about
Design, synthesis and crystallographic analysis of nitrile-based broad-spectrum peptidomimetic inhibitors for coronavirus 3C-like proteasesProfiling of substrate specificity of SARS-CoV 3CLExpanding the gelation properties of valine-based 3,5-diaminobenzoate organogelators with N-alkylurea functionalities.Profiling of substrate specificities of 3C-like proteases from group 1, 2a, 2b, and 3 coronaviruses.A supramolecular ladder polymer prepared by hydrogen bonding-mediated self-assembly of a metallomacrocycle.Conformational and supramolecular properties of main chain and cyclic click oligotriazoles and polytriazoles.Structural effects on the catalytic, emulsifying, and recycling properties of chiral amphiphilic dendritic organocatalysts.Synthesis of organoplatinum poly(dendrimer)s: pronounced effect of size and geometry of small organoplatinum linkers on the copolymerization efficiency with bifunctional dendritic macromonomers.Transition from low molecular weight non-gelating oligo(amide-triazole)s to a restorable, halide-responsive poly(amide-triazole) supramolecular gel.Click-dendronized poly(amide-triazole)s--effect of dendron size and polymer backbone symmetry on self-assembling and gelation properties.Tribenzotriquinacene-Based Crown Ethers: Synthesis and Selective Complexation with Ammonium Salts.Different Gelation and Self-Sorting Properties of Two Isomeric Polyamides Owing to the Parallel versus Anti-Parallel Alignment of Backbone Dipoles.From Fenestrindane towards Saddle-Shaped Nanographenes Bearing a Tetracoordinate Carbon Atom.A platinum(II) terpyridine metallogel with an L-valine-modified alkynyl ligand: interplay of Pt⋅⋅⋅Pt, π-π and hydrogen-bonding interactions.Versatile syntheses of hemi-cryptophanes and a metallo-cryptophane from a hexa-functionalized C3v -symmetrical tribenzotriquinacene (TBTQ) derivative.o-Quinones Derived from Tribenzotriquinacenes: Functionalization of Inner Bay Positions and Use for Single-Wing Extensions.Facile Assembly of Chiral Metallosquares by Using Enantiopure Tribenzotriquinacene Corner Motifs.Biconcave and Convex-Concave Tribenzotriquinacene Dimers.Halogen-Bond-Mediated Assembly of a Single-Component Supramolecular Triangle and an Enantiomeric Pair of Double Helices from 2-(Iodoethynyl)pyridine Derivatives.Trefoil-Shaped Porous Nanographenes Bearing a Tribenzotriquinacene Core by Three-fold Scholl MacrocyclizationHydrophobically Modified Dendrons: Developing Structure−Activity Relationships for DNA Binding and Gene TransfectionSynthesis and Self Assembling Properties of Rod-Like, 2-Ureido-4-pyrimidinone-Based Main Chain Supramolecular Dendronized PolymersGeneration-Independent Dimerization Behavior of Quadruple Hydrogen-Bond-Containing Oligoether DendronsA Polycyclic Aromatic Hydrocarbon Bearing an All-cis Tetrabenzo[5.5.5.5]fenestrane (Fenestrindane) Core Merged with Two Hexa-peri-hexabenzocoronene UnitsCorrection to Regiocontrolled Synthesis and Optical Resolution of Mono-, Di-, and Trisubstituted Tribenzotriquinacene Derivatives: Key Building Blocks for Further Assembly into Molecular Squares and CubesA Phosphine-Catalyzed Regioselective [3+2] Cycloaddition of Ethyl 5,5-Diarylpenta-2,3,4-trienoate with Aromatic Aldehydes and α,β-Unsaturated Carbonyl CompoundsSupramolecular Chemistry of Click Linear Oligo- and Poly-(amide-triazole)sC3-Symmetrical Tribenzotriquinacene Derivatives: Optical Resolution through Cryptophane Synthesis and Supramolecular Self-Assembly into NanotubesFrom Nongelating to Gelating: Synthesis and Structural Self-Assembling Property Relationships of a Homologous Series of Oligo(amide-triazole)sSynthesis and Thermoreversible Gelation Properties of