Search Results - "Smout, Veerle"

C-2 Arylation of Piperidines through Directed Transition-Metal-Catalyzed sp3 CH Activation by Prokopcová, Hana, Bergman, Sheba D., Aelvoet, Karel, Smout, Veerle, Herrebout, Wouter, Van der Veken, Benjamin, Meerpoel, Lieven, Maes, Bert U. W.

“…All you need is an open vial! The direct α arylation of cyclic alkylamines (see scheme) requires an open vial, as the hydrogen atom involved in the…”
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Ruthenium-Catalyzed α-(Hetero)Arylation of Saturated Cyclic Amines: Reaction Scope and Mechanism by Peschiulli, Aldo, Smout, Veerle, Storr, Thomas E., Mitchell, Emily A., Eliáš, Zdeněk, Herrebout, Wouter, Berthelot, Didier, Meerpoel, Lieven, Maes, Bert U. W.

“…Transition‐metal‐catalyzed sp3 CH activation has emerged as a powerful approach to functionalize saturated cyclic amines. Our group recently disclosed a…”
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Removal of the Pyridine Directing Group from α‑Substituted N‑(Pyridin-2-yl)piperidines Obtained via Directed Ru-Catalyzed sp3 C–H Functionalization by Smout, Veerle, Peschiulli, Aldo, Verbeeck, Stefan, Mitchell, Emily A, Herrebout, Wouter, Bultinck, Patrick, Vande Velde, Christophe M. L, Berthelot, Didier, Meerpoel, Lieven, Maes, Bert U. W

“…Two strategies, “hydrogenation–hydride reduction” and “quaternization–hydride reduction”, are reported that make use of mild reaction conditions (room…”
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Ruthenium-Catalyzed [alpha]-(Hetero)Arylation of Saturated Cyclic Amines: Reaction Scope and Mechanism by Peschiulli, Aldo, Smout, Veerle, Storr, Thomas E, Mitchell, Emily A, Eliás, Zdenk, Herrebout, Wouter, Berthelot, Didier, Meerpoel, Lieven, Maes, Bert U. W

“…Transition-metal-catalyzed sp3 CH activation has emerged as a powerful approach to functionalize saturated cyclic amines. Our group recently disclosed a direct…”
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Highly efficient one-pot synthesis of D-ring chloro-substituted neocryptolepines via a condensation—Pd-catalyzed intramolecular direct arylation strategy by Hostyn, Steven, Tehrani, Kourosch Abbaspour, Lemière, Filip, Smout, Veerle, Maes, Bert U.W.

“…D-ring chloro-substituted neocryptolepines have been synthesized in excellent yield starting from 3-bromo-2-chloro-1-methylquinolinium triflate via a one-pot…”
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Removal of the Pyridine Directing Group from α-Substituted N -(Pyridin-2-yl)piperidines Obtained via Directed Ru-Catalyzed sp 3 C–H Functionalization by Smout, Veerle, Peschiulli, Aldo, Verbeeck, Stefan, Mitchell, Emily A., Herrebout, Wouter, Bultinck, Patrick, Vande Velde, Christophe M. L., Berthelot, Didier, Meerpoel, Lieven, Maes, Bert U. W.

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C-2 Arylation of Piperidines through Directed Transition-Metal-Catalyzed sp3 CH Activation by Prokopcova, Hana, Bergman, Sheba D, Aelvoet, Karel, Smout, Veerle, Herrebout, Wouter, VanderVeken, Benjamin, Meerpoel, Lieven, Maes, Bert U W

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C‐2 Arylation of Piperidines through Directed Transition‐Metal‐Catalyzed sp 3 CH Activation by Prokopcová, Hana, Bergman, Sheba D., Aelvoet, Karel, Smout, Veerle, Herrebout, Wouter, Van der Veken, Benjamin, Meerpoel, Lieven, Maes, Bert U. W.

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