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774Michal Sobkowski.
Chemistry and stereochemistry of internucleotide bond formation by the H-phosphonate method, New J. Chem., 2010, 34, 854. Stewart A. Forsyth, Ute Fröhlich, Peter Goodrich, H. Q. Nimal Gunaratne, Christopher Hardacre, Angela McKeown and Kenneth R. Seddon.
Functionalised ionic liquids: synthesis of ionic liquids with tethered basic groups and their use in Heck and Knoevenagel reactions, New J. Chem., 2010, 34, 723. André Beyer, Adelheid Godt, Ihsan Amin, Christoph T. Nottbohm, Christian Schmidt, Jinkai Zhao and Armin Gölzhäuser.
Fully cross-linked and chemically patterned self-assembled monolayers, Phys. Chem. Chem. Phys., 2008, 10, 7233. Jörn Wolf, Valeska Dombos, Bettina Appel and Sabine Müller.
Synthesis of guanosine 5′-conjugates and their use as initiator molecules for transcription priming, Org. Biomol. Chem., 2008, 6, 899. Gaston Lavén, Marcin Kalek, Martina Jezowska and Jacek Stawinski.
Preparation of benzylphosphonates via a palladium(0)-catalyzed cross-coupling of H-phosphonatediesters with benzyl halides. Synthetic and mechanistic studies, New J. Chem., 2010, 34, 967. Hsuan-Yi HsiaoThese authors contributed equally to this work., Mu-Lin Chen, Huan-Ting Wu, Li-De Huang, Wei-Ting Chien, Ching-Ching Yu, Fan-Dan Jan, Sk Sahabuddin, Tsung-Che Chang and Chun-Cheng Lin.
Fabrication of carbohydrate microarrays through boronate formation, Chem. Commun., 2011, 47, 1187. Giovanni Di Fabio, Jennifer D'Onofrio, Mariateresa Chiapparelli, Bart Hoorelbeke, Daniela Montesarchio, Jan Balzarini and Lorenzo De Napoli.
Discovery of novel anti-HIV active G-quadruplex-forming oligonucleotides, Chem. Commun., 2011, 47, 2363. Premaladha Poddutoori, Dick T. Co, Amanda P. S. Samuel, Chul Hoon Kim, Michael T. Vagnini and Michael R. Wasielewski.
Photoinitiated multistep charge separation in ferrocene–zinc porphyrin–diiron hydrogenase model complex triads, Energy Environ. Sci., 2011, 4, 2441. Ilona B. Bruinsma, Anna Karawajczyk, Gijs Schaftenaar, Robert M. W. de Waal, Marcel M. Verbeek and Floris L. van Delft.
A rational design to create hybrid β-sheet breaker peptides to inhibit aggregation and toxicity of amyloid-β, Med. Chem. Commun., 2011, 2, 60.