Project Details
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Cycloaddition Reactions of Active Cyclic Frustrated Lewis Pairs

Subject Area Organic Molecular Chemistry - Synthesis and Characterisation
Inorganic Molecular Chemistry - Synthesis and Characterisation
Term from 2018 to 2021
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 411668360
 
Final Report Year 2021

Final Report Abstract

No abstract available

Publications

  • Aggregation Behavior of a Six-Membered Cyclic Frustrated Phosphane/Borane Lewis Pair: Formation of a Supramolecular Cyclooctameric Macrocyclic Ring System, Angew. Chem. Int. Ed. 2019, 58, 882-886
    X. Jie, C. G. Daniliuc, R. Knitsch, M. R. Hansen, H. Eckert, S. Ehlert, S. Grimme, G. Kehr, G. Erker
    (See online at https://doi.org/10.1002/anie.201811873)
  • A rare olefin 1,1-carboboration reaction opens a synthetic pathway to an unusually structured frustrated Lewis pair, Chem. Commun. 2020, 56, 8806-8809
    C. Chen, C. G Daniliuc, C. Mück-Lichtenfeld, G. Kehr, G. Erker
    (See online at https://doi.org/10.1039/D0CC01255F)
  • Cycloaddition Reactions of an Active Cyclic Phosphane/Borane Pair with Alkenes, Alkynes, and Carbon Dioxide, Chem. Eur. J. 2020, 26, 1269-1273
    X. Jie, Q, Sun, C. G Daniliuc, R. Knitsch, M. R. Hansen, H. Eckert, G. Kehr, G. Erker
    (See online at https://doi.org/10.1002/chem.201905171)
  • Using the FpXylBH2·SMe2 reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes, Chem. Commun. 2020, 56, 12178-12181
    K. Škoch, C. G Daniliuc, G. Kehr, G. Erker
    (See online at https://doi.org/10.1039/d0cc05230b)
  • Substituent dependent cyclization reactions of 1,1’-bis(alkynyl)ferrocenes with the (C6F5)BH2⋅ SMe2 hydroboration reagent, Eur. J. Inorg. Chem. 2021
    K. Škoch, C. G. Daniliuc, G. Kehr, G. Erker
    (See online at https://doi.org/10.1002/ejic.202100838)
  • The Bis(µ6-benzene)lithium Cation: A Fundamental Main-Group Organometallic Species, Angew. Chem. Int. Ed. 2021, 60, 22879-22884
    X. Jie, J. Li, C. G. Daniliuc, A.-L. Wübker, M. R. Hansen, H. Eckert, C. Mück-Lichtenfeld, G. Kehr, G. Erker
    (See online at https://doi.org/10.1002/anie.202108376)
 
 

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