@article {3850,
	title = {Porphyrins bearing halogens at the meso-phenyl and beta-pyrrolic positions: Synthesis and spectral properties},
	journal = {Bulletin De La Societe Chimique De France},
	volume = {133},
	number = {7-8},
	year = {1996},
	note = {ISI Document Delivery No.: VN339Times Cited: 27Cited Reference Count: 58},
	pages = {765-775},
	type = {Article},
	abstract = {The synthesis of symmetrical porphyrins chlorinated at both ortho positions of the meso-aryl substituents, and the chlorination and bromination of the beta-pyrrole positions is reported. The beta-chlorination of meso-tetraphenylporphyrin via its nickel(II) complex is also described. In addition, we communicate the first perchlorination of tetramesitylporphyrin, where halogen substitution occurred at the beta-pyrrolic positions as well as at both the vacant meta positions of the trimethylphenyl groups. The iron complexes of these various polyhalogenated porphyrins are also described, since they are robust and efficient catalysts in oxidation reactions.},
	keywords = {6-dichlorophenyl) porphyrin, bromination, CATALYST, CHLORINATION, COMPLEXES, EASY ACCESS, EFFICIENT CATALYSTS, EPOXIDATION, home, iron porphyrin, IRON(III) PORPHYRINS, METALLOPORPHYRIN, METALLOPORPHYRINS, OXIDATION, SELECTIVE AIR-OXIDATION, TETRAARYLPORPHYRINS, tetrakis(2, TETRAMESITYLPORPHYRIN, TETRAPHENYLPORPHYRINS},
	isbn = {0037-8968},
	url = {<Go to ISI>://A1996VN33900018},
	author = {Wijesekera, T. and Dupre, D. and Cader, M. S. R. and Dolphin, D.}
}
@article {3287,
	title = {Iron porphyrin catalyzed oxidation of lignin model compounds: Oxidation of phenylpropane and phenylpropene model compounds},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {73},
	number = {12},
	year = {1995},
	note = {ISI Document Delivery No.: TV232Times Cited: 4Cited Reference Count: 41},
	month = {Dec},
	pages = {2153-2157},
	type = {Article},
	abstract = {The oxidation of 1-(4-ethoxy-3-methoxyphenyl)propane (2) and 1-(4-ethoxy-3-methoxyphenyl)propene (3) by meso-tetra(2,6-dichloro-3-sulphonatophe)porphyrin iron chloride (TDCSPPFeCl, 1) and tert-butylhydroperoxide (t-BuOOH) are discussed. In addition to a C-alpha-hydroxylation product, demethoxylation and direct aromatic ring cleavage products were found in the oxidation of 2. When 3 was oxidized by 1 and t-BuOOH in aqueous acetonitrile, an acetonitrile-incorporated product was found. A mechanism for the oxidation of 3 is proposed.},
	keywords = {AROMATIC RING CLEAVAGE, BASIDIOMYCETE PHANEROCHAETE-CHRYSOSPORIUM, C BOND-CLEAVAGE, CHARACTERIZATION, DEGRADATION, DEGRADING ENZYME, DIARYLPROPANE, HEME-ENZYME, iron porphyrin, LIGNIN, ligninase, MODEL, OXYGENASE, POTASSIUM MONOPERSULFATE, SPECTRAL, VERATRYL ALCOHOL, WHITE ROT BASIDIOMYCETE},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1995TV23200008},
	author = {Cui, F. and Dolphin, D.}
}
