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Method for the computational comparison of crystal structuresSupervised Self-Organizing Maps in Crystal Property and Structure PredictionIrII(ethene): metal or carbon radical?beta -Helical polymers from isocyanopeptides.Report on the sixth blind test of organic crystal structure prediction methods.Molecular recognition and self-assembly special feature: Squaring cooperative binding circles.Searching for stereoisomerism in crystallographic databases: algorithm, analysis and chiral curiosities.High nuclearity manganese(III) compounds containing phenol-pyrazole ligands: the influence of the ligand on the core geometry.Ligand-controlled magnetic interactions in Mn(4) clusters.Molecular clips based on propanediurea: exceptionally high binding affinities for resorcinol guests.Lamellar organic thin films through self-assembly and molecular recognition.(+/-)-Schefflone: a trimeric monoterpenoid from the root bark of Uvaria scheffleri.Amidopalladation of alkoxyallenes applied in the synthesis of an enantiopure 1-ethylquinolizidine frog alkaloid.Efficient preparation of a 1,3-diazidocyclitol as a versatile 2-deoxystreptamine precursor.Enantioselective BINOL-phosphoric acid catalyzed Pictet-Spengler reactions of N-benzyltryptamine.Fully orthogonally protected 2-deoxystreptamine from kanamycin.Ligand conformation enforces trigonal bipyramidal coordination geometry in a new dinuclear bis(pyrazolato)-bridged copper(II) complex: synthesis, crystal structure, and properties of [Cu(Npy2pz)]2(ClO4)2.2CH3CN.The hydration/dehydration behavior of aspartame revisited.Uncorrelated dynamical processes in tetranuclear carboxylate clusters studied by variable-temperature 1H NMR spectroscopy.Polymorphism and Modulation of Para-Substituted l-Phenylalanine.Racemic and Enantiopure Camphene and Pinene Studied by the Crystalline Sponge Method.Processive rotaxane systems. Studies on the mechanism and control of the threading process.Representing structural databases in a self-organizing map.Powder pattern indexing using the weighted crosscorrelation and genetic algorithms.Tomato-produced 7-epizingiberene and R-curcumene act as repellents to whiteflies.Formal Synthesis of Solanoeclepin A: Enantioselective Allene Diboration and Intramolecular [2+2] Photocycloaddition for the Construction of the Tricyclic Core.Carbonyl Complexes of Rhodium with N-Donor Ligands: Factors Determining the Formation of Terminal versus Bridging CarbonylsAmido-bridged dinuclear rhodium(I) complexes by deprotonation of mononuclear rhodium(I) amine complexesSpontaneous disproportionation of rhodium(i) bisoxazolinates to rhodium(ii)Electronic supplementary information (ESI) available: synthetic procedures (including 1H NMR, 13C NMR and elemental analysis data), EPR spectrum and cyclic voltammogram. See hOxidation of RhI(olefin) Fragments to 2-Rhoda(III)oxetanesX-Ray Spectroscopic and Diffraction Study of the Structure of the Active Species in the NiII-Catalyzed Polymerization of IsocyanidesCarbenoid transfer reactions catalyzed by a ruthenium porphyrin