Synlett, Table of Contents ACCOUNT © Georg Thieme Verlag Stuttgart ˙ New York Corrole: The Little Big Porphyrinoid Roberto Paolesse*Dipartimento di Scienze e Tecnologie Chimiche, Università di Roma ‘Tor Vergata’, Via della Ricerca Scientifica 1, 00133 Rome, ItalyFax: +39(06)72594328; e-Mail: roberto.paolesse@uniroma2.it; Recommend Article Abstract Buy Article All articles of this category Abstract In this account, the author describes the synthetic efforts of his group on the preparation and functionalization of corrole derivatives. The work started with β-alkylcorroles and continued with the preparation of 5,10,15-triarylcorroles. The peripheral functionalization of both the β-alkyl- and meso-triarylcorroles is described, together with several examples of the intriguing and unexpected reactivity of this deceptive macrocycle in these reactions. 1 Introduction 2 Starting with β-Alkylcorroles 3 meso-Substituted Corroles 4 Peripheral Functionalization of Corroles 4.1 Formylation 4.2 Bromination 4.3 Nitration 4.4 Demetalation 5 Isocorroles 6 Remarks and Future Work Key words corroles - porphyrinoids - tetrapyrroles - functionalization - complexes Full Text References References 1 Johnson AW. Kay IT. J. Chem. Soc. 1965, 1620 2 Grigg R. In The Porphyrins Vol. II: Dolphin D. Academic; New York: 1978. p.327 3 Dolphin D. Johnson AW. Leng J. Van Den Broek P. J. Chem. Soc. C 1966, 880 4 Paolesse R. Jaquinod L. Nurco DJ. Mini S. Sagone F. Boschi T. Smith KM. Chem. Commun. 1999, 1307 5 Gross Z. Galili N. Saltsman I. Angew. Chem. Int. Ed. 1999, 38: 1427 6a Paolesse R. In The Porphyrin Handbook Vol. 2: Kadish KM. Smith KM. 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