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β-Functionalized zinc(II)aminoporphyrins by direct catalytic hydrogenation

Authors :
Lipińska, Monika E.
Teixeira, Dalila M.D.
Laia, Cesar A.T.
Silva, Ana M.G.
Rebelo, Susana L.H.
Freire, Cristina
Source :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry. Jan2013, Vol. 54 Issue 1, p110-113. 4p.
Publication Year :
2013

Abstract

Abstract: We report on a novel synthetic procedure to obtain β-aminoporphyrins with zinc(II) as the metal center by using the catalytic reduction of the parent Zn(II)β-nitroporphyrins with hydrogen in the presence of Pd/C using dimethylformamide as the solvent. This simple method allows the preparation of β-aminoporphyrins with substituents with diverse electronic properties: meso-tetraphenylporphyrin (TPP), meso-tetrakis(2,6-dichlorophenyl)porphyrin (TDCPP), and meso-tetrakis(2,3,4,5,6-pentafluorophenyl)porphyrin (TPFPP). [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00404039
Volume :
54
Issue :
1
Database :
Academic Search Index
Journal :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
Publication Type :
Academic Journal
Accession number :
83869577
Full Text :
https://doi.org/10.1016/j.tetlet.2012.10.117