about
Anticancer activities of self-assembled molecular bowls containing a phenanthrene-based donor and Ru(II) acceptors.Synthesis of chlorinated bicyclic C-fused tetrahydrofuro[3,2-c]azetidin-2-ones.Synthesis and reactions of ethynylferrocene-derived fluoro- and chlorocyclotriphosphazenes.Coordination-Driven Self-Assembly of Heterotrimetallic Barrel and Bimetallic Cages Using a Cobalt Sandwich-Based Tetratopic Donor.Selective synthesis of iridium(iii)-derived molecular Borromean rings, [2]catenane and ring-in-ring macrocycles via coordination-driven self-assembly.Coordination-Driven Self-Assembly and Anticancer Potency Studies of Ruthenium-Cobalt-Based Heterometallic Rectangles.Coordination-Driven Self-Assembly Using Ditopic Pyridyl-Pyrazolyl Donor and p-Cymene Ru(II) Acceptors: [2]Catenane Synthesis and Anticancer Activities.Selective Synthesis of Molecular Borromean Rings: Engineering of Supramolecular Topology via Coordination-Driven Self-Assembly.Ring-closing metathesis reactions of terminal alkene-derived cyclic phosphazenesPalladacycles of novel bisoxazoline chelating ligands based on the dimeric cyclobutadiene linked cobalt sandwich compound [(η5-Cp)Co(η4-C4Ph3)]2Reactions of alkyne- and butadiyne-derived fluorinated cyclophosphazenes with diiron and dimolybdenum carbonylsProtecting group directed diversity during Mitsunobu cyclization of a carbohydrate derived diamino triol. Synthesis of novel bridged bicyclic and six-membered iminocyclitolsCoordination-driven self-assembly of an iridium-cornered prismatic cage and encapsulation of three heteroguests in its large cavityTemplate-Free Synthesis of a Molecular Solomon Link by Two-Component Self-AssemblySelective synthesis of ruthenium(II) Metalla[2]catenane via solvent and guest-dependent self-assemblyCoordination-Driven Self-Assembly of a Molecular Knot Comprising Sixteen Crossings
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Q36010364-29A6A129-CF58-4316-9D60-9E96295835B1Q42875593-ED7DF7A5-A9B1-4990-ACD9-1B321844121DQ43052829-A1423D4C-0C48-4158-AED2-4646A5490082Q47214052-B41D0F29-F4E1-4D28-8C05-DED154C5B6C9Q48051916-27AF70B0-D406-49D2-9D1D-2BB7EFC14F50Q48053815-2FBF8422-50B2-4B7B-9D4E-E89DBFB8F452Q48058661-58F0F80D-B354-45E5-AB68-47B39641C3ECQ51281593-3F4DFE00-B6D8-48A2-BC55-6420C33512F3Q82650329-BB414C6B-CC21-45B4-AC08-E8854E7E1EA2Q83641119-D73518D9-6794-475D-9C0F-5C0A94523913Q85292662-93815676-E21A-419A-8695-0E7D6437A553Q85600446-EAE66B87-34DA-4766-8A40-D1456C115EBCQ86734027-7FB21C7A-7126-40B7-8743-EF8693DC744EQ86983275-32E18043-A511-471D-90EE-F71CA49F0047Q87018504-15737F98-643F-4B38-A81D-DFD39CE1884EQ88142700-4A77C946-07F2-47F9-B8E7-DC287F472387
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Nem Singh
@en
Nem Singh
@nl
type
label
Nem Singh
@en
Nem Singh
@nl
prefLabel
Nem Singh
@en
Nem Singh
@nl
P31
P496
0000-0003-2952-3385