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Organic Letters|May 28, 2011
Stereoselective synthesis of deuterated β-cyclohexenylserine, a biosynthetic intermediate of the salinosporamidesJan Deska, Saskia Hähn, Uli KazmaierCurrent Organic Synthesis|January 14, 2021
Synthesis of New Cyclopeptide Analogues of the MiuraenamidesSarah Kappler, Andreas Siebert, Uli KazmaierThe Journal of Organic Chemistry|January 17, 2004
Molybdenum-catalyzed stannylations as key steps in heterocyclic synthesisSascha Braune, Matthias Pohlman, Uli KazmaierThe Journal of Organic Chemistry|December 10, 2016
Stereoselective Peptide Modifications via β-C(sp3)-H ArylationsBiplab Mondal, Brindaban Roy, Uli KazmaierThe Journal of Organic Chemistry|September 25, 2004
Allylic alkylation versus Michael induced ring closure: chelated enolates as versatile nucleophilesMatthias Pohlman, Uli Kazmaier, Thomas LindnerMarine Drugs|October 26, 2022
Total Synthesis and Biological Evaluation of Modified Ilamycin DerivativesJennifer Greve, Axel Mogk, Uli KazmaierMethods in Molecular Biology (Clifton, N.J.)|October 1, 2021
Three Methods for the Solution Phase Synthesis of Cyclic PeptidesAngelika Ullrich, Lukas Junk, Uli KazmaierBeilstein Journal of Organic Chemistry|October 7, 2011
A straightforward approach towards combined α-amino and α-hydroxy acids based on Passerini reactionsAmeer F Zahoor, Sarah Thies, Uli KazmaierChemical Communications (Cambridge, England)|July 12, 2002
Synthesis of amino acid derivatives via enantio- and diastereoselective Pd-catalyzed allylic substitutions with a non-stabilized enolate as nucleophileThomas D Weiss, Günter Helmchen, Uli KazmaierChemmedchem|September 3, 2025
Synthesis of a Conformationally Fixed Bicyclomarin DerivativeJennifer Greve, Alexander F Kiefer, Uli KazmaierPageof 14