Anne Christina Staubitz

Affiliations: 
2010-2015 Christian-Albrechts-Universität zu Kiel, Kiel, Schleswig-Holstein, Germany 
 2015- Universität Bremen, Bremen, Bremen, Germany 
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"Anne Staubitz"
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Publications

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Di Tommaso EM, Walther M, Staubitz A, et al. (2023) -Functionalization of azobenzenes hypervalent iodine reagents. Chemical Communications (Cambridge, England). 59: 5047-5050
Li S, Eleya N, Staubitz A. (2020) Cross-Coupling Strategy for the Synthesis of Diazocines. Organic Letters
Eleya N, Appiah C, Lork E, et al. (2020) Synthesis and Thermal Investigations of Eleven-Membered Ring Systems Containing One of the Heavier Group 14 Element Atoms Si, Ge, and Sn. Molecules. 25: 283
Appiarius Y, Stauch T, Lork E, et al. (2020) From a 1,2-azaborinine to large BN-PAHs via electrophilic cyclization: synthesis, characterization and promising optical properties Organic Chemistry Frontiers
Dowds M, Bank D, Strueben J, et al. (2020) Efficient reversible photoisomerisation with large solvodynamic size-switching of a main chain poly(azobenzene-alt-trisiloxane) Journal of Materials Chemistry C. 8: 1835-1845
Hoffmann J, Kuczmera TJ, Lork E, et al. (2019) Synthesis and crystal structure of (E)-1,2-bis-[2-(methyl-sulfan-yl)phen-yl]diazene. Acta Crystallographica Section E: Crystallographic Communications. 75: 1808-1811
Urrego-Riveros S, Ramirez Y Medina IM, Duvinage D, et al. (2019) Negishi's Reagent Versus Rosenthal's Reagent in the Formation of Zirconacyclopentadienes. Chemistry (Weinheim An Der Bergstrasse, Germany)
Hoffmann J, Kuczmera TJ, Lork E, et al. (2019) Synthesis, Structure, Thermal Behavior and cis/trans Isomerization of 2,2′-(EMe3)2 (E = C, Si, Ge, Sn) Substituted Azobenzenes Molecules. 24: 303
Urrego-Riveros S, Bremer M, Hoffmann J, et al. (2019) Conjugated oligomers with alternating heterocycles from a single monomer: synthesis and demonstration of electroluminescence Organic Chemistry Frontiers. 6: 3636-3643
Ramirez Y Medina IM, Rohdenburg M, Mostaghimi F, et al. (2018) Tuning the Optoelectronic Properties of Stannoles by the Judicious Choice of the Organic Substituents. Inorganic Chemistry
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