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Top, S., Vessiéres, A., Leclercq, G., Quivy, J., Tang, J., Vaissermann, J., Huché, M. and Jaouen, G. (2003) Synthesis, Biochemical Properties and Molecular Mod-elling Studies of Organometallic Specific Estrogen Receptor Modulators (SERMs), the Ferrocifens and Hydroxyferrocifens: Evidence for an Antiproliferative Effect of Hydroxyferrocifens on both Hormone-Dependent and Hormone-Independent Breast Cancer Cell Lines. Chemistry: A European Journal, 9, 5223-5236.
http://dx.doi.org/10.1002/chem.200305024

has been cited by the following article:

• TITLE: Synthesis and Structure of Ferrocenol Esters

  AUTHORS: Mikhail Denisov, Aleksey Gorbunov, Maksim V. Dmitriev, Pavel Slepukhin, Vladimir Glushkov

  KEYWORDS: Hydroxyferrocene, Ferroceneboronic Acid, N-Heterocyclic Carbene, Esterification, Catalysis

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.6 No.2, May 31, 2016

  ABSTRACT: N-Heterocyclic carbene-catalyzed oxidative esterification of ferroceneboronic acid by aromatic and heteroaromatic aldehydes affords the new ferrocenol hetaryl and aryl esters 1 - 4, 6 - 8 and 9 - 11. The reaction takes place under mild conditions. The X-ray crystal structure of ferrocenyl esters 3, 6, 11 was determined.