Abstract
1. 1. Methods for introduction of methyl groups into the meso positions of porphyrins and chlorins are described. 2. 2. Acetoxymethyl groups at the meso positions of porphyrins and chlorins are shown to be highly reactive towards nucleophiles. 3. 3. A partial synthesis of a methyl pheophorbide related to bacteriochlorophyll-c is described.
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