about
A facile route to functionalized N-heterocyclic carbenes (NHCs) with NHC base-stabilized dichlorosilylene.Reaction of N-heterocyclic silylenes with thioketone: formation of silicon-sulfur three (Si-C-S)- and five (Si-C-C-C-S)-membered ring systems.Nickel-catalysed direct C2-arylation of N-heterocyclic carbenes.Silylene-Functionalized N-Heterocyclic Carbene (Si-NHC).Carbon-based two electron σ-donor ligands beyond classical N-heterocyclic carbenes.N-Heterocyclic Vinylidene-Stabilized Phosphorus Biradicaloid.Classical N-Heterocyclic Carbenes Derived Crystalline Radicals.The Viability of C5-Protonated- and C4,C5-Ditopic Carbanionic Abnormal NHCs: A New Dimension in NHC Chemistry.Palladium-catalyzed direct C2-arylation of an N-heterocyclic carbene: an atom-economic route to mesoionic carbene ligands.Facile routes to abnormal-NHC-cobalt(ii) complexes.Mixed valence η6-arene cobalt(I) and cobalt(II) compound.Donor-acceptor-stabilized silicon analogue of an acid anhydride.Kekulé diradicaloids derived from a classical N-heterocyclic carbene.Facile Access to Transition-Metal-Carbonyl Complexes with an Amidinate-Stabilized Chlorosilylene LigandConvenient Access to Monosilicon Epoxides with Pentacoordinate SiliconLewis-Base-Stabilized Dichlorosilylene: A Two-Electron σ-Donor LigandLewis Base Stabilized DichlorosilyleneAn access to base-stabilized three-membered silicon heterocyclesLewis base mediated dismutation of trichlorosilaneN-Heterocyclic Carbene Stabilized Dichlorosilylene Transition-Metal Complexes of V(I), Co(I), and Fe(0)Neutral pentacoordinate silicon fluorides derived from amidinate, guanidinate, and triazapentadienate ligands and base-induced disproportionation of Si2Cl6 to stable silylenesStabilization of low valent silicon fluorides in the coordination sphere of transition metalsA dimer of silaisonitrile with two-coordinate silicon atomsDonor-acceptor stabilized silaformyl chlorideFree radical reactivity of mono- and dichlorosilylene with muoniumAmbiphilicity of dichlorosilylene in a single moleculeFacile access to silyl-functionalized N-heterocyclic olefins with HSiCl3Mono- and di-cationic hydrido boron compoundsSelective functionalization of a bis-silyleneStable silaimines with three- and four-coordinate silicon atomsSynthesis and structural investigation of R2Si (R = Me, Ph) bridged di-N-heterocyclic carbenesNormal-to-abnormal rearrangement of an N-heterocyclic carbene with a silylene transition metal complexN-Heterocyclic Carbene Analogues of Thiele and Chichibabin HydrocarbonsIsolation of singlet carbene derived 2-arsa-1,3-butadiene radical cations and dicationsCrystalline Divinyldiarsenes and Cleavage of the As=As BondCrystalline Divinyldiarsene Radical Cations and DicationsDirect functionalization of white phosphorus with anionic dicarbenes and mesoionic carbenes: facile access to 1,2,3-triphosphol-2-idesDiradical Character Enhancement by Spacing: N-Heterocyclic Carbene Analogues of Müller's HydrocarbonA Phosphorus Analogue of p-Quinodimethane with a Planar P4 Ring: A Metal-Free Diphosphorus SourceElectrophilic terminal arsinidene-iron(0) complexes with a two-coordinated arsenic atom
P50
Q42979049-B60C74AB-7046-4347-BF9E-81171F3759D4Q45114675-0D41C702-340E-4F9C-95D7-0A23E6D21753Q46314620-D4EE25FC-F8DC-4B08-9D7A-D7C85D2E7001Q48191177-753297E8-722B-4FEC-A08D-DE2792A71214Q48297432-25145D6A-BF97-4528-B6D4-F61E583DFC81Q48360455-933DF21A-5053-4C6C-BC58-CC2B3C7B32B1Q49710312-E4FC9C75-8482-4F2E-A3BD-0F356642A5C2Q49830759-BB643DDE-7346-4844-80C5-4904F21873ECQ51012832-0F29074C-4DC4-4DFB-BBEC-5E645E7D80FCQ52626431-021727B6-BC3C-4F0E-885D-C827626157C9Q53104143-D654957A-28B1-4946-8DEA-6818B51596A9Q53909109-EE27F6BA-A59B-4DE4-9892-AE647B070228Q55340046-1EE5C316-FA20-4C53-9E6F-71DB47E516A0Q57905728-AEC11710-B887-48B0-B998-1CE1E363155FQ57905912-64587AEB-9E00-4CC0-954F-368EC63B5CA4Q57905923-753258FA-C86F-4D62-98C0-FB838B8199A5Q57905969-021BA6D9-EE5B-4FDB-8118-D19382CF5580Q61940411-1BD64349-7469-4547-8ABC-C4804A059F9BQ61940413-BCB05611-A201-4388-A604-6D323872EE3EQ61940418-84C625F1-7A90-4F7C-BDF9-2D671513C602Q82707783-86E4CC3E-9F77-46AA-B1F3-F1301C16ED3CQ83106166-33C96ED5-FB56-47F1-97CF-38E35BE4C175Q84108075-88DA3B30-F0C4-405F-A2F6-41F437B0E479Q84564983-04EE8656-3871-423C-AE4B-0229B65F23DFQ84922962-9EE12255-7709-4CC4-A0D3-97FEED5DBF0EQ84966717-C59624C9-70F4-4586-8D88-F93769AF5B76Q85636591-B8F2C170-1BF3-4622-9E0A-0B99657EFFABQ85640856-DDE9E41B-79D0-4F3A-9F3F-C2EBE71C5BFFQ86865448-C81BFBF7-3DD9-4EC7-B43B-621DA794A7C2Q87409803-452DAD8D-A748-4B16-B415-64C6C57A970BQ87519142-D6732571-2D6B-4412-B60B-1400BBD0124EQ88256253-90EC779C-BB5B-495C-9148-9646A66DD3DBQ88396362-BD509A3A-1750-48E6-AE93-AEFCCBCC2902Q89912597-018337EE-CADF-406B-95A6-C7D2D2A50D56Q90270344-BAA4DD4D-37A9-42E1-A4DA-B0B2D21935CBQ90278502-22021A45-4203-4049-9070-EC3CA26B1CF2Q90609640-64275598-17FE-45E5-9B50-AC246B82EE5EQ91313071-0F1199DD-254D-4502-9B37-1D8789EBBE12Q91332541-ABA04487-C0FA-46F8-8CAD-F5085C693D74Q91353674-AE34671B-E5A3-4893-B28E-6E4B3DFB0521
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Rajendra S Ghadwal
@nl
Rajendra S Ghadwal
@sl
Rajendra S. Ghadwal
@en
Rajendra S. Ghadwal
@es
type
label
Rajendra S Ghadwal
@nl
Rajendra S Ghadwal
@sl
Rajendra S. Ghadwal
@en
Rajendra S. Ghadwal
@es
prefLabel
Rajendra S Ghadwal
@nl
Rajendra S Ghadwal
@sl
Rajendra S. Ghadwal
@en
Rajendra S. Ghadwal
@es
P108
P106
P1153
6507986161
P31
P496
0000-0003-2146-5432