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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Fundamental Study on the Salt Tolerance of Oregano Essential Oil-in-Water Nanoemulsions Containing Tween 80
TL;DR: The emulsion stability was found to be strongly correlated with the lipid phase composition and the type of salts, and it is hypothesized that a combination of Ostwald ripening and coalescence due to an IFT increase and dehydration was responsible for the instability of the emulsions containing the more polar oregano EO and carvacrol in the presence of salt.
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Synthesis of substituted cyclopropylphosphonates by Michael Induced Ring Closure (MIRC) reactions
Christian V. Stevens,Gino Van Heecke,Carmen Barbero,Krystyna Patora,Norbert De Kimpe,R. Verhé +5 more
TL;DR: A variety of cyclopropylphosphonates were prepared in moderate to good yields by Michael Induced Ring Closure of trialkyl phosphites with the corresponding β-bromoalkylidene cyanoacetates and malonates as mentioned in this paper.
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Exploration of the SAR of anti-invasive chalcones: synthesis and biological evaluation of conformationally restricted analogues.
Bart Roman,Tine De Ryck,Laura Dierickx,Barbara Vanhoecke,Alan R. Katritzky,Alan R. Katritzky,Marc Bracke,Christian V. Stevens +7 more
TL;DR: In vitro anti-invasive activity data point towards an active conformation for chalcones more resembling their s-trans geometry than the s-cis counterpart.
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Synthesis of 1-amino-2,2-dialkylcyclopropanecarboxylic acids from β-chloroaldimines
TL;DR: In this article, a variety of hydrogen cyanide adducts of β-chloroaldimines using acetone cyanohydrin were prepared, and the reactive behavior of these α-amino-γ-chloronitriles towards bases was investigated with the aim to generate 1-aminocyclopropanecarbonitrile, which are precursors for the potentially plant growth regulating 1-AMINOCOPPARANecarboxylic acids.
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Gold superacid-catalyzed preparation of benzo[c]thiophenes
TL;DR: A three-step synthesis of benzo[c]thiophenes is presented in which the key transformation is the gold-catalyzed 5-exo-dig migratory cycloisomerization of a diallyl thioacetal.