Popović-Bijelić, Christian R. Kowol, Maria E.S. Lind, Jinghui Luo, Fahmi Himo, Éva A. Enyedy, Vladimir B. Arion, Astrid Gräslund,
Ribonucleotide Reductase Inhibition by Metal Complexes of Triapine (3-Aminopyridine-2-Carboxaldehyde Thiosemicarbazone): A Combined Experimental and Theoretical Study,
J. Inorg. Biochem. 2011, 105, 1422-1431.
[link] [104 Citations]
Ribonucleotide Reductase Inhibition by Metal Complexes of Triapine (3-Aminopyridine-2-Carboxaldehyde Thiosemicarbazone): A Combined Experimental and Theoretical Study,
J. Inorg. Biochem. 2011, 105, 1422-1431.
[link] [104 Citations]
