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Juraj Velcicky

Showing results (1-10 of 27) with videos related to

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Organic Letters|February 15, 2002
An efficient organometallic approach to new carbocyclic nucleoside analoguesJuraj Velcicky, Johann Lex, Hans-Günther Schmalz
Journal of the American Chemical Society|April 21, 2011
Palladium-catalyzed cyanomethylation of aryl halides through domino Suzuki coupling-isoxazole fragmentationJuraj Velcicky, Arne Soicke, Roland Steiner, et al.
European Journal of Pharmacology|April 2, 2019
Pharmacological inhibition of GPR4 remediates intestinal inflammation in a mouse colitis modelEdward J Sanderlin, Mona Marie, Juraj Velcicky, et al.
Journal of the American Chemical Society|August 10, 2006
Total synthesis of (-)- and ent-(+)-vindoline and related alkaloidsHayato Ishikawa, Gregory I Elliott, Juraj Velcicky, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|September 17, 2004
Transition-metal-mediated synthesis of novel carbocyclic nucleoside analogues with antitumoral activityJuraj Velcicky, Andreas Lanver, Johann Lex, et al.
Organic Letters|September 24, 2005
Total synthesis of (-)- and ent-(+)-vindolineYounggi Choi, Hayato Ishikawa, Juraj Velcicky, et al.
Iscience|February 15, 2020
The Proton-Sensing GPR4 Receptor Regulates Paracellular Gap Formation and Permeability of Vascular Endothelial CellsElizabeth A Krewson, Edward J Sanderlin, Mona A Marie, et al.
ACS Medicinal Chemistry Letters|April 20, 2018
Modulating ADME Properties by Fluorination: MK2 Inhibitors with Improved Oral ExposureJuraj Velcicky, Achim Schlapbach, Richard Heng, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|August 13, 2013
Nucleoside analogues with a 1,3-diene-Fe(CO)3 substructure: stereoselective synthesis, configurational assignment, and apoptosis-inducing activityChristoph Hirschhäuser, Juraj Velcicky, Daniel Schlawe, et al.
Bioorganic & Medicinal Chemistry Letters|January 12, 2010
Novel 3-aminopyrazole inhibitors of MK-2 discovered by scaffold hopping strategyJuraj Velcicky, Roland Feifel, Stuart Hawtin, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Organic Letters|February 15, 2002
An efficient organometallic approach to new carbocyclic nucleoside analoguesJuraj Velcicky, Johann Lex, Hans-Günther Schmalz
Journal of the American Chemical Society|April 21, 2011
Palladium-catalyzed cyanomethylation of aryl halides through domino Suzuki coupling-isoxazole fragmentationJuraj Velcicky, Arne Soicke, Roland Steiner, et al.
European Journal of Pharmacology|April 2, 2019
Pharmacological inhibition of GPR4 remediates intestinal inflammation in a mouse colitis modelEdward J Sanderlin, Mona Marie, Juraj Velcicky, et al.
Journal of the American Chemical Society|August 10, 2006
Total synthesis of (-)- and ent-(+)-vindoline and related alkaloidsHayato Ishikawa, Gregory I Elliott, Juraj Velcicky, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|September 17, 2004
Transition-metal-mediated synthesis of novel carbocyclic nucleoside analogues with antitumoral activityJuraj Velcicky, Andreas Lanver, Johann Lex, et al.
Organic Letters|September 24, 2005
Total synthesis of (-)- and ent-(+)-vindolineYounggi Choi, Hayato Ishikawa, Juraj Velcicky, et al.
Iscience|February 15, 2020
The Proton-Sensing GPR4 Receptor Regulates Paracellular Gap Formation and Permeability of Vascular Endothelial CellsElizabeth A Krewson, Edward J Sanderlin, Mona A Marie, et al.
ACS Medicinal Chemistry Letters|April 20, 2018
Modulating ADME Properties by Fluorination: MK2 Inhibitors with Improved Oral ExposureJuraj Velcicky, Achim Schlapbach, Richard Heng, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|August 13, 2013
Nucleoside analogues with a 1,3-diene-Fe(CO)3 substructure: stereoselective synthesis, configurational assignment, and apoptosis-inducing activityChristoph Hirschhäuser, Juraj Velcicky, Daniel Schlawe, et al.
Bioorganic & Medicinal Chemistry Letters|January 12, 2010
Novel 3-aminopyrazole inhibitors of MK-2 discovered by scaffold hopping strategyJuraj Velcicky, Roland Feifel, Stuart Hawtin, et al.
Pageof 3