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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
Citation: 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.
URI: http://hdl.handle.net/1942/10837
DOI: 10.1021/jo902709c
ISI #: 000275379200048
ISSN: 0022-3263
Category: A1
Type: Journal Contribution
Validation: ecoom, 2011
Appears in Collections: Research publications

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