Matthew D. Wodrich
Citata da
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Systematic errors in computed alkane energies using B3LYP and other popular DFT functionals
MD Wodrich, C Corminboeuf, PR Schleyer
Organic letters 8 (17), 3631-3634, 2006
How accurate are DFT treatments of organic energies?
MD Wodrich, C Corminboeuf, PR Schreiner, AA Fokin, PR Schleyer
Organic letters 9 (10), 1851-1854, 2007
The concept of protobranching and its many paradigm shifting implications for energy evaluations
MD Wodrich, CS Wannere, Y Mo, PD Jarowski, KN Houk, PR Schleyer
Chemistry–A European Journal 13 (27), 7731-7744, 2007
Bimetallic oxidative addition involving radical intermediates in nickel-catalyzed alkyl–alkyl Kumada coupling reactions
J Breitenfeld, J Ruiz, MD Wodrich, X Hu
Journal of the American Chemical Society 135 (32), 12004-12012, 2013
Evidence for d orbital aromaticity in square planar coinage metal clusters
CS Wannere, C Corminboeuf, ZX Wang, MD Wodrich, RB King, ...
Journal of the American Chemical Society 127 (15), 5701-5705, 2005
Principles of electron capture and transfer dissociation mass spectrometry applied to peptide and protein structure analysis
KO Zhurov, L Fornelli, MD Wodrich, A Laskay, YO Tsybin
Chemical Society Reviews 42 (12), 5014-5030, 2013
Fast and highly chemoselective alkynylation of thiols with hypervalent iodine reagents enabled through a low energy barrier concerted mechanism
R Frei, MD Wodrich, DP Hari, PA Borin, C Chauvier, J Waser
Journal of the American Chemical Society 136 (47), 16563-16573, 2014
How large is the conjugative stabilization of diynes?
PD Jarowski, MD Wodrich, CS Wannere, PR Schleyer, KN Houk
Journal of the American Chemical Society 126 (46), 15036-15037, 2004
Covalent Capture of Nitrous Oxide by N‐Heterocyclic Carbenes
AG Tskhovrebov, E Solari, MD Wodrich, R Scopelliti, K Severin
Angewandte Chemie International Edition 51 (1), 232-234, 2012
Quantification of “fuzzy” chemical concepts: a computational perspective
JF Gonthier, SN Steinmann, MD Wodrich, C Corminboeuf
Chemical Society Reviews 41 (13), 4671-4687, 2012
Room temperature decarboxylative cyanation of carboxylic acids using photoredox catalysis and cyanobenziodoxolones: a divergent mechanism compared to alkynylation
F Le Vaillant, MD Wodrich, J Waser
Chemical science 8 (3), 1790-1800, 2017
Ligand‐Controlled Regiodivergent Pathways of Rhodium (III)‐Catalyzed Dihydroisoquinolone Synthesis: Experimental and Computational Studies of Different Cyclopentadienyl Ligands
MD Wodrich, B Ye, JF Gonthier, C Corminboeuf, N Cramer
Chemistry–A European Journal 20 (47), 15409-15418, 2014
General and Practical Formation of Thiocyanates from Thiols
R Frei, T Courant, MD Wodrich, J Waser
Chemistry-A European Journal 21 (6), 2662-2668, 2015
Bimetallic oxidative addition in nickel-catalyzed alkyl–aryl kumada coupling reactions
J Breitenfeld, MD Wodrich, X Hu
Organometallics 33 (20), 5708-5715, 2014
Empirical corrections to density functional theory highlight the importance of nonbonded intramolecular interactions in alkanes
MD Wodrich, DF Jana, PR Schleyer, C Corminboeuf
The Journal of Physical Chemistry A 112 (45), 11495-11500, 2008
Reconstitution of [Fe]-hydrogenase using model complexes
S Shima, D Chen, T Xu, MD Wodrich, T Fujishiro, KM Schultz, J Kahnt, ...
Nature chemistry 7 (12), 995, 2015
Overcoming systematic DFT errors for hydrocarbon reaction energies
SN Steinmann, MD Wodrich, C Corminboeuf
Theoretical Chemistry Accounts 127 (5-6), 429-442, 2010
Double aromaticity in monocyclic carbon, boron, and borocarbon rings based on magnetic criteria
MD Wodrich, C Corminboeuf, SS Park, PR Schleyer
Chemistry–A European Journal 13 (16), 4582-4593, 2007
Linear scaling relationships and volcano plots in homogeneous catalysis–revisiting the Suzuki reaction
M Busch, MD Wodrich, C Corminboeuf
Chemical science 6 (12), 6754-6761, 2015
Sequential N–O and N–N bond cleavage of N-heterocyclic carbene-activated nitrous oxide with a vanadium complex
AG Tskhovrebov, E Solari, MD Wodrich, R Scopelliti, K Severin
Journal of the American Chemical Society 134 (3), 1471-1473, 2012
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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