All journal publications (1963-2013)
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- 2005
Selective cross-metathesis of C-allyl-glycosides,
Journal of Carbohydrate Chemistry, vol. 24, no. 4-6, pp. 335-351.
A modular strategy toward the synthesis of heparin-like oligosaccharides using monomeric building blocks in a sequential glycosylation strategy,
Journal of the American Chemical Society, vol. 127, no. 11, pp. 3767-3773.
1,3-Dimethyllumazine derivatives from Limnatis nilotica,
Journal of Natural Products, vol. 68, no. 6, pp. 938-941.
Synthesis of functionalized heterocycles via a tandem Staudinger/aza-Wittig/Ugi multicomponent reaction,
Tetrahedron-Asymmetry, vol. 16, no. 1, pp. 177-185.
Solid-phase synthesis of peptide-platinum complexes using platinum-chelating building blocks derived from amino acids,
New Journal of Chemistry, vol. 29, no. 1, pp. 220-225. DOI
- 2004
A tandem ring-closing metathesis cleavable linker system for solid-phase oligosaccharide synthesis,
Synlett, no. 12, pp. 2155-2158.
A practical synthesis of gramicidin S and sugar amino acid containing analogues,
Journal of Organic Chemistry, vol. 69, no. 23, pp. 7851-7859.
Synthesis and in vitro evaluation of PNA-peptide-DETA conjugates as potential cell penetrating artificial ribonucleases,
Bioconjugate Chemistry, vol. 15, no. 3, pp. 576-582.
Glycosylation of cyclitols: Synthesis of neamine-type aminoglycosides,
European Journal of Organic Chemistry, no. 11, pp. 2404-2410.
Ring-closing alkyne metathesis mediated synthesis of cyclic beta-turn mimetics,
Tetrahedron Letters, vol. 45, no. 22, pp. 4379-4382.
Synthesis of orthogonally protected 2-deoxystreptamine stereoisomers,
Tetrahedron, vol. 60, no. 12, pp. 2813-2822.
Design and synthesis of 2-acetamidomethyl derivatives of isofagomine as potential inhibitors of human lysosomal beta-hexosaminidases,
Bioorganic & Medicinal Chemistry, vol. 12, no. 5, pp. 891-902.
Effect of bulky lesions on DNA - Solution structure of a DNA duplex containing a cholesterol adduct,
Journal of Biological Chemistry, vol. 279, no. 23, pp. 24552-24560.
Thioglycuronides: Synthesis and application in the assembly of acidic oligosaccharides,
Organic Letters, vol. 6, no. 13, pp. 2165-2168.
Design, synthesis, and evaluation of sugar amino acid based inhibitors of protein prenyl transferases PFT and PGGT-1,
Journal of Medicinal Chemistry, vol. 47, no. 16, pp. 3920-3923.
Structure of an anti-Lewis X fab fragment in complex with its Lewis X antigen,
Structure, vol. 12, no. 7, pp. 1227-1236.
Surface plasmon resonance evaluation of various aminoglycoside-RNA hairpin interactions reveals low degree of selectivity,
Chembiochem, vol. 5, no. 7, pp. 937-942.
Chemoselective glycosylations using sulfonium triflate activator systems,
Tetrahedron, vol. 60, no. 5, pp. 1057-1064.
Synthesis of peptide-PNA-peptide conjugates by semi-solid-phase chemical ligation combined with deactivation/capture of excess reactants,
European Journal of Organic Chemistry, no. 4, pp. 850-857.
Chemically synthesized protein as tumour-specific vaccine: immunogenicity and efficacy of synthetic HPV16 E7 in the TC-1 mouse tumour model,
Vaccine, vol. 23, no. 3, pp. 305-311.
Effective, high-yielding, and stereospecific total synthesis of D-erythro-(2R,3S)-sphingosine from D-ribo-(2S,3S,4R)-phytosphingosine,
Journal of Organic Chemistry, vol. 69, no. 17, pp. 5699-5704.
The beta-glucuronyl-based prodrug strategy allows for its application on beta-glucuronyl-platinum conjugates,
Bioorganic & Medicinal Chemistry Letters, vol. 14, no. 16, pp. 4273-4276.
Novel reversed chain modified oligopeptides via sequential alpha-N-mitsunobu condensation of a functionalized C-glycoside,
Chemistry Letters, vol. 33, no. 4, pp. 468-469.
An expeditious route towards pyranopyran sugar amino acids,
Synlett, no. 5, pp. 904-906.
Parallel solid phase synthesis of tricomponent bisubstrate analogues as potential fucosyltransferase inhibitors,
Synlett, no. 5, pp. 773-778.


