The mechanism of the cyclization of meso-(1-hydroxy-2-propenyl)octaethylpor
phyrin to octaethylbenzochlorin is proposed. Chlorin intermediates were iso
lated, characterized and then converted to octaethylbenzochlorin. A rhodino
benzochlorin was isolated on demetallation of Ni coprobenzochlorin with met
hane sulfonic acid and its structure was confirmed by X-ray crystallography
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