Model for the exceptional reactivity of peroxiredoxins 2 and 3 with hydrogen peroxide: a kinetic and computational studyGas-Phase Non-Identity S N 2 Reactions of Halide Anions with Methyl Halides: A High-Level Computational StudyObituary: John A. Pople (1925-2004).Accurate quantum chemical energies for tetrapeptide conformations: why MP2 data with an insufficient basis set should be handled with caution.Factors Controlling the Addition of Carbon-Centered Radicals to Alkenes-An Experimental and Theoretical Perspective.Computational design of effective, bioinspired HOCl antioxidants: the role of intramolecular Cl+ and H+ shifts.In search of radical intermediates in the reactions catalyzed by lysine 2,3-aminomutase and lysine 5,6-aminomutase.Ab initio investigation of the fragmentation of 5,5-diamino-substituted 1,4,2-oxathiazoles.H and D attachment to naphthalene: spectra and thermochemistry of cold gas-phase 1-C10H9 and 1-C10H8D radicals and cations.Hydrogen-atom attack on phenol and toluene is ortho-directed.Hydrogen-adduction to open-shell graphene fragments: spectroscopy, thermochemistry and astrochemistry.Reactivity of disulfide bonds is markedly affected by structure and environment: implications for protein modification and stability.Modeling the reactions catalyzed by coenzyme B12-dependent enzymes.Thermochemistry and kinetics of hydrogen abstraction by methyl radical from polycyclic aromatic hydrocarbons.α-Hydrogen Abstraction by •OH and •SH Radicals from Amino Acids and Their Peptide Derivatives.W3X: A Cost-Effective Post-CCSD(T) Composite Procedure.Evaluation of the heats of formation of corannulene and C60 by means of high-level theoretical procedures.Understanding the mechanism of action of B12-dependent ethanolamine ammonia-lyase: synergistic interactions at play.Ab initio evidence for slow fragmentation in RAFT polymerization.Design of radical-resistant amino acid residues: a combined theoretical and experimental investigation.Base-catalyzed hydrogenation: rationalizing the effects of catalyst and substrate structures and solvation.Chemoselective peptide ligation-desulfurization at aspartate.One-electron reduction of N-chlorinated and N-brominated species is a source of radicals and bromine atom formation.The carbon-skeleton rearrangement in tropane alkaloid biosynthesis.Divergent mechanisms of suicide inactivation for ethanolamine ammonia-lyase.Hydrogen-atom abstraction from a model amino acid: dependence on the attacking radical.Bond dissociation energies and radical stabilization energies: an assessment of contemporary theoretical procedures.On the inclusion of post-MP2 contributions to double-hybrid density functionals.Watson-Crick Base Pair Radical Cation as a Model for Oxidative Damage in DNA.Effect of Hydrogen Bonding and Partial Deprotonation on the Oxidation of Peptides.Impact of Hydrogen Bonding on the Susceptibility of Peptides to Oxidation.Performance of Gradient-Corrected and Hybrid Density Functional Theory: Role of the Underlying Local Density Approximation and the Gradient Correction.An assessment of theoretical procedures for predicting the thermochemistry and kinetics of hydrogen abstraction by methyl radical from benzene.Assessment of theoretical procedures for calculating barrier