Karl Gademann

Cette personne n’est plus à l’EPFL

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Publications associées (49)

Total Synthesis of Complex Cyanobacterial Alkaloids Without Using Protecting Groups

Simone Bonazzi, Karl Gademann

Wiley-VCH Verlag GmbH2007

Total Synthesis, Configuration, and Biological Evaluation of Anguinomycin C

Simone Bonazzi, Karl Gademann, Ivo Zemp

Immunofluorescence assays indicate that anguinomycin C is a potent inhibitor of protein export from the nucleus. Key features in the total synthesis of this antitumor natural product include a Cr-catalyzed enantioselective hetero-Diels– Alder reaction, a N ...

Wiley-VCH Verlag GmbH2007

Combining Devices and Drugs by Synthetic Natural Product Hybrids

Simone Bonazzi, Karl Gademann, Jean-Yves Wach

2007

Novel screening protocol for wet chemical surface functionalization

Karl Gademann

2007

Cyanobacterial Natural Products for the Inhibition of Biofilm Formation and Biofouling

Karl Gademann

Biofouling is defined by the non-specific attachment of biological material (proteins, carbohydrates, prokaryotic cells and higher organisms) to surfaces upon their exposure to any biological fluid. Biofouling is a serious problem in many areas ranging fro ...

2007

Novel screening protocol for universal applicable adhesive molecules

Karl Gademann

2007

Natural Product Hybrids

Karl Gademann

This review highlights several classes of natural product hybrids. First, structural hybrids emanating from different biosynthetic pathways exemplified by the polyketide peptide alkaloid anachelin are discussed. Another class is the so-called functional hy ...

2006

Heterocyclic compounds and their use as antifouling agents

Karl Gademann

The present invention relates to a nostocarboline compound and its use as biocidal agent. ...

2005

Catechol functionalized polymers and method for preparing them

Karl Gademann

Described are compounds that are capable of forming adlayers, said compounds comprising at least one headgroup A, an optional linker B, a polymer C, a terminal group D and an optionally present crosslinking group R, wherein the headgroup A is a compound of ...

2005

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