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