about
Structural and mechanistic studies of polymerase bypass of phenanthriplatin DNA damageThe Next Generation of Platinum Drugs: Targeted Pt(II) Agents, Nanoparticle Delivery, and Pt(IV) ProdrugsReinterpretation of the vibrational spectroscopy of the medicinal bioinorganic synthon c,c,t-[Pt(NH3)2Cl2(OH)2].Pt(IV) prodrugs designed to bind non-covalently to human serum albumin for drug deliveryEffects of monofunctional platinum agents on bacterial growth: a retrospective study.Understanding and improving platinum anticancer drugs--phenanthriplatinEncapsulation of Pt(IV) Prodrugs within a Pt(II) Cage for Drug Delivery.Beyond iron: non-classical biological functions of bacterial siderophoresNanoparticle encapsulation of mitaplatin and the effect thereof on in vivo propertiesMonofunctional and higher-valent platinum anticancer agents.A Potent Glucose-Platinum Conjugate Exploits Glucose Transporters and Preferentially Accumulates in Cancer Cells.Necroptosis-inducing rhenium(V) oxo complexes.Bidentate ligands on osmium(VI) nitrido complexes control intracellular targeting and cell death pathways.Nucleotide Binding Preference of the Monofunctional Platinum Anticancer-Agent Phenanthriplatin.Chemical Synthesis of Staphyloferrin B Affords Insight into the Molecular Structure, Iron Chelation, and Biological Activity of a Polycarboxylate Siderophore Deployed by the Human Pathogen Staphylococcus aureus.The Crystal Structure of Oxaliplatin: A Case of Overlooked Pseudo Symmetry.The chiral potential of phenanthriplatin and its influence on guanine binding.A breast cancer stem cell-selective, mammospheres-potent osmium(VI) nitrido complexQuantifying the efficiency of CO2 capture by Lewis pairs.Improvements in the Synthesis and Understanding of the Iodo-bridged Intermediate en Route to the Pt(IV) Prodrug Satraplatin.Oxidative halogenation of cisplatin and carboplatin: synthesis, spectroscopy, and crystal and molecular structures of Pt(IV) prodrugs.Synthesis and oxidation of phosphine cations.Determination of the Molecular Structures of Ferric Enterobactin and Ferric Enantioenterobactin Using Racemic Crystallography.Hydroboration of Phosphaalkynes by HB(C6 F5 )2.1,1-Hydroboration and a Borane Adduct of Diphenyldiazomethane: A Potential Prelude to FLP-N2 Chemistry.Catalytic double hydroarylation of alkynes to 9,9-disubstituted 9,10-dihydroacridine derivatives by an electrophilic phenoxyphosphonium dication.Dicationic phosphonium salts: Lewis acid initiators for the Mukaiyama-aldol reaction.Accessing Frustrated Lewis Pair Chemistry from a Spectroscopically Stable and Classical Lewis Acid-Base AdductAccessing Frustrated Lewis Pair Chemistry from a Spectroscopically Stable and Classical Lewis Acid-Base AdductProbing steric influences on electrophilic phosphonium cations: a comparison of [(3,5-(CF3)2C6H3)3PF]+ and [(C6F5)3PF]+The global electrophilicity index as a metric for Lewis acidityA model for C–F activation by electrophilic phosphonium cationsFrustrated Lewis Pair Oxidation Permits Synthesis of a Fluoroazaphosphatrane, [FP(MeNCH2CH2)3N]+Improving the Global Electrophilicity Index (GEI) as a Measure of Lewis AcidityHydrogen-bonding asymmetric metal catalysis with alpha-amino acids: a simple and tunable approach to high enantioinductionElectrophilic phenoxy-substituted phosphonium cationsCationic aluminum hydride complexes: reactions of carbene-alane adducts with trityl-borateUsing frustrated Lewis pairs to explore C-F bond activation
P50
Q27684330-EF3C0119-CF29-419F-90E4-D03780E7DFADQ28066801-2338A92D-4EC4-4185-A046-22EFE74171A1Q33650926-0863EC4D-B15B-4255-8D94-F7C67702F211Q33825880-D155E05C-0D58-452A-AAE4-7B46FC7D4D9AQ34393918-F88FF133-6297-4876-84FD-18EC12F7B81BQ34396623-37AE504D-BDDE-44F4-97BC-0A5FAB45DCBCQ35000093-36C7637D-3F01-429B-9D29-3D380B7EB89EQ35220353-FC12B10A-5BBF-40B1-9244-30F8B56F8BAAQ37042860-E3008C65-D750-4DB9-9336-D313A3FE1013Q37282213-DB1E5FB0-3930-4409-8DE0-AC329A8FF080Q38411327-F458082F-7DB3-49C8-8810-94479BA5F383Q38907938-0706CE20-C6B5-4BEF-AA67-7F564D3E0B67Q39095158-F0D13939-E4C1-41D3-945E-C653CDCC7223Q39824889-17CBDF85-2BB9-47EB-B5CE-CDF37DF39DB2Q41192825-B9BE4B21-C0A9-4044-A012-D463E9845479Q41859715-5FED0FD1-9ECC-455C-89AA-B1999590D32AQ41984036-A939A6A4-EE4A-49DB-B95A-F25A0F56ED89Q42113076-5DEBB1B2-F2EA-41BC-A0BB-8BA7F13065D7Q42280611-B1A09DDC-3748-4A29-9B5B-02452432FE6DQ43029692-178C4369-9589-432B-AF07-790464925044Q43051494-9E6CEF18-E4FE-4C2E-96ED-885B25702EC9Q46294167-C02DF452-DB42-458E-A275-626AC371A5F9Q47731915-661FFB4C-066B-4A8E-A828-2EEB5248904EQ48175739-393E43A2-05F6-4BDC-AA7C-B8E24F607F78Q48357790-B267CCC3-462A-41C2-A3A6-D5D53E7CF7A1Q50007006-54935E23-0666-45D8-930B-A900F3D9B674Q50040442-EE0FBCF7-8327-4538-813C-0209688E2BE7Q57394653-CF54A79B-26B3-48E2-8882-97C7CB9511EBQ57394655-E1C8062C-E3A0-487C-B69A-FAC3C2BB0497Q57394672-6F385CC0-ABA9-4C46-9C10-B3A905D6DFA8Q57394675-B5B29F36-5107-49EF-A6AB-F4A96396BE13Q57394684-CB701869-BDA3-4379-86DD-20224E7C4862Q60338025-12C6C1E5-3991-4C4C-8210-3AD8A33A5C1AQ60338029-900AEF37-C34B-48A4-8787-346230D962F5Q84288570-2A10FA88-A93F-4720-BCD1-C4D73A27CF53Q88634795-446B3572-3AA6-4A41-97D9-7FE99F518A85Q89035324-DA68793E-8957-47E0-8382-A4C842747EDEQ92488299-ECEA21B7-8B67-4F51-8210-FD74714EF730
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Timothy C Johnstone
@ast
Timothy C Johnstone
@en
Timothy C Johnstone
@es
Timothy C Johnstone
@fr
Timothy C Johnstone
@sl
type
label
Timothy C Johnstone
@ast
Timothy C Johnstone
@en
Timothy C Johnstone
@es
Timothy C Johnstone
@fr
Timothy C Johnstone
@sl
altLabel
Timothy C. Johnstone
@en
prefLabel
Timothy C Johnstone
@ast
Timothy C Johnstone
@en
Timothy C Johnstone
@es
Timothy C Johnstone
@fr
Timothy C Johnstone
@sl
P106
P21
P31
P496
0000-0003-3615-4530