H. J. Son, W. Wang, T. Xu, Y. Liang, Y. Wu et al., J. Am. Chem. Soc, p.1806, 1885.

Y. Zhou, J. Wang, Z. Gu, S. Wang, W. Zhu et al., Chem. Rev, p.422, 2016.

N. A. Meanwell, J. Med. Chem, p.5822, 2018.

C. Müller, F. Faeh, and . Diederich, Molecules, p.809, 1881.

Z. Zong, W. Jing, J. Shi, S. A. Wen, T. Zhang et al., Antimicrob. Agents Chemother, vol.62, pp.165-183, 2018.

K. B. Dar, A. H. Bhat, S. Amin, R. Hamid, S. Anees et al., Curr. Top. Med. Chem, vol.18, p.2702, 2018.

J. Reymond, R. Van-deursen, L. C. Blum, and L. Ruddigkeit, MedChemComm, 2010.

F. A. Larik, A. Saeed, T. A. Fattah, U. Muqadar, and P. A. Channar, Appl. Organomet. Chem, p.31, 2017.

. Astruc, Eur. J. Inorg. Chem, 2006.

T. J. Colacot-;-b)-r.-gómez-arrayás, J. Adrio, J. C. Carretero-;-c)-v, N. J. Gibson, P. J. Long et al., Angew. Chem. Int. Ed, vol.103, p.615, 1932.

F. W. Grevels, A. Kuran, S. Ozkar, and M. Zora, J. Organomet. Chem, p.122, 1999.

A. Singh, I. Lumb, V. Mehra, and V. Kumar, Dalton Trans, p.2840, 2019.

M. Patra, G. Gasser, ;. Y. Wang, P. M. Dansette, P. Pigeon et al., Nat. Rev. Chem, vol.12, p.70, 2017.

G. Jaouen, A. Vessières, and S. Top, Chem. Soc. Rev, p.8802, 2015.

C. Biot, G. Glorian, L. A. Maciejewski, J. S. Brocard, O. Domarle et al., J. Med. Chem, vol.40, p.730, 1997.

A. Kondratskyi, K. Kondratska, F. Vanden-abeele, D. Gordienko, C. Dubois et al., , 2017.

F. L. Hedberg and H. Rosenberg, J. Organomet. Chem, p.14, 1971.

H. Butenschön, Synthesis, vol.50, p.3787, 2018.

J. H. Peet and B. W. Rockett, J. Organomet. Chem, p.57, 1974.

K. Sünkel and S. Weigand, Inorg. Chim. Acta, 2011.

K. Sünkel, S. Weigand, A. Hoffmann, S. Blomeyer, C. G. Reuter et al., J. Am. Chem. Soc, vol.137, issue.126, 2015.

J. Metzler-nolte, . Organomet, . S. Chem-;-m, S. Inkpen, M. Du et al., Organometallics, vol.797, p.5461, 2015.

H. Butenschön and G. Werner, Eur. J. Inorg. Chem, p.378, 2017.

C. J. Richards, A. J. Locke-;-b)-r, V. C. Atkinson, N. J. Gibson, . R. Long-;-i et al., Concerning deprotometalation-trapping in the ferrocene series, vol.9, p.5668, 1998.

S. Gronowitz-;-b, ). G. Queguiner, F. Marsais, V. Snieckus, J. Epsztajn et al., Concerning studies on fluorine-free ferrocenes, vol.14, p.3820, 1161.

M. Tazi, W. Erb, Y. S. Halauko, O. A. Ivashkevich, V. E. Matulis et al., Organometallics, vol.36, p.2862, 2010.

M. Tazi, M. Hedidi, W. Erb, Y. S. Halauko, O. A. Ivashkevich et al., Organometallics, p.9132, 2018.

R. Sanders and U. T. Mueller-westerhoff, J. Organomet. Chem, p.219, 1996.

C. F. Lavey, D. Hesk, S. Hendershot, D. Koharski, S. Saluja et al., J. Labelled Compd. Radiopharm, p.264, 2007.

D. Haas, J. M. Hammann, R. Greiner, and P. Knochel, Angew. Chem., Int. Ed, p.6738, 1540.

N. Brikci-nigassa, G. Bentabed-ababsa, W. Erb, and F. Mongin, Synthesis, vol.50, p.3615, 2018.

F. Mongin, C. Curty, E. Marzi, F. R. Leroux, and M. Schlosser, ARKIVOC, p.48, 2015.

, While it similarly proved impossible to isolate and characterize the ferrocene carboxaldehydes coming from 3p-Br and 3p-I due to their instability, the product formed from 3p-Cl (2,4-dichloro-3-fluoroferrocenecarboxaldehyde (5p-Cl); see ESI) was fully characterized by NMR before its degradation

B. Ferber, S. Top, R. Welter, and G. Jaouen, Chem. Eur. J, 2006.