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Chemical Communications (Cambridge, England)|April 23, 2005
Efficient batch and continuous flow Suzuki cross-coupling reactions under mild conditions, catalysed by polyurea-encapsulated palladium (II) acetate and tetra-n-butylammonium saltsConnie K Y Lee, Andrew B Holmes, Steven V Ley, et al.European Journal of Medicinal Chemistry|July 22, 2015
Design, synthesis and evaluation of semi-synthetic triazole-containing caffeic acid analogues as 5-lipoxygenase inhibitorsDaniela De Lucia, Oscar Méndez Lucio, Biagia Musio, et al.Organic Letters|September 26, 2008
Enantiopure 2-substituted glyceraldehyde derivatives by aza-Claisen rearrangement or C-alkylation of enaminesKaty L Bridgwood, C Christoph Tzschucke, Matthew O'Brien, et al.The Journal of Biological Chemistry|February 18, 2011
Allosteric modulation of hormone release from thyroxine and corticosteroid-binding globulinsXiaoqiang Qi, François Loiseau, Wee Lee Chan, et al.Journal of Medicinal Chemistry|April 28, 2016
Identification and Development of 2,3-Dihydropyrrolo[1,2-a]quinazolin-5(1H)-one Inhibitors Targeting Bromodomains within the Switch/Sucrose Nonfermenting ComplexCharlotte L Sutherell, Cynthia Tallant, Octovia P Monteiro, et al.ACS Medicinal Chemistry Letters|June 6, 2014
Flow Synthesis and Biological Studies of an Analgesic Adamantane Derivative That Inhibits P2X7-Evoked Glutamate ReleaseClaudio Battilocchio, Lucie Guetzoyan, Chiara Cervetto, et al.ACS Medicinal Chemistry Letters|March 28, 2015
Design, Synthesis, and Evaluation of Tetrasubstituted Pyridines as Potent 5-HT2C Receptor AgonistsGuy Rouquet, Dianna E Moore, Malcolm Spain, et al.Chemistry & Biology|November 12, 2013
Design, synthesis, and biological evaluation of an allosteric inhibitor of HSET that targets cancer cells with supernumerary centrosomesCiorsdaidh A Watts, Frances M Richards, Andreas Bender, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|March 18, 2011
Total synthesis of chloptosin: a dimeric cyclohexapeptideAlexander J Oelke, Francesca Antonietti, Leonardo Bertone, et al.ACS Medicinal Chemistry Letters|June 6, 2014
A-ring dihalogenation increases the cellular activity of combretastatin-templated tetrazolesThomas M Beale, Daniel M Allwood, Andreas Bender, et al.Pageof 24