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- Publications
- Influence
Selective enrichment of azide-containing peptides from complex mixtures.
- M. A. Nessen, G. Kramer, +8 authors C. D. de Koster
- Chemistry, Medicine
- Journal of proteome research
- 26 May 2009
A general method is described to sequester peptides containing azides from complex peptide mixtures, aimed at facilitating mass spectrometric analysis to study different aspects of proteome dynamics.… Expand
Conformationally homogeneous heterocyclic pseudotetrapeptides as three-dimensional scaffolds for rational drug design: receptor-selective somatostatin analogues.
- John M. Beierle, W. Horne, J. V. van Maarseveen, B. Waser, J. Reubi, M. Ghadiri
- Chemistry, Medicine
- Angewandte Chemie
- 15 June 2009
A would-be amide: A 1,4-disubstituted 1,2,3-triazole was used as a surrogate for a trans amide bond to create a library of 16 diastereomeric pseudotetrapeptides as beta-turn mimetics. High-resolution… Expand
An Aptly Positioned Azido Group in the Spacer of a Protein Cross‐Linker for Facile Mapping of Lysines in Close Proximity
- P. Kasper, Jaap Willem Back, +7 authors L. de Jong
- Chemistry, Medicine
- Chembiochem : a European journal of chemical…
- 23 July 2007
Cross‐links between amino acid residues in close proximity can provide distance constraints for the validation of models of the 3D structure proteins. The mapping of cross‐links by the identification… Expand
Organocatalytic enantioselective Pictet-Spengler approach to biologically relevant 1-benzyl-1,2,3,4-tetrahydroisoquinoline alkaloids.
- Andrea Ruiz-Olalla, M. A. Würdemann, M. Wanner, S. Ingemann, J. V. van Maarseveen, H. Hiemstra
- Chemistry, Medicine
- The Journal of organic chemistry
- 7 May 2015
A general procedure for the synthesis of 1-benzyl-1,2,3,4-tetrahydroisoquinolines was developed, based on organocatalytic, regio- and enantioselective Pictet-Spengler reactions (86-92% ee) of… Expand
Click chemistry as a route to cyclic tetrapeptide analogues: synthesis of cyclo-[Pro-Val-psi(triazole)-Pro-Tyr].
- Victoria D. Bock, R. Perciaccante, T. P. Jansen, H. Hiemstra, J. V. van Maarseveen
- Chemistry, Medicine
- Organic letters
- 8 February 2006
Despite the plethora of techniques to cyclize small peptides, a synthesis of cyclo-[(L)Pro-(L)Tyr-(L)Pro-(L)Val], a potent tyrosinase inhibitor, remains elusive because of the unfavorable transition… Expand
Efficient route to C2 symmetric heterocyclic backbone modified cyclic peptides.
- J. V. van Maarseveen, W. Horne, M. Ghadiri
- Chemistry, Biology
- Organic letters
- 31 August 2005
[reaction: see text] A tandem dimerization-macrocyclization approach using 1,3-dipolar azide-alkyne cycloaddition reactions has been employed in the facile and convergent solution phase syntheses of… Expand
Enantioselective copper-catalysed propargylic substitution: synthetic scope study and application in formal total syntheses of (+)-anisomycin and (-)-cytoxazone.
- R. Detz, Z. Abiri, Remi le Griel, H. Hiemstra, J. V. van Maarseveen
- Chemistry, Medicine
- Chemistry
- 16 May 2011
A copper catalyst with a chiral pyridine-2,6-bisoxazoline (pybox) ligand was used to convert a variety of propargylic esters with different side chains (R=Ar, Bn, alkyl) into their amine counterparts… Expand
Folding dynamics of the Trp-cage miniprotein: evidence for a native-like intermediate from combined time-resolved vibrational spectroscopy and molecular dynamics simulations.
- H. Meuzelaar, Kristen A. Marino, +7 authors S. Woutersen
- Chemistry, Medicine
- The journal of physical chemistry. B
- 19 September 2013
Trp-cage is a synthetic 20-residue miniprotein which folds rapidly and spontaneously to a well-defined globular structure more typical of larger proteins. Due to its small size and fast folding, it… Expand
A mixed ladderane/n-alkyl glycerol diether membrane lipid in an anaerobic ammonium-oxidizing bacterium.
- J. S. Sinninghe Damsté, W. Rijpstra, +4 authors J. V. van Maarseveen
- Chemistry, Medicine
- Chemical communications
- 12 November 2004
A novel glycerol diether containing ladderane and tetradecyl moieties has been identified in an anaerobic ammonium-oxidizing bacterium by GC/MS and high-field NMR spectroscopy.
Total syntheses of mitragynine, paynantheine and speciogynine via an enantioselective thiourea-catalysed Pictet-Spengler reaction.
- Isabel P Kerschgens, E. Claveau, M. Wanner, S. Ingemann, J. V. van Maarseveen, H. Hiemstra
- Chemistry, Medicine
- Chemical communications
- 21 November 2012
The pharmacologically interesting indole alkaloids (-)-mitragynine, (+)-paynantheine and (+)-speciogynine were synthesised in nine steps from 4-methoxytryptamine by a route featuring (i) an… Expand