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Locked pi-expanded chlorins in two steps from simple tetraarylporphyrins
Authors:Fouchet Julien  Jeandon Christophe  Ruppert Romain  Callot Henry J
Institution:U.M.R. 7177 du C.N.R.S., Faculté de Chimie, Université Louis Pasteur, 1, Rue Blaise Pascal, F-67000 Strasbourg, France.
Abstract:reaction: see text] Upon tandem Reformatsky reaction, easily accessible porphyrinic ketones give "locked" chlorinic diester. Both ketones and diesters, as bases or palladium complexes, efficiently generate singlet dioxygen, as demonstrated by trapping with cholesterol.
Keywords:
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