C
Christian V. Stevens
Researcher at Ghent University
Publications - 483
Citations - 14254
Christian V. Stevens is an academic researcher from Ghent University. The author has contributed to research in topics: Catalysis & Ring (chemistry). The author has an hindex of 45, co-authored 467 publications receiving 11742 citations. Previous affiliations of Christian V. Stevens include Katholieke Universiteit Leuven & University of Minnesota.
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Journal ArticleDOI
Synthesis and self-assembly of aminyl and alkynyl substituted sophorolipids
Abdoul Aziz Ba,Jonas Everaert,Alexandre Poirier,Patrick Le Griel,Wim Soetaert,Sophie Roelants,Daniel Hermida-Merino,Christian V. Stevens,Niki Baccile +8 more
TL;DR: In this paper, the authors developed a new generation of pH-responsive, positively charged, sophorolipids with an amine (−NH2) or terminal alkyne (−CCH) end-group analogues.
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Single-Molecule Lamellar Hydrogels from Bolaform Microbial Glucolipids
Ghazi Ben Messaoud,Patrick Le Griel,Sylvain Prévost,Daniel Hermida-Merino,Wim Soetaert,Wim Soetaert,Sophie Roelants,Sophie Roelants,Christian V. Stevens,Niki Baccile +9 more
TL;DR: In this article, a new class of lipid lamellar hydrogels composed of one single bolaform glycosylated lipid obtained by fermentation is reported. And the authors show that ionic strength is not only necessary, as one could expect, to control the interactions in the laminar phase but, most importantly, it directly controls the elastic properties of the gels.
Journal Article
Fungicidal effect of chitosan derivatives containing an N-alkyl group on grey mould Botryti77s cinerea and rice leaf blast Pyricularia grisea.
Entsar I. Rabea,Mohamed E. I. Badawy,Walter Steurbaut,Tina Rogge,Christian V. Stevens,Guy Smagghe,Monica Höfte +6 more
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Exploiting the regioselectivity of pyroglutamate alkylations for the synthesis of 6-azabicyclo[3.2.1]octanes and 4-azabicyclo[3.3.0]octanes
TL;DR: In this paper, the reactivity of 6-azabicyclo[3.2.1] octanes or 4-azabinicyclos[3,3.3.0]octanes was shown to be a function of the N protecting group of pyroglutamates.
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Synthesis of 2,5-difunctionalised-3,3-dimethylpiperidines via ω-halogenated imines
TL;DR: In this article, 2,5-Difunctionalised 3,3-dimethylpiperidines were prepared by addition of nucleophiles to piperideinium salts, formed by electrophile-induced cyclisation of γ,δ-unsaturated imines with N-bromosuccinimide in alcoholic medium.