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Home page > Publications > Chemical Biology

2016

by Nathalie Ollivier - published on , updated on

Accelerating chemoselective peptide bond formation using bis(2-selenylethyl)amido peptide selenoester surrogates Laurent Raibaut, Marine Cargoët, Nathalie Ollivier, Yun Min Chang, Hervé Drobecq, Emmanuelle Boll, Rémi Desmet, Jean-Christophe M. Monbaliu and Oleg Melnyk, Chem. Sci. , 2016, 7, 2657-2665. DOI: 10.1039/C5SC03459K

 

Kinetically controlled chemoselective cyclization simplifies the access to cyclic and branched peptides Boll, E., Drobecq, H., Lissy, E., Cantrelle, F.-X., Melnyk, O. Org. Lett. 2016, 18, 3842-3845. DOI: 10.1021/acs.orglett.6b01847.

 

Cysteine 52 is the Achilles’ heel of SUMO-1 Drobecq, H. ; Boll, E. ; Sénéchal, M. ; Desmet, R. ; Saliou, J. M. ; Lacapère, J.-J. ; Mougel, A. ; Vicogne, V. ; Melnyk, O. Bioconjugate Chem. 2016, 27 1540–1546. DOI: 10.1021/acs.bioconjchem.6b00211

 

Insight into the SEA amide thioester equilibrium. Application to the synthesis of thioesters at neutral pH Pira, S. L., El Mahdi, O., Raibaut, L., Drobecq, H., Dheur, J., Boll, E., and Melnyk, O. Org. Biomol. Chem. 2016, 14, 7211-7216. DOI : 10.1039/C6OB01079B

 

Total chemical synthesis of SUMO proteins Melnyk, O.; Vicogne, J. Tetrahedron Letters 2016 , 57, 4319-4324. DOI: 10.1016/j.tetlet.2016.08.035