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
Capture of benzotriazole-based Mannich electrophiles by CH-acidic compounds
Jean-Christophe Monbaliu,Jean-Christophe Monbaliu,Lucas K. Beagle,Finn K. Hansen,Finn K. Hansen,Christian V. Stevens,Ciaran B. McArdle,Alan R. Katritzky,Alan R. Katritzky +8 more
TL;DR: The Mannich-type capture reaction of aminoalkylbenzotriazoles by CH acidic compounds is documented in this article, where the pKa of the benzotrizole counteranion is key to the success of such reactions, whereas global electrophilicity of the reactive iminium moiety is secondary.
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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 discussed by the authors.
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Double Nucleophilic 1,2-Addition of Silylated Dialkyl Phosphites to 4-Phosphono-1-aza-1,3-dienes: Synthesis of γ-Phosphono-α-aminobisphosphonates.
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Synthesis of 1-Phosphono-2-aza-1,3-dienes and Their Conversion into 1-Vinyl-2-phosphonoaziridines.
TL;DR: In this paper, 1-Phosphono-2-aza-1, 3-dienes were formed by 1, 4-dehydro-chlorination of the corresponding α-chloroimines and reacted with diazomethane to give 1-vinyl-2phosphonoaziridines.
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Synthesis of 1,1‐Bisphosphono‐2‐aza‐1,3‐dienes, a New Class of Electron‐Deficient Azadienes.
TL;DR: In this article, 1,1-Bisphosphono-2-aza-1,3-dienes are formed by 1,4-dehydrohalogenation of the corresponding N-(bisphosphonomethyl)-α-haloimines in moderate to good yields.