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Organic synthesis with the most abundant transition metal–iron: from rust to multitasking catalysts. Sujoy Rana, Jyoti Prasad Biswas, Sabarni Paul, Aniruddha Paik, Debabrata Maiti , Chem. Soc. Rev. , 2021 , 50 , 243

The structure of molten mixtures of iron(III) chloride with caesium chloride. G. A. Voyiatzis, A. G. Kalampounias, G. N. Papatheodorou , Phys. Chem. Chem. Phys. , 1999 , 1 , 4797

A new and environmentally benign synthesis of aroylguanidines using iron trichloride. Simon Pape, Pablo Wessig, Heiko Brunner , RSC Adv. , 2015 , 5 , 101408

Non-toxic catalysts for ring-opening polymerizations of biodegradable polymers at room temperature for biohybrid materials. Cordula S. Hege, Stefan M. Schiller , Green Chem. , 2014 , 16 , 1410

Dye-stimulated control of conducting polypyrrole morphology. Stanislav Valtera, Jan Prokeš, Jitka Kopecká, Martin Vrňata, Miroslava Trchová, Martin Varga, Jaroslav Stejskal, Dušan Kopecký , RSC Adv. , 2017 , 7 , 51495

Synthesis and photochromic properties of benzofuran–phenanthrene and benzofuran–pyrene hybrids. H. Surya Prakash Rao, Satish Vijjapu , RSC Adv. , 2014 , 4 , 25747

Chemistry of 9,10-phenanthrenequinone revisited: iron(iii) chloride catalyzed reactions of 9,10-phenanthrenequinone with acyclic and cyclic ketones provide furan annulated products. H. Surya Prakash Rao, Satish Vijjapu , RSC Adv. , 2012 , 2 , 6773

Polypyrrole nanotubes: mechanism of formation. Jitka Kopecká, Dušan Kopecký, Martin Vrňata, Přemysl Fitl, Jaroslav Stejskal, Miroslava Trchová, Patrycja Bober, Zuzana Morávková, Jan Prokeš, Irina Sapurina , RSC Adv. , 2014 , 4 , 1551

Picoloyl protecting group in synthesis: focus on a highly chemoselective catalytic removal. Scott A. Geringer, Michael P. Mannino, Mithila D. Bandara, Alexei V. Demchenko , Org. Biomol. Chem. , 2020 , 18 , 4863

Iron(iii) chloride in oxidative C–C coupling reactions. Abdelwareth A. O. Sarhan, Carsten Bolm , Chem. Soc. Rev. , 2009 , 38 , 2730