meso-Pyrimidinyl-Substituted A(2)B- and A(3)-Corroles

Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/10837

Title:	meso-Pyrimidinyl-Substituted A(2)B- and A(3)-Corroles
Authors:	Ngo, Thien H. Nastasi, Francesco Puntoriero, Fausto Campagna, Sebastiano Dehaen, Wim MAES, Wouter
Issue Date:	2010
Publisher:	AMER CHEMICAL SOC
Source:	JOURNAL OF ORGANIC CHEMISTRY, 75(6). p. 2127-2130
Abstract:	A variety of meso-pyrimidinyl-substituted A(2)B- and A(3)-corroles (A = 4,6-dichloropyrimidin-5-yl) have been synthesized by careful optimization of the macrocyclization conditions. meso-Pyrimidinylcorroles offer the distinct advantage of an unprecedented broad scope of functionalization options. Highly sterically encumbered triarylcorroles were readily prepared via efficient nucleophilic aromatic Substitution and Suzuki cross-coupling procedures.
Notes:	[Ngo, Thien H.; Dehaen, Wim; Maes, Wouter] Katholieke Univ Leuven, Dept Chem, B-3001 Louvain, Belgium. [Nastasi, Francesco; Puntoriero, Fausto; Campagna, Sebastiano] Univ Messina, Dipartimento Chim Inorgan Chim Analit & Chim Fis, I-98166 Messina, Italy. [Maes, Wouter] Hasselt Univ, Inst Mat Res IMO, Res Grp Organ & Biopolymer Chem, B-3590 Diepenbeek, Belgium.
Document URI:	http://hdl.handle.net/1942/10837
ISSN:	0022-3263
e-ISSN:	1520-6904
DOI:	10.1021/jo902709c
ISI #:	000275379200048
Category:	A1
Type:	Journal Contribution
Validations:	ecoom 2011
Appears in Collections:	Research publications

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