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

Show full item record

SCOPUSTM   
Citations

34
checked on Sep 3, 2020

WEB OF SCIENCETM
Citations

35
checked on May 21, 2022

Page view(s)

12
checked on May 23, 2022

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.