Home Halodiazoacetates as useful tools for selective halo-functionalization
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Halodiazoacetates as useful tools for selective halo-functionalization

  • Hanne Therese Bonge and Tore Hansen
Published/Copyright: January 31, 2011

Online erschienen: 2011-1-31
Erschienen im Druck: 2011-1-31

© 2013 Walter de Gruyter GmbH, Berlin/Boston

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  1. Preface
  2. New methods for the synthesis of certain alkaloids and terpenoids
  3. Synthetic studies toward the spiroimine unit of the spirolides
  4. Chirospecific synthesis: Catalysis and chiral pool hand in hand
  5. Fumonisin: A template for methodology development and drug discovery
  6. 1,5-Polyols: Challenging motifs for configurational assignment and synthesis
  7. Improved synthesis of Bn5CpRu(CO)2Cl and its application as racemization catalyst in preparative-scale metalloenzymatic dynamic kinetic resolution of 1-phenylethanol
  8. Synthesis of mycalazol and mycalazal analogs with potent antiproliferating activities
  9. Development of transition-metal-catalyzed cycloaddition reactions leading to polycarbocyclic systems
  10. New samarium diiodide-induced cyclizations
  11. Fun with radicals: Some new perspectives for organic synthesis
  12. Enhancement of ruthenium-catalyzed olefin metathesis reactions: Searching for new catalyst or new reaction conditions?
  13. Halodiazoacetates as useful tools for selective halo-functionalization
  14. Rhodium-catalyzed enantioselective intermolecular hydroacylation reactions
  15. Specific conjugate addition to α,β-acetylenic ketones
  16. Enantioselective construction of new chiral cyclic scaffolds using [2 + 2 + 2] cycloaddition
  17. Oxidative decarboxylation of α-amino acids to nitriles using o-iodoxybenzoic acid in aqueous ammonia
  18. Convergent synthesis of new types of stabilized carotenoid compounds
  19. Multicomponent synthesis of polysubstituted γ-butyrolactones under Barbier-like conditions
  20. Rational design of novel ligands for environmentally benign cross-coupling reactions
  21. 2-Substituted agelasine analogs: Synthesis and biological activity, and structure and reactivity of synthetic intermediates
  22. An oxidative carbon–carbon bond-forming reaction proceeds via an isolable iminium ion
  23. Design of frustrated Lewis pair catalysts for metal-free and selective hydrogenation
  24. Nitroxides and nucleic acids: Chemistry and electron paramagnetic resonance (EPR) spectroscopy
  25. Chemical genetics approach to drug discovery by diversity-oriented synthesis (DOS) of peptidomimetics
  26. Selective transformations of cephalostatin analogues
  27. Efficient and green synthesis of new polycyclic procyanidin derivatives via tandem dinucleophilic addition of indolin-2-thiones to flavylium salts
  28. 2-Hydroxypropyl derivatives of 1,2,3-thiadiazole and 1,2,3-triazole: Synthesis and antifungal activity
  29. Synthesis of a rhodanine-based compound library targeting Bcl-XL and Mcl-1
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