Home Imitation and modification of bioactive lead structures via integration of boron clusters
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Imitation and modification of bioactive lead structures via integration of boron clusters

  • Sven Stadlbauer , René Frank , Matthias Scholz , Solveig Boehnke , Verena M. Ahrens , Annette G. Beck-Sickinger and Evamarie Hey-Hawkins
Published/Copyright: May 22, 2012

Online erschienen: 2012-5-22
Erschienen im Druck: 2012-5-22

© 2013 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Preface
  2. A unique, two-component sensing system for fluorescence detection of glucose and other carbohydrates
  3. Frustrated Lewis pairs: Some recent developments
  4. Nucleophilic boron strikes back
  5. Heterometallic cubane-type clusters containing group 13 and 16 elements
  6. Derivatization chemistry of the double-decker dicobalt sandwich ion targeted to design biologically active substances
  7. Catalytic enantioselective transformations of borylated substrates: Preparation and synthetic applications of chiral alkylboronates
  8. Polyhedral borane derivatives: Unique and versatile structural motifs
  9. Imitation and modification of bioactive lead structures via integration of boron clusters
  10. Nanotechnology-driven chemistry of boron materials
  11. Isotope incorporation using organoboranes
  12. Synthesis and oxidation of hexafluoroisopropoxyborylferrocenes
  13. Identification of heat shock protein 60 as the regulator of the hypoxia-inducible factor subunit HIF-1α
  14. (2R,3R)-1,4-Dimethoxy-1,1,4,4-tetraphenylbutane-2,3-diol: Valuable reagent in the asymmetric synthesis of organoboronates
  15. Boron-based pronucleophiles in catalytic (asymmetric) C(sp3)–allyl cross-couplings
  16. Complexity-generating hydration reactions via gold-catalyzed addition of boronic acids to alkynes
  17. Progress toward red and near-infrared (NIR) emitting saccharide sensors
  18. Boron and carbon: Antagonistic or complementary? Proposal for a simple prototype of a molecular clutch or molecular switch
  19. Using halo (het) arylboronic species to achieve synthesis of foldamers as protein–protein interaction disruptors
  20. Carbohydrate biomarker recognition using synthetic lectin mimics
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