heights for a diverse set of water-catalyzed proton-transfer reactions.Restricted-Open-Shell G4(MP2)-Type Procedures.Role of Hydrogen Bonding on the Reactivity of Thiyl Radicals: A Mass Spectrometric and Computational Study Using the Distonic Radical Ion Approach.BDE261: a comprehensive set of high-level theoretical bond dissociation enthalpies.David Parker Craig AO FAA. 23 December 1919—1 July 2015Understanding the Mechanism of B12-Dependent Methylmalonyl-CoA Mutase: Partial Proton Transfer in ActionToward a Low-Barrier Transition-Metal-Free Catalysis of Hydrogenation Reactions: A Theoretical Mechanistic Study of HAlX4-Catalyzed Hydrogenations of Ethene (X = F, Cl, and Br)
P50
Q28115866-F9991779-EA48-4418-A52E-59F8BC9EDC77Q29037217-0ADDAB5A-4840-413C-8C37-C4B09DD3D192Q30341337-C80BA56A-2034-4E92-BCE6-FE92BCC3E88AQ30588373-110DEFBE-B10D-47E9-9E4E-B307D0AD7A32Q34228661-E6F12FEC-3CC6-4A6A-A7A5-F0DAC0369217Q34311445-F56FA953-093C-4A8C-9EA5-EDA06558B417Q34590518-76ED0A43-D3A8-4C88-9C7D-A4A9F260A509Q34952533-A5FA8DFD-B542-4CF2-AD33-86BC3652C04DQ35574580-D36EA295-0CF6-4DDC-B65B-7367DB99D0E7Q35947355-A9B7E943-95F7-4410-9FD5-76D591DF2ECCQ36357314-F1F50E19-DD9D-4929-883C-0D688312D8B9Q37493551-6A9F26AE-B53C-4F9C-9B63-4A334D4FF9F3Q37688015-1F98C5A6-C73B-4CFB-8AED-EA50CE239F7CQ39342273-37071EE6-8676-447E-A5B6-D1985A61ACABQ39942861-CEF7754F-0066-452B-8CBF-F7ECC7C4979CQ40304727-8F65B958-3F0B-47E5-B8C7-88E5FAFED1F3Q43438488-12ED6523-FD99-4D70-8915-F5AD8D833CD0Q44222105-149E5D89-F52B-4DE0-A80C-832ED843C567Q44303368-C68FF2F4-CBCA-4B43-AA0B-A43F9D79A5EDQ44386752-6463AD47-3509-414D-9231-E426C2B72276Q45277961-B20F7F04-01C9-4E00-B5D2-87B538AFEB11Q45892251-118D92A5-7486-458D-8A94-87D05D44C066Q46071287-919C0489-6E2D-4803-8AB8-58CE5D0BB848Q46483871-7DF4817E-9F34-4582-9756-AFFA9C612AF9Q46545396-9842190E-5638-46B7-9B8F-0314E2B8C61FQ46859681-E55EBB76-43AB-4513-8F31-8B69508E6545Q46875469-9160E975-9490-4294-A249-7C89BE5F0FFEQ47566472-97A75857-B6C1-4E85-A171-3787892B63FBQ48006394-D8C9D89C-EDA5-45EF-9312-1462459E1772Q48042153-4CEF0ECD-8B8E-4F10-9E13-BC3864E00009Q48093721-36D2B9DD-02FA-466B-A3D2-7A7D3FADE747Q49038047-97B71A82-BF30-4388-B58C-27F41FC443F5Q49079696-76601AA3-81AD-4F80-9169-186AEC472CCCQ49161387-0CE299F4-CFBA-42E4-91EE-303C9ACE7308Q51083234-F5F23FDC-88B4-4892-B441-343AFC052E32Q51140680-F45F569D-E5A7-4B45-80A2-714982B35F72Q51602361-1D70B65D-A3D1-4437-AC20-CD12085E120FQ55882133-51D027C0-2435-4667-9FF7-9188CF306B92Q56566686-604CA5B1-1BE3-47AC-8801-35205A3D751BQ56975999-F63F99E9-6823-4F25-BA4E-3D68C4B84606
P50
description
Austraalia keemik
@et
Australian chemist
@en
Australian chemist
@en-ca
Australian chemist
@en-gb
australischer Chemiker
@de
aŭstralia kemiisto
@eo
chimist australian
@ro
chimiste australien
@fr
cimiciste australian
@lfn
kiemavan Laustralänik
@vo
name
Leo Radom
@ast
Leo Radom
@de
Leo Radom
@en
Leo Radom
@es
Leo Radom
@fr
Leo Radom
@nl
Leo Radom
@sl
type
label
Leo Radom
@ast
Leo Radom
@de
Leo Radom
@en
Leo Radom
@es
Leo Radom
@fr
Leo Radom
@nl
Leo Radom
@sl
prefLabel
Leo Radom
@ast
Leo Radom
@de
Leo Radom
@en
Leo Radom
@es
Leo Radom
@fr
Leo Radom
@nl
Leo Radom
@sl
P166
P214
P269
P106
P1412
P166
P19
P21
P213
0000 0004 0812 3320
P214
P2381
P269
P31
P496
0000-0001-8249-1314
P569
1944-12-13T00:00:00Z
P734
P735
P7859
viaf-300632416