about
Group 4 salicyloxazolines are potent polymerization catalysts.Chiral metallohelices enantioselectively target hybrid human telomeric G-quadruplex DNA.Chiral semiconductor phases: the optically pure D3[M(III)(S,S-EDDS)]2 (D=TTF, TSF) family.The Synthesis and STM/AFM Imaging of ‘Olympicene’ Benzo[cd]pyrenesOptically pure, water-stable metallo-helical 'flexicate' assemblies with antibiotic activity.Asymmetric triplex metallohelices with high and selective activity against cancer cells.Anticancer metallohelices: nanomolar potency and high selectivity.Antifreeze Protein Mimetic Metallohelices with Potent Ice Recrystallization Inhibition Activity.Shape-selective recognition of DNA abasic sites by metallohelices: inhibition of human AP endonuclease 1.Mechanism of catalytic cyclohydroamination by zirconium salicyloxazoline complexes.fac-Specific syntheses of homochiral [Fe(NN)3]2+ complexes (NN = pyridine keto-hydrazone); origins of the stereoselectivity.Organic-soluble optically pure anionic metal complexes PPh4[M(III)(S,S-EDDS)].2H2O (M = Fe, Co, Cr).Chirality and diastereoselection in the mu-oxo diiron complexes L(2)Fe-O-FeL(2) (L = bidentate salicylaldiminato).Enantioselective aziridination using copper complexes of biaryl Schiff bases.Considerations of noise and measurement reproducibility of circular dichroism measurements using Na[CoIII(EDDS)].Chiral biarylamido/anisole complexes of yttrium in enantioselective aminoalkene hydaroamination/cyclisation.Arylaminopyridinato complexes of zirconium.Aminooxazolinate; a chiral amidinate analogue.Chiral metal architectures in aminopyridinato complexes of zirconium.Structural and electronic modulation of magnetic properties in a family of chiral iron coordination polymers.Self-assembling optically pure Fe(A-B)3 chelates.Awakening a dormant catalyst: salicylaldimine systems for ethene/tert-butylstyrene copolymerization.A new reference material for UV-visible circular dichroism spectroscopy.Constrained geometry aminooxazolinate ligands giving chiral zirconium guanidinates; catalytic cyclohydroamination.Chiral metallohelical complexes enantioselectively target amyloid β for treating Alzheimer's disease.Stereochemistry and amyloid inhibition: Asymmetric triplex metallohelices enantioselectively bind to Aβ peptide.Metallohelices: potential mimetics of α-helical peptides in cancer treatment?Optically pure heterobimetallic helicates from self-assembly and click strategies.Biaryl amine ligands for lanthanide catalysed enantioselective hydroamination/cyclisation of aminoalkenesMetallohelices with activity against cisplatin-resistant cancer cells; does the mechanism involve DNA binding?Dalton Discussion 12: Catalytic C–H and C–X bond activation (DD12)End-functional polyolefins for block copolymer synthesisMirror-Image Dependence: Targeting Enantiomeric G-Quadruplex DNA Using Triplex MetallohelicesPolyolefin–Polar Block Copolymers from Versatile New MacromonomersAntimicrobial MetallodrugsIron and Manganese Complexes of 2-Carbonyl Pyrrolyls: Scorpionate Sandwich Anions and Extended StructuresAll about the arrowJahn–Teller effects on π-stacking and stereoselectivity in the phenylethaniminopyridine tris-chelates Cu(NN′)32+Approaches to the synthesis of optically pure helicatesComments on “Synthesis and characterisation of enantiopure copper(ii) complexes with chiral bidentate ligands”
P50
Q31014624-2B0FFFFA-AFA7-4729-8281-A7C3A917F398Q33701380-ECFB8C80-C622-4F03-AD4D-D01D8287B221Q33861901-DC59CFA5-12E9-4BD7-88B6-958E6747BA59Q33959199-DE79A6A1-6285-405A-BE64-32E461BA9356Q34101281-2718E609-7E30-4F66-ACF8-CEE6905831B2Q35229082-154F4701-E764-4188-B4F1-2DCD4DE4D5E1Q41148942-16CD447D-EE3E-456D-A228-3D32C3103B4CQ41456611-332F1432-B07E-415B-B143-F08858F174DFQ42410846-6559BEF1-1608-4634-881C-DC1F001F5D40Q42861320-162F265D-2D0E-452F-84D8-F14097F9932FQ43112594-01384590-CC18-4293-A470-F515DEC6B6D8Q43143624-1862F0C6-1144-48FC-AC99-70110CF635CAQ43159661-EB8E600D-2EC8-458C-A682-0C93092333FFQ43988316-B29CC8C7-2011-44D2-AF06-C45ACABE723DQ44586497-B5807FCA-3094-4627-ABF1-F928517742C4Q44996191-5D29ECA8-B2A5-4E6F-A201-16AFB3678FAFQ44996193-C7E09FD1-4DB0-44FF-AC65-AD023A2884F8Q45150344-7CD8D178-92D3-4C67-A172-40188546132EQ45159139-0D20D974-A282-4A44-ADCD-27E991C62AFBQ45200558-83456B64-CEFC-46CE-A6E2-B7C40477BE31Q46084841-9F951B1B-59CA-421E-88B2-CD01360A4D6BQ46218359-9855AE62-D370-4B9C-8AB4-C76126DA8C15Q46572540-58E0A76A-CCE8-4FDB-8838-EFF4A517C48FQ46584637-60D8FF8C-2620-4416-A4A4-B487661568B4Q46861176-32A53EC3-8BD6-460E-9D09-C44AC96C180FQ48161785-D2D44008-E72A-4282-8ACB-1CEF725240ADQ48635500-5EEC3C84-B870-4FF1-8BFA-CAB398182FCFQ51791240-1637D205-4203-497C-A9E1-5D943BCA999EQ56639242-F27F11C4-0771-472E-A00A-E3EE8E23C644Q57393638-00BC9C00-AB7C-4007-BEC7-0291945DAA72Q60318529-C5DAA571-21C2-441B-8922-883DC1C35D7AQ63350479-C2BE1226-C20C-406E-A279-445D398BAF35Q63350480-C7D7D39A-456B-4C00-9122-05147D54E769Q63350481-8A6D7C30-F0BC-46D3-AE98-53993867B15DQ63350482-2BF5F65D-A18C-4ACE-8473-92F6F8AF2EF8Q63350483-BC0D0B07-CC0B-44E1-A8D8-B5E3FE3893B8Q63350484-A2FE3C33-04DC-414A-9B7C-4BDA0FC2CF86Q63350485-6A8CA657-2E65-4790-9C33-5A9F9670714DQ63350486-267BE759-FBFF-449A-BC01-63545076E37AQ63350487-170CB9F4-F99F-4040-8604-BF88B78A0F30
P50
description
researcher
@en
հետազոտող
@hy
name
Peter Scott
@ast
Peter Scott
@en
Peter Scott
@es
Peter Scott
@nl
Peter Scott
@sl
type
label
Peter Scott
@ast
Peter Scott
@en
Peter Scott
@es
Peter Scott
@nl
Peter Scott
@sl
prefLabel
Peter Scott
@ast
Peter Scott
@en
Peter Scott
@es
Peter Scott
@nl
Peter Scott
@sl
P1053
D-2029-2010
P106
P21
P31
P3829
P496
0000-0002-5656-7060