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Collect. Czech. Chem. Commun. 2004, 69, 330-338
https://doi.org/10.1135/cccc20040330

Synthesis of New Chiral 1,2-Disubstituted Ferrocenes

Ivana Fleischer and Štefan Toma*

Department of Organic Chemistry, Faculty of Natural Sciences, Comenius University, SK-842 15 Bratislava, Slovakia

Crossref Cited-by Linking

  • Mazzeo Giuseppe, Pedotti Sonia, Longhi Giovanna, Patti Angela, Abbate Sergio: Spectroscopic investigation on 1,2-substituted ferrocenes with only planar chirality: How chiroptical data are related to absolute configuration and to substituents. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 2022, 272, 121010. <https://doi.org/10.1016/j.saa.2022.121010>
  • Honegger Philipp, Widhalm Michael: Formaldehyde-1,1″-(phenylphosphinidenesulfide)bis[(2S)-2-[(1R)-1-(methylamino)-ethyl]]ferrocene-aminal. Molbank 2019, 2019, M1090. <https://doi.org/10.3390/M1090>
  • Schaarschmidt Dieter, Lang Heinrich: Selective Syntheses of Planar-Chiral Ferrocenes. Organometallics 2013, 32, 5668. <https://doi.org/10.1021/om400564x>
  • Zirakzadeh Afrooz, Schuecker Raffael, Weissensteiner Walter: Synthesis of chiral, non-racemic ferrocene derivatives by ortho-metallation and partial reductive removal of ortho-directing amino groups. Tet Asymm 2010, 21, 1494. <https://doi.org/10.1016/j.tetasy.2010.03.029>
  • García Jasón, Moyano Albert, Rosol Malgorzata: An efficient, general synthesis of racemic 2-substituted ferrocenecarboxaldehydes. Tetrahedron 2007, 63, 1907. <https://doi.org/10.1016/j.tet.2007.01.003>
  • Steurer Marianne, Wang Yaping, Mereiter Kurt, Weissensteiner Walter: Bromide-Mediated ortho-Deprotonation in the Synthesis of Chiral, Nonracemic Ferrocene Derivatives. Organometallics 2007, 26, 3850. <https://doi.org/10.1021/om7003282>
  • Fleischer Ivana, Toma Stefan: Synthesis of New Chiral 1,2‐Disubstituted Ferrocenes. ChemInform 2004, 35. <https://doi.org/10.1002/chin.200428182>