Main-Chain Poly(pyridine-2,6-dicarboxamide-triazole)sVersatile Synthesis of Amphiphilic Oligo(Aliphatic-Glycerol) Layer-Block Dendrons with Different Hydrophilic-Lipophilic Balance ValuesHead-to-Tail Dimerization and Organogelating Properties of Click PeptidomimeticsEnhanced gelation property due to intra-molecular hydrogen bonding in a new series of bis(amino acid)-functionalized pyridine-2,6-dicarboxamide organogelatorsImproving the gelation properties of 3,5-diaminobenzoate-based organogelators in aromatic solvents with additional aromatic-containing pendantsStereocontrol in organic synthesis using silicon-containing compounds. A synthesis of the (±)-Prelog–Djerassi lactoneAn Efficient and Convenient Synthesis of Chain Lengthened Homologs of the Fungicide MetalaxylIsolation from atelia herbert-smithii pittier (sophoreae, leguminosae) and x-ray structure of cis-1-amino-3-hydroxymethyl-cyclobutane-1-carboxylic acid, an achiral non-protein amino acidSynthesis of 2s, 4s, 5s -dihydroxypipecolic acid and bulgecinine [2s,4s,5r-4-hydroxy-5- (hydroxymethyl)proline] from d-glucuronolactone, a strategy for the synthesis of 2s,4s-4-hydroxy-α-amino acidsThe synthesis of polyhydroxylated amino acids from glucuronolactone: enantiospecific syntheses of 2s, 3r, 4r, 5s-trihydroxypipecolic acid, 2r, 3r, 4r, 5s-trihydroxypipecolic acid and 2r, 3r, 4r-dihydroxyprolineDiastereoselective Aldol Addition Using Boron Trichloride or Alkoxydichloroborane
P50
Q27683531-20070F04-2D19-47E1-8DDD-865C0A64107EQ33719542-A2170A28-E78E-4E88-8E40-684F1DC718CCQ33749869-F6AFCCC9-2BD2-483F-A50B-4CF68EAF16E5Q34071874-294890B6-85D8-45FE-90BB-CCAD567B2504Q35538731-3587E24A-CD92-4506-B859-2661298589CDQ43091165-CFC67E22-45EE-434E-90DC-C2851F38AF82Q45992847-59E17A03-39CC-4E9B-B1EE-71B4948C63B4Q47176103-30F7E9CD-B992-488E-9551-5521785AD99CQ47184097-E7813B1F-FB8A-4077-97EF-CAF78F0F82D4Q47371117-C0AF798D-E138-4A21-AEAA-67EA3DD1D897Q48171113-3CF0C134-E305-48F1-B8E2-7B69B99A921BQ48241673-A8B87812-9AC6-499F-B519-1C7DD33E9748Q48306825-DBC42712-3D47-48CF-9AB5-4137C9B85222Q50484764-E5A655B3-2570-4670-9672-85F3C1FCA979Q51012590-38BDE6AC-18C7-4701-BC95-2153C4A3145AQ51472670-4B43C653-87F9-46B5-8D9F-9AD771E1D66CQ51578780-56CA9B94-47ED-4E83-94D4-E1EFFFD871A6Q52648612-5C0BD60C-DDD2-4833-999A-036DAC496604Q52677674-5624CD67-D403-42E0-AA74-9F9EAA831259Q57180296-A862EC2C-AE6B-4CB3-9C9B-9D9EF4A60847Q58324594-6CE6A09F-5423-44C5-91F3-17990AD04FABQ59439777-47302C94-7CFD-4187-B5F6-8F685242B22DQ59439779-6BDE5AA4-FCD9-4627-B16C-751AD33EA97CQ59439782-72AB7E82-EA14-4D9E-935D-2F655579C245Q59439786-E8FF081B-F4CF-422E-BFDA-7E4B4CF8D71DQ59439788-7E4094C9-B040-47A4-8BAB-E66918683A96Q59439790-030C6CCA-3A9D-4651-B5F3-B7F92B8A2EF3Q59439791-3E4D2DB2-C38C-48CB-8024-E94E2778EEB0Q59439793-01739D7F-162F-439D-B6C2-B5B3B9E87F26Q59439796-E2855D3D-D34E-4E5A-82DF-E9ED6FE3C886Q59439798-8521A629-8C8F-43BF-B433-D4F6D2CE4E5FQ59439800-BC45FAB3-3AA5-41F9-AD79-3BED2D9EA774Q59439803-D48D6BF5-9571-49F4-8DEA-573FFE74A946Q59439805-D435ABCB-97A1-45B7-B55A-CA9213668CD1Q59439808-CDB9B789-3602-4089-8A0E-AFC4861DD29CQ59439810-4FC16D06-2B88-43D4-98AB-17DDEF40A255Q59439812-4CA085C8-9176-477E-9554-2E570510C44BQ59439814-814565B8-249D-400D-AA8E-E21D409E8F34Q59439815-02B271D8-87A4-409D-B66B-396FB64CD6BFQ59439818-D58291CD-07AC-4E68-AE70-94C99FBF1E08
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Hak-Fun Chow
@ast
Hak-Fun Chow
@en
Hak-Fun Chow
@es
Hak-Fun Chow
@nl
Hak-Fun Chow
@sl
type
label
Hak-Fun Chow
@ast
Hak-Fun Chow
@en
Hak-Fun Chow
@es
Hak-Fun Chow
@nl
Hak-Fun Chow
@sl
prefLabel
Hak-Fun Chow
@ast
Hak-Fun Chow
@en
Hak-Fun Chow
@es
Hak-Fun Chow
@nl
Hak-Fun Chow
@sl
P1053
A-9925-2008
P106
P21
P31
P3829
P496
0000-0002-7621-0851