Most Cited Publications

Papers with >100 citations

(Updated 11 Jan 2022)

H-index = 47.

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] [1272 Citations]
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] [350 Citations]
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] [320 Citations]
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] [315 Citations]
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] [281 Citations]
Fahmi Himo, Per E.M. Siegbahn,
Quantum Chemical Studies of Radical-Containing Enzymes,
Chem. Rev. 2003, 103, 2421-2456.
[link] [233 Citations]
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] [229 Citations]
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] [190 Citations]
Fahmi Himo,
Quantum Chemical Modeling of Enzyme Active Sites and Reaction Mechanisms,
Theor. Chem. Acc. 2006, 116, 232-240.
[link] [169 Citations]
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] [169 Citations]
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] [156 Citations]
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] [141 Citations]
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] [140 Citations]
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] [135 Citations]
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] [125 Citations]
Fahmi Himo, Astrid Gräslund, Leif A. Eriksson,
Density Functional Calculations on Model Tyrosyl Radicals,
Biophys. J. 1997, 72, 1556-1567.
[link] [116 Citations]
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] [110 Citations]
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] [101 Citations]