Alpha-Azidoalkohole und andere kurzlebige Azide

• Antragsteller: Professor Dr. Klaus Banert (†)
• Fachliche Zuordnung: Organische Molekülchemie - Synthese, Charakterisierung
• Förderung: Förderung von 2008 bis 2017
• Projektkennung: Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 81098143

• Erstellungsjahr: 2017

Zusammenfassung der Projektergebnisse

Keine Zusammenfassung vorhanden

Projektbezogene Publikationen (Auswahl)

• Reactions of Unsaturated Azides, Part 29. Experimental and Theoretical Studies on the Synthesis, Spectroscopic Data, and Reactions of Formyl Azide, Angew. Chem. 2012, 124, 4796–4800; Angew. Chem. Int. Ed. 2012, 51, 4718–4721
  K. Banert, C. Berndt, M. Hagedorn, H. Liu, T. Anacker, J. Friedrich, G. Rauhut
  
• Extremely Simple but Long Overlooked: Generation of α-Azido Alcohols by Hydroazidation of Aldehydes, Angew. Chem. 2010, 122, 10404–10407; Angew. Chem. Int. Ed. 2010, 49, 10206–10209
  K. Banert, C. Berndt, S. Firdous, M. Hagedorn, Y.-H. Joo, T. Rüffer, H. Lang
  
• Reactions of Unsaturated Azides, Part 30. 1-Azido-1-alkynes: Synthesis and Spectroscopic Characterization of Azidoacetylene, Angew. Chem. Int. Ed. 2012, 51, 7515–7518
  K. Banert, R. Arnold, M. Hagedorn, P. Thoss, A. A. Auer
  
• Azidoacetylene – interpretation of gas phase infrared spectra based on high-level vibrational configuration interaction calculations, Phys. Chem. Chem. Phys. 2013, 15, 6719–6725
  D. Oschetzki, X. Zeng, H. Beckers, K. Banert, G. Rauhut
  (Siehe online unter https://doi.org/10.1039/c3cp50268f)
• Formyl Azide: Properties and Solid-State Structure, Angew. Chem. 2013, 125, 3587–3591; Angew. Chem. Int. Ed. 2013, 52, 3503–3506
  X. Zeng, E. Bernhardt, H. Beckers, K. Banert, M. Hagedorn, H. Liu
  
• Reactions of Unsaturated Azides, Part 32. Well Known or New? Synthesis and Structure Assignment of Binary C2N14 Compounds Reinvestigated, Angew. Chem. 2013, 125, 3583–3586; Angew. Chem. Int. Ed. 2013, 52, 3499–3502
  K. Banert, S. Richter, D. Schaarschmidt, H. Lang
  
• The Photochemical and Thermal Decomposition of Azidoacetylene in the Gas Phase, Solid Matrix, and Solutions, Eur. J. Org. Chem. 2014, 4077–4082
  X. Zeng, H. Beckers, J. Seifert, K. Banert
  (Siehe online unter https://doi.org/10.1002/ejoc.201402153)
• Reactions of Unsaturated Azides, Part 34. Rearrangement Reactions of Tritylcarbenes: Surprising Ring Expansion and Computational Investigation, Chem. Eur. J. 2015, 21, 14911–14923
  K. Banert, M. Hagedorn, T. Pester, N. Siebert, C. Staude, I. Tchernook, K. Rathmann, O. Hollóczki, J. Friedrich
  (Siehe online unter https://doi.org/10.1002/chem.201501352)
• Synthesis, Characterization and Reactions of (Azidoethynyl)trimethylsilane, Molecules 2015, 20, 21328–21335
  K. Banert, M. Hagedorn, Z. Wu, X. Zeng
  (Siehe online unter https://doi.org/10.3390/molecules201219770)
• The Chemistry of Unusually Functionalized Azides (Review), Synthesis 2016, 48, 2361–2375
  K. Banert
  (Siehe online unter https://doi.org/10.1055/s-0035-1561454)
• Direct observation and characterisation of 3-azido-2H-azirines: postulated, but highly elusive intermediates, Org. Chem. Front. 2017, 4, 191−195
  K. Weigand, N. Singh, M. Hagedorn, K. Banert
  (Siehe online unter https://doi.org/10.1039/c6qo00625f)
• Synthesis of Geminal Azido−Halo Compounds and α-Azidoalkyl Esters from Aldehydes via α-Azido Alcohols, Org. Lett. 2017, 19, 4900−4903
  K. Banert, C. Berndt, K. Weigand
  (Siehe online unter https://doi.org/10.1021/acs.orglett.7b02380)