macrocycleEnantioselective Approach to the Right-Hand Substructure of Solanoeclepin ASecuring Important Strigolactone Key Structures: Orobanchol and 5-DeoxystrigolStabilisation of 2,6-Diarylpyridinium Cation by Through-Space Polar-π InteractionsStrong Induced-Fit Binding of Viologen and Pyridine Derivatives in Adjustable Porphyrin CavitiesThermodynamics and kinetics of guest-induced switching between "basket handle" porphyrin isomers.Antiplasmodial and cytotoxic activities of Striga asiatica and Sauropus spatulifolius extracts, and their isolated constituentsLigand effects of NHC–iridium catalysts for signal amplification by reversible exchange (SABRE)Enantioselective Organocatalytic Thiol Addition to α,β-Unsaturated α-Amino Acid Derivatives
P50
Q27061962-FBBC5854-DBBB-4A64-BAB3-BC3342E684E7Q27134724-22A70DF6-E176-42FB-8E2B-6C39F9D5FF79Q28306569-9053BA92-5794-45D6-8A18-85BB631C72B0Q30657350-B2145890-F969-494E-903A-F2745B148C4CQ34536112-95DE9819-4805-4851-97FC-1D7BE88A7D21Q37250008-7E86E934-180B-4176-A11A-1535C89931DFQ38749946-879684F2-46CC-47E1-BD43-2AE61679E511Q42742849-82ABA69F-D63B-43A2-806E-53E804DC2614Q43241450-F6FD9886-6399-4D73-B3A9-83F4CB3CE9FDQ43576288-F79F034B-B0D6-47DE-BE5A-3117CEFD0DE8Q43655974-7B8ABAC6-5DEF-4271-A57D-12BE40C3771EQ43948980-318EEEFD-0B83-40F8-8827-46744E48F2B7Q44821574-CA9CE8EC-1BFF-43F5-B88E-F21C71645C3CQ44940893-83A08A94-0892-4B5C-A6D0-C44A678E4AC4Q46491476-5DD53316-80DF-4AA3-B9C8-9BDBEE571281Q46560738-16E3DE5C-EB11-4BC6-8B72-9BE1992545D0Q46767324-6CE2E441-EF17-40BF-930D-9A82C3CF9811Q46799206-70283C7C-5349-4273-B197-D8D99063655AQ46976820-8378A43C-357F-40B1-94F1-65AD412596B1Q47098419-B0C12084-DA7D-4D77-8660-E4EC8DD61069Q47162200-FE2979BD-FC2D-4B47-A0C3-2CD3D67CEB42Q51917841-3AF221BA-7354-41C3-B44C-E6A34A503888Q51963701-65C91367-49D3-4EFA-BE8C-F37A0BA025C6Q52016453-B6D107C6-4A79-49EC-BD7D-F32F1581B1DBQ52712163-51D4C47B-5F7F-4FD3-9235-1E1BBD520509Q53181916-1536EB0E-205E-487A-995F-B6DC4C1237C3Q56743817-B4CE7044-9B9C-4C0B-9CF6-4869962178A1Q56744650-641C7001-9956-408B-9490-6F1DC5C502ABQ56744738-9A8CADEA-DD3C-45F7-A917-CE6E52310E62Q56744906-023A2CC0-9C06-40A3-8A7D-4FD5F681E61FQ57597251-89DFED78-A7D4-47FF-A759-C5F6DBE865EDQ57836176-4C2CC758-2BC8-4096-9112-4DD6AB95A0C3Q57836178-D66A5BD3-8317-44A5-965E-0D16BAC05DF6Q57836179-3E6D0B50-254D-4086-9B78-A5DAD3677425Q57836181-40C2FEDD-ECF6-49D3-BDBE-115644CD53A7Q57836182-9DB7E061-C16D-46F8-8EEC-C74A4DC54BD5Q57836183-1AFFFC45-81C2-498F-8838-0A536345D687Q57836185-BCA13935-499E-44CF-971D-49A4F0F0A5CBQ57836186-A7DF4C4F-D32F-4869-B5B7-AC2C4E958302Q57836187-CDF9BC20-A873-44AC-9497-19B8B14AB25A
P50
description
crystallographer at Radboud University
@en
wetenschapper
@nl
name
René de Gelder
@ast
René de Gelder
@en
René de Gelder
@es
René de Gelder
@nl
René de Gelder
@sl
type
label
René de Gelder
@ast
René de Gelder
@en
René de Gelder
@es
René de Gelder
@nl
René de Gelder
@sl
altLabel
R. de Gelder
@en
Rene de Gelder
@en
de Gelder R
@en
prefLabel
René de Gelder
@ast
René de Gelder
@en
René de Gelder
@es
René de Gelder
@nl
René de Gelder
@sl
P1053
D-4587-2012
P106
P21
P31
P3829
P496
0000-0001-6152-640X