sameAs
P184
Nature of O2 and CO binding to metalloporphyrins and heme proteinsSpectroscopy and dynamics of the dipole‐bound state of acetaldehyde enolateModel compounds for the T state of hemoglobinCooperativity in O2 binding to iron porphyrins.Carbon monoxide binding to iron porphyrinsEpoxidation of olefins by cytochrome P-450 model compounds: mechanism of oxygen atom transfer.Geometry dependence of the ring-opening E2 reaction in lactones.Steric and solvation effects in ionic S(N)2 reactions.The RS-.HSR Hydrogen Bond: acidities of alpha,omega-dithiols and electron affinities of their monoradicals.Mechanism of dihydrogen cleavage by high-valent metal oxo compounds: experimental and computational studies.Conformation-dependent reaction thermochemistry: study of lactones and lactone enolates in the gas phase.Dynamics of competitive reactions: endothermic proton transfer and exothermic substitution.Donor ligand effect on the nature of the oxygenating species in Mn(III)(salen)-catalyzed epoxidation of olefins: experimental evidence for multiple active oxidants.Steric retardation of SN2 reactions in the gas phase and solution.Radical autoxidation and autogenous O2 evolution in manganese-porphyrin catalyzed alkane oxidations with chlorite.Hydrogen bonding lowers intrinsic nucleophilicity of solvated nucleophiles.Acidities in cyclohexanediols enhanced by intramolecular hydrogen bonds.Proton exchange and transesterification reactions of acetate enolates with alcohols in the gas phase.Catalytic Activation of H(2) and C-H Bonds by Electron-Deficient Ruthenium(II) Porphyrins.Vinyl hydrogen acidities of two stereoisomers.Fixation of carbon dioxide by carbamyl phosphate synthetase of Escherichia coli. Evidence for a reversibly formed intermediate.Epoxidation of olefins by cytochrome P-450 model compounds: kinetics and stereochemistry of oxygen atom transfer and origin of shape selectivityComputers.CHEMISTRY: Not So SimpleSynthesis and characterization of the "pocket" porphyrinsThe ‘pocket’ porphyrins: Hemoprotein models with lowered CO affinitiesThe "pocket" porphyrin: a hemoprotein model with lowered carbon monoxide affinityModels for the active site of oxygen-binding hemoproteins. Dioxygen binding properties and the structures of (2-methylimidazole)-meso-tetra(.alpha.,.alpha.,.alpha.,.alpha.-o-pivalamidophenyl)porphyrinatoiron(II)-ethanol and its dioxygen adductOxygen binding to cobalt porphyrinsStructural changes upon oxygenation of an iron(II)(porphyrinato)(imidazole) complexOxygen binding to iron porphyrinsReversibility Relationship in Collision-Complex-Forming Bimolecular ReactionsCollisional relaxation of vibrational excitation: Effects of bath gas structureControl of ion kinetic energy in ion cyclotron resonance spectrometry: Very-low-energy collision-induced dissociationLow energy collision induced dissociation: phase-shifting excitation control of ion kinetic energy in ion cyclotron resonance spectrometryTwo-step assay of erythrocyte transketolase activityBioinorganic chemistryComputing in scienceRegioselective and enantioselective epoxidation catalyzed by metalloporphyrinsPhotochemistry. Twist and fluoresce
P50
Q24561640-459FA4EA-ED8A-4825-A923-9A3ABAD19F88Q29042161-6C99837A-7917-4E3E-BB83-9EB30EE3C00FQ33959105-60AFCF84-2CC7-4B25-B575-52968A3A922FQ33964706-AE7FA12B-D7DB-4632-82A4-A0E27A6CBD31Q33984484-4BBE58EA-5F9F-4DC5-92A3-135D023F63D2Q36261965-DBCCFF17-FFD4-4BC0-88F5-495BB2C0E2A5Q43254124-FA43415F-4D66-4A90-87E5-ABC8135FCD1AQ43258325-2EAC645D-2039-4062-87C0-8D635441649BQ43754403-DA66EF9E-E8D4-499F-9CD2-AF899690F458Q43795520-018348F9-BDF4-4272-9AB9-9EF58E0E842AQ43868144-AFE269FF-07B1-41D7-8916-0B76BEF13946Q44775732-F1BD5C62-6A6E-4E21-BB81-5279A1D703B1Q44837897-AC4AE693-EC08-4C28-B4D0-20FEB42FEDB0Q44986332-F6F64F1A-C7AC-4ED4-88ED-B7C50E78F19FQ45017691-B7DD48C4-C909-4A48-A818-B4BE7477B8C6Q45036114-6EE44A08-3F76-4A3C-ACEB-B746B4B2FA6CQ45082672-6A933844-F246-4671-8BB5-91818969CD8EQ46083080-4987F8B7-172B-47F8-A09B-796D1A13798EQ46305587-7252EE26-4873-43B1-B9D9-7B2F3C2B6A5DQ46913719-A9D76430-85E4-45A5-A08A-446F1406CECDQ47802342-AA1EB3A8-1437-4985-87DB-711B8E564C3EQ54133591-0E682C47-14B3-46D5-AD36-A34EB2C41136Q54381744-A0B0887E-A91C-4F59-B802-680CAE477FE3Q56209526-6E2DAFD8-4EE4-4B4D-9E15-BA20E048AD97Q60452868-23A415FF-7BC2-4E2B-B9B7-DC11B6B00223Q60452869-C973976E-97DF-4D0B-B11C-E734FCC3DFEDQ60452875-DFA6E63D-7A75-4CE7-B521-877D125A8C87Q62509024-80305BD6-3824-479C-AF9F-104A0856F10DQ62509049-0FDB850E-A41F-4676-B818-B0596DD14703Q62509052-FF545E0A-EC0B-4715-939C-BA709946F37EQ62509060-747F3180-0286-4416-8DD5-0270C2D8FC53Q62683339-43500C6C-17AC-40F2-8BB0-27CAABF529D3Q63532799-C36EA4E0-4F0D-4B87-AC91-22E888B6A6DFQ63532800-F957B7C2-123E-4517-9301-9D62CFE3DCB7Q63532801-F1737E2F-DCCC-4530-B227-D59F7764C968Q70271632-7736B754-3459-42EF-8B92-37D1A052D62BQ72858683-BE10F1A6-6F8A-452E-87A3-6F39910AB01AQ72869026-4D31DDF1-219E-4046-B639-367250506FA5Q72916225-C1777121-D16A-451E-B229-35DB100CDD3CQ73450637-E6B04EA5-D522-4BAB-9B9D-69C44671D372
P50
description
Ameerika Ühendriikide keemik
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American chemist
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Amerikaans scheikundige
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US-amerikanischer Chemiker
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Usana kemiisto
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amerikansk kemiker
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amerikansk kemist
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amerikansk kjemikar
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amerikansk kjemiker
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ceimiceoir Meiriceánach
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John Brauman
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John Brauman
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John Brauman
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John I. Brauman
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John I. Brauman
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John I. Brauman
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John I. Brauman
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John I. Brauman
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John I. Brauman
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John Brauman
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John Brauman
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John I. Brauman
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John I. Brauman
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John I. Brauman
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John I. Brauman
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John I. Brauman
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John I. Brauman
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John I. Brauman
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John Brauman
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John Brauman
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John Brauman
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John Brauman
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John Brauman
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John Brauman
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John I. Brauman
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John I. Brauman
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John I. Brauman
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John I. Brauman
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John I. Brauman
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John I. Brauman
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John I. Brauman
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P1